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IGA

IGA v2.1

IGA NovaSeq Sequencing v2.1

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Overview

IGA NovaSeq Sequencing v2.1 contains preset protocols that support the setup of previously prepared libraries used with the NovaSeq instrument. These protocols can be used with the IGA Library Prep Automated v2.1 workflow. They also provide the following functions:

  • File-based integration with the Hamilton robots that are used for liquid handling steps.

  • Automated calculation of sample and buffer volumes.

  • Automated calculation or display of reagents.

  • When required, automatic step transition.

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Protocol 1: Run Format (IGA)

Protocol Type = Library Prep

Next Steps Configuration

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Step 1: Define Run Format (IGA)

  • Master Step Name = Define Run Format (IGA v2.1)

  • Step Type = No Outputs

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Automations

chevron-rightRegister Sample & Register Step Started (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightDefine Run Format - Assign Workflow and Flowcell Type to Samples & Set Next Steps to Remove from Workflow (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightDefine Run Format - Routing Script (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Record Details

  • Step Data (Master Step Fields)

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Protocol 2: NovaSeq Standard

Protocol Type = Library Prep

Next Steps Configuration

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Step 1: Make Bulk Pool for NovaSeq Standard

  • Master Step Name = Make Bulk Pool for NovaSeq Standard (IGA v2.1)

  • Step Type = Pooling

  • Aliquot Generation = Fixed, 1

  • Naming Convention = {PoolName}

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Automations

chevron-rightRegister Sample & Register Step Started (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightPooling NovaSeq Standard - Show Warning Message (IGA v2.1)hashtag
  • Trigger Location = Pooling

  • Trigger Style = Automatic upon entry

chevron-rightValidate Inputs Flowcell Type and Number of Pools (IGA v2.1)hashtag
  • Trigger Location = Pooling

  • Trigger Style = Automatic upon exit

chevron-rightNovaSeq Make Bulk Pool - Output Plate BPP Barcode Check (Duplicates Allowed) (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon exit

chevron-rightMake Bulk Pool NovaSeq Standard - Calculate Volumes and Generate Hamilton Input File (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightMake Bulk Pool NovaSeq Standard - Validate Hamilton Output File Name if Present, Parse Instrument ID, Set Next Steps to Advance (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightRegister Step Completed (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

chevron-rightValidate Unique Indexes (IGA v2.1)hashtag
  • Trigger Location = Not Used

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Pooling

  • Label Uniqueness = On

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

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Placement = Enabled

  • Defaults

    • Well Sort Order = Column

    • Placement Pattern = Column

  • Destination Containers

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Record Details

  • Step Data (Master Step Fields)

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Step 2: Dilute and Denature

  • Master Step Name = Dilute and Denature (IGA v2.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

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Automations

chevron-rightValidate Single Input (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightValidate Library Tube Barcode (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon exit

chevron-rightDilute and Denature NovaSeq Standard - Generate Hamilton Library Tube Input File, Validate Run Setup, and Generate SampleSheet (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightDilute and Denature NovaSeq Standard - Set Next Steps to Remove from Workflow (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightDilute and Denature NovaSeq Standard - Routing Script (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

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Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

    • Placement Pattern = Column

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Record Details

  • Step Data (Master Step Fields)

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Protocol 3: NovaSeq Xp

Protocol Type = Library Prep

Next Steps Configuration

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Step 1: Make Bulk Pool for NovaSeq Xp

  • Master Step Name = Make Bulk Pool for NovaSeq Xp (IGA v2.1)

  • Step Type = Pooling

  • Aliquot Generation = Fixed, 1

  • Naming Convention = {PoolName}

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Automations

chevron-rightRegister Sample & Register Step Started (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightValidate Inputs Flowcell Type and Single Pool (IGA v2.1)hashtag
  • Trigger Location = Pooling

  • Trigger Style = Automatic upon exit

chevron-rightNovaSeq Make Bulk Pool - Output Plate BPP Barcode Check (Duplicates Allowed) (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon exit

chevron-rightMake Bulk Pool NovaSeq Xp - Reset Loading Workflow Type and Flowcell Type (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

chevron-rightMake Bulk Pool NovaSeq Xp - Calculate Volumes and Generate Hamilton Input File (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightSet Flowcell Type and Next Step (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightRegister Step Completed (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

chevron-rightValidate Unique Indexes (IGA v2.1)hashtag
  • Trigger Location = Not Used

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Pooling

  • Label Uniqueness = On

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Placement = Enabled

  • Defaults

    • Well Sort Order = Row

    • Placement Pattern = Column

  • Destination Containers

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Record Details

  • Step Data (Master Step Fields)

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Step 2: Dilute, Denature & ExAmp

  • Master Step Name = Dilute, Denature & ExAmp (IGA v2.1)

  • Step Type = Standard

  • Derived Sample Generation = Variable

  • Naming Convention = {InputItemName}_WP{OutputItemNumber}

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Automations

chevron-rightDil/Den/ExAmp NovaSeq Xp - Generate Hamilton Consolidated Bulk Pool MakeBPP Input File and Validate Input Flowcell Type (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightDil/Den/ExAmp NovaSeq Xp - Validate Hamilton BPP Output File Name & Parse Instrument ID (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon entry

chevron-rightDil/Den/ExAmp NovaSeq Xp - Output Plate WPP Barcode Uniqueness Check (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon exit

chevron-rightDil/Den/ExAmp NovaSeq Xp - Calculate Volumes and Generate Incomplete WPP Driver File for Next Step (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

chevron-rightDil/Den/ExAmp NovaSeq Xp - Set Next Steps to Advance (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightRegister Step Completed (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

chevron-rightSet Flowcell Type and Next Step (IGA v2.1)hashtag
  • Trigger Location = Not Used

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Step Setup = Enabled

  • File Placeholders

    1. Hamilton Consolidated MakeBPP Bulk Pool Input File

      • Description = This file contains consolidated Bulk Pool information to run the Hamilton MakeBPP method. It refers to previous Xp Make Bulk Pool steps in Clarity that all use the same BPP output plate name. Please run this file with the Hamilton MakeBPP method before continuing with this step.

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Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

    • Placement Pattern = Column

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Record Details

  • Step Data (Master Step Fields)

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Step 3: Load to Flowcell

  • Master Step Name = Load to Flowcell (IGA v2.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

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Automations

chevron-rightValidate Inputs and Selected Container (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon entry

chevron-rightValidate Flowcell Barcode with New Mask Fixes (IGA v2.1)hashtag
  • Trigger Location = Placement

  • Trigger Style = Automatic upon exit

chevron-rightValidate Run Setup and Generate Sample Sheet (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightLoad to Flowcell NovaSeq Xp - Generate Hamilton WPP Input File (IGA v2.1)hashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightRegister Step Completed (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

chevron-rightValidate Flowcell Barcode (IGA v2.1)hashtag
  • Trigger Location = Not Used

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

    • Placement Pattern = Column

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Record Details

  • Step Data (Master Step Fields)

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Protocol 4: AUTOMATED - NovaSeq Run

Protocol Type = Sequencing

Next Steps Configuration

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Step 1: AUTOMATED - NovaSeq Run

  • Master Step Name = AUTOMATED - NovaSeq Run (IGA v2.1)

  • Step Type = Analysis

  • Measurement Generation = Variable

  • Naming Convention = Lane {OutputItemNumber}

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Automations

chevron-rightRegister Step Completed (IGA v2.1)hashtag
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

chevron-rightSet Next Steps (IGA v2.1)hashtag
  • Trigger Location = Not Used

chevron-rightShow warning message and register step started at AUTOMATED step (IGA v2.1)hashtag
  • Trigger Location = Not Used

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Queue

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

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Record Details

  • Step Data (Master Step Fields)

Column Headers

Category

Field Name

Field Type

Options

Additional Options and Dropdown Items

Container

Container Name

Built-in

Container

Well

Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Step File Placeholders

    • Log file - Automatically attached

  • Sample Table (Table Columns - Global Fields)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

  • Control Types
    • PhiX v3

    Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • 96 well plate

    Liquid Handling Instrument ID

    Text

    Read Only

    Apply Correction Factors

    Text Dropdown

    Required Field

    • Presets

      • None

      • IDPF

      • Custom

    Quick reference checklist: Make Bulk Pool for NovaSeq Standard. i) pre Liquid Handler

    Multiline Text

    Read Only

    • Defaults = User tasks for this page: - Select 'Number Of Flowcells' and 'Min Per Sample Volume (ul)' - 'Run' the Make Bulk Pool automation, and download resulting Hamilton Make Bulk Pool Input File

    Quick reference checklist: Make Bulk Pool for NovaSeq Standard. ii) post Liquid Handler

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    Read Only

    • Defaults = User tasks for this page: - After running MakeBPP on the liquid handler, upload resulting Hamilton Output File - Click on 'Next Steps'

  • Step File Placeholders

    • Calculation Log - Automatically attached

    • Hamilton Make Bulk Pool Input File - Automatically attached

    • Hamilton file log - Automatically attached

    • Hamilton Output File - Manually uploaded

    • Custom Correction Factors - Manually uploaded

    • Index Correction Log - Automatically attached

  • Sample Table (Table Columns - Global Fields)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

  • Reagent Kits
    • NaOH

      • Supplier = Illumina

    • Resuspension Buffer (RSB)

      • Supplier = Illumina

    • Tris-HCl

      • Supplier = Illumina

    Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Destination Containers

    • Library Tube

    BaseSpace App Slug

    Text Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • Illumina-inc.bcl-convert.1.3.0

      • Illumina-inc.bcl-convert.1.2.0

    BaseSpace Sequence Hub Analysis Workflow

    Text

    • Required Field

    • Default = TSS Connect v1.1

    BaseSpace Sequence Hub Configuration

    Text Dropdown

    • Required Field

    • Presets

      • Run Monitoring And Storage

      • Run Monitoring Only

      • Not Used

    BaseSpace Sequence Hub Project Name

    Text

    • Required Field

    Custom Recipe Path

    Text

    Enable Secondary Analysis

    Toggle Switch

    • Required Field

    • Default = Yes

    Experiment Name

    Text

    • Required Field

    Index Read 1

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 10

      • 6

      • 8

    Index Read 2

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 10

      • 6

      • 8

    Liquid Handling Instrument ID

    Text

    • Read Only

    Output Folder

    Text

    • Required Field

    Paired End

    Text Dropdown

    • Required Field

    • Presets

      • True

      • False

    • Default = True

    Quick reference checklist: Dilute and Denature.

    Multiline Text

    • Read Only

    • Defaults = User tasks for this page: - Select NaOH/TrisHCl/RSB lots, and input run configuration - 'Run' Dilute and Denature automation, download resulting input 'Hamilton Load to Library tube file' - Click 'Next Steps' and then 'Finish Step' to move library tube through to 'AUTOMATED - NovaSeq Run'.

    Read 1 Cycles

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 151

      • 251

      • 101

    Read 2 Cycles

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 151

      • 251

      • 101

    Required Yield Gbp

    Numeric

    • Required Field

    • Default = 90

    Run Mode

    Text Dropdown

    • Read Only

    • Presets

      • S4

      • S1

      • S2

    SampleSheet Version

    Text Dropdown

    • Required Field

    • Presets

      • V2

      • V1

    • Default = V2

    Use Custom Index Read 1 Primer

    Toggle Switch

    • Default = No

    Use Custom Read 1 Primer

    Toggle Switch

    • Required Field

    • Default = No

    Use Custom Read 2 Primer

    Toggle Switch

    • Required Field

    • Default = No

    Use Custom Recipe

    Toggle Switch

    • Required Field

    • Default = No

    Workflow

    Text

    • Read Only

    • Default = GenerateFASTQ

    Workflow Type

    Text Dropdown

    • Required Field

    • Presets

      • Dual Index

      • Single Index

      • No Index

  • Step File Placeholders

    • Sample Sheet - Automatically attached

    • Sample sheet Log File - Automatically attached

    • Hamilton Load to Library tube file - Automatically attached

    • Hamilton file log - Automatically attached

    • Biosample Manifest - Automatically attached

  • Sample Table (Table Columns - Global Fields)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • 96 well plate

    Apply Correction Factors

    Text Dropdown

    Required Field

    • Presets

      • None

      • IDPF

      • Custom

    Quick reference checklist: Make Bulk Pool for NovaSeq Xp. i) pre Liquid Handler

    Multiline Text

    Read Only

    • Defaults = User tasks for this page: - Select 'Number Of Lanes' and 'Min Per Sample Volume (ul)' - 'Run' the Make Bulk Pool automation - Click 'Next Steps' and 'Finish Steps'. To add another Bulk Pool to this BPP, repeat Make Bulk Pool for NovaSeq Xp. Once your BPP contains the pools you need, continue on to Dilute and Denature to get the collated MakeBPP Liquid Handler input file.

  • Step File Placeholders

    • Log - Automatically attached

    • Hamilton Make Bulk Pool Input File - Automatically attached

    • Hamilton Input File Generation Log - Automatically attached

    • Custom Correction Factors - Manually uploaded

    • Index Correction Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

  • Reagent Kits
    • DPX1

      • Supplier = Illumina

      • Catalog Number = 20019916

    • DPX2

      • Supplier = Illumina

      • Catalog Number = 20019917

    • DPX3

      • Supplier = Illumina

      • Catalog Number = 20019918

    • NaOH

    • Resuspension Buffer (RSB)

    • Tris-HCl

    Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Attachment = Auto
  • Upload Hamilton MakeBPP Output File

    • Description = Please upload the Hamilton output file from the MakeBPP run.

    • Attachment = Manual

  • Destination Containers

    • 96 well plate

    DPX3 Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 0

    Liquid Handling Instrument ID

    Text

    Read Only

    Quick reference checklist: Dilute, Denature and ExAmp

    Multiline Text

    Read Only

    Defaults = User tasks for this page: - Input DPX/NaOH/RSB/TrisHCl lots - Click 'Next Steps'

  • Step File Placeholders

    • Calculation File - Automatically attached

    • Log File - Automatically attached

    • Incomplete WPP Hamilton Files (DO NOT USE; REQUIRED FOR NEXT STEP!) - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Destination Containers

    • SP

    • S1

    • S2

    • S4

    BaseSpace App Slug

    Text Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • Illumina-inc.bcl-convert.1.3.0

      • Illumina-inc.bcl-convert.1.2.0

    BaseSpace Sequence Hub Analysis Workflow

    Text

    • Required Field

    • Default = TSS Connect v1.1

    BaseSpace Sequence Hub Configuration

    Text Dropdown

    • Required Field

    • Presets

      • Run Monitoring And Storage

      • Run Monitoring Only

      • Not Used

    BaseSpace Sequence Hub Project Name

    Text

    • Required Field

    Custom Recipe Path

    Text

    Enable Secondary Analysis

    Toggle Switch

    • Required Field

    • Default = Yes

    Experiment Name

    Text

    • Required Field

    Index Read 1

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 10

      • 6

      • 8

    Index Read 2

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 10

      • 6

      • 8

    Library Tube Barcode

    Text

    • Required Field

    Output Folder

    Text

    • Required Field

    Paired End

    Text Dropdown

    • Required Field

    • Presets

      • True

      • False

    • Default = True

    Quick reference checklist: Load To Flowcell.

    Multiline Text

    • Read Only

    • Defaults = User tasks for this page: - Populate run configuration settings above - 'Run' Load To Flowcell automation, download resulting 'Hamilton Input File (BPP to WPP to Flow Cell)' file - 'Run' Validate Run Setup and Generate Sample Sheet (IGA v2.1) automation - Click 'Next Steps' and then 'Finish Step' to move flowcell through to 'AUTOMATED - NovaSeq Run'

    Read 1 Cycles

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 151

      • 251

      • 101

    Read 2 Cycles

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 151

      • 251

      • 101

    Required Yield Gbp

    Numeric

    • Default = 90

    SampleSheet Version

    Text Dropdown

    • Required Field

    • Presets

      • V2

      • V1

    • Default = V2

    Use Custom Index Read 1 Primer

    Toggle Switch

    • Required Field

    • Default = No

    Use Custom Read 1 Primer

    Toggle Switch

    • Required Field

    • Default = No

    Use Custom Read 2 Primer

    Toggle Switch

    • Required Field

    • Default = No

    Use Custom Recipe

    Toggle Switch

    • Required Field

    • Default = No

    Workflow

    Text

    • Read Only

    • Default = GenerateFASTQ

    Workflow Type

    Text Dropdown

    • Required Field

    • Presets

      • Dual Index

      • Single Index

      • No Index

  • Step File Placeholders

    • Sample Sheet - Automatically attached

    • Log File - Automatically attached

    • Hamilton Input File (BPP to WPP to Flow Cell) - Automatically attached

    • Biosample Manifest - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

  • Reagent Kits
    • Buffer Cartridge

      • Supplier = Illumina

    • Cluster Cartridge

      • Supplier = Illumina

    • SBS Cartridge

      • Supplier = Illumina

    Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Column Headers

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    Well

    Built-in

  • Expanded View Fields

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    LIMS ID (Container)

    Built-in

    Project

    Project Name

  • Firmware Version

    Text

    Read Only

    Flow Cell Expiration Date

    Date

    Read Only

    Flow Cell ID

    Text

    Read Only

    Flow Cell Lot Number

    Text

    Read Only

    Flow Cell Mode

    Text

    Read Only

    Flow Cell Part Number

    Text

    Read Only

    Flow Cell Side

    Text

    Read Only

    Instrument Control Software Version

    Text

    Read Only

    Instrument ID

    Text

    Read Only

    Instrument Type

    Text

    Read Only

    Loading Workflow Type

    Text

    Read Only

    Output Folder

    Text

    Read Only

    RTA Version

    Text

    Read Only

    Run ID

    Text

    Read Only

    Run Status

    Text

    Read Only

    Sequencing Log

    Multiline Text

    Read Only

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • File Column Options

      • File Column Display = Hide

      • File Attachment Method = Manual

    • Table Columns - Global Fields

  • Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    IGA WF Build Version

    Text

    Read Only

    Default = 2.1.0.1

    Quick reference checklist: Define Run Format.

    Multiline Text

    Read Only

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Number of Flowcells to Sequence

    Numeric

    Required Field

    • Default = 1

    • Range From 1 to 10

    • Decimal Places Displayed = 0

    Minimum Per Sample Volume (ul)

    Numeric

    Required Field

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Adapter

    Text

    • Required Field

    • Default = CTGTCTCTTATACACATCT

    Adapter Read 2

    Text

    • Required Field

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Number of Lanes to Sequence

    Numeric

    Required Field

    • Decimal Places Displayed = 0

    Minimum Per Sample Volume (ul)

    Numeric

    Required Field

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    DPX1 Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 0

    DPX2 Volume (ul)

    Numeric

    Read Only

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Adapter

    Text

    • Required Field

    • Default = CTGTCTCTTATACACATCT

    Adapter Read 2

    Text

    • Required Field

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Current Cycle

    Numeric

    Read Only

    Decimal Places Displayed = 0

    Current Read

    Numeric

    Read Only

    Defaults = User tasks for this page: - Below, assign 'Loading Workflow Type', 'Flowcell Type', and the NovaSeq 'Final Loading Concentration (pM)'. - Click 'Next Steps'.

    • Default = 2

    • Decimal Places Displayed = 2

    • Default = CTGTCTCTTATACACATCT

    • Default = 2

    • Decimal Places Displayed = 2

    Decimal Places Displayed = 0

    • Default = CTGTCTCTTATACACATCT

    Decimal Places Displayed = 0

    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/register_sample.groovy' && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'nextStep = ::REMOVE:: ; input.::Minimum Molarity (nM):: = (5 * input.::Final Loading Concentration (pM)::)/1000 ; if (!input.hasValue(::Normalized Molarity (nM)::)) { fail(::The Normalized Molarity cannot be empty.::) ; } else if (input.::Normalized Molarity (nM):: < input.::Minimum Molarity (nM)::) { input.::Warning:: = ::The Normalized Molarity is too low.:: ; input.::Loading Workflow Type:: = ::[Remove from workflow]:: ; } else { input.::Warning:: = ::n/a:: }' -log {compoundOutputFileLuid0}"
    bash -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_completed.groovy' && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -u {username} -p {password} -i {stepURI:v2} -l {compoundOutputFileLuid0} script:changeWorkflow \
    \
    --FIELD_NAME 'Loading Workflow Type' \
    --FIELD_VALUE 'NovaSeq Standard' \
    --WORKFLOW 'Illumina Genomics Architecture - NovaSeq Sequencing v2.1' \
    --STEP 'Make Bulk Pool for NovaSeq Standard (IGA v2.1)' \
    --INPUTS_OR_OUTPUTS 'INPUTS' \
    \
    --FIELD_NAME 'Loading Workflow Type' \
    --FIELD_VALUE 'NovaSeq Xp' \
    --WORKFLOW 'Illumina Genomics Architecture - NovaSeq Sequencing v2.1' \
    --STEP 'Make Bulk Pool for NovaSeq Xp (IGA v2.1)' \
    --INPUTS_OR_OUTPUTS 'INPUTS'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/register_sample.groovy' && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 \
    /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/NovaSeq_pooling_warning.py \
    -s {stepURI:v2} \
    -u {username} \
    -p {password} \
    -l {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:validate_flowcell_for_input_pools -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -validateSingleOutput false -poolType bulk \
    && PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/validate_flowcell_pools.py -s {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2:http} -u {username} -p {password} script:evaluateDynamicExpression -exp 'if ( !output.container.name.matches( ::LP[0-9]{7}-BPP:: ) ) {fail ( ::Invalid BPP Plate Barcode. This plate ID must be in the format LPxxxxxxx-BPP, where 'x' is a digit 0-9, e.g. LP1234567-BPP. Please verify and try again.:: ) }' -log {compoundOutputFileLuid0} \
    && PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/validate_multiple_destination_plates.py -s {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} -t true -log {compoundOutputFileLuid0} \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'step.::Number of Samples in Pool:: = step.::Number of Samples in Pool:: + 1' \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'if ( input.::Flowcell Type:: == ::SP:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Flowcells to Sequence:: * 100 + 30 } ; if ( input.::Flowcell Type:: == ::S1:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Flowcells to Sequence:: * 100 + 30 } ; if ( input.::Flowcell Type:: == ::S2:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Flowcells to Sequence:: * 150 + 30 } ; if ( input.::Flowcell Type:: == ::S4:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Flowcells to Sequence:: * 310 + 30 } ; input.::Per Sample Volume (ul):: = 0' \
    && PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 \
    /opt/gls/clarity/extensions/IGA_2.1/make_bpp/calculate_sample_volume.py \
    -s {stepURI:v2} \
    -u {username} \
    -p {password} \
    && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} -t true -log {compoundOutputFileLuid0} \
        script:calculate_adjusted_per_sample_volume \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'step.::Total Sample Volume (ul):: = step.::Total Sample Volume (ul):: + input.::Adjusted Per Sample Volume (ul)::' \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'if (step.::Total Sample Volume (ul):: >= step.::Bulk Pool Volume (ul)::) {output.::RSB Volume (ul):: = 0} else {output.::RSB Volume (ul):: = step.::Bulk Pool Volume (ul):: - step.::Total Sample Volume (ul)::} ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type:: ; if ( input.::Flowcell Type:: == ::SP:: ) { output.::Volume of Pool to Denature (ul):: = 100 ; output.::NaOH Volume (ul):: = 25 ; output.::Tris-HCl Volume (ul):: = 25 } ;  if ( input.::Flowcell Type:: == ::S1:: ) { output.::Volume of Pool to Denature (ul):: = 100 ; output.::NaOH Volume (ul):: = 25 ; output.::Tris-HCl Volume (ul):: = 25 } ; if ( input.::Flowcell Type:: == ::S2:: ) {output.::Volume of Pool to Denature (ul):: = 150 ; output.::NaOH Volume (ul):: = 37.50 ; output.::Tris-HCl Volume (ul):: = 37.50 } ; ; if ( input.::Flowcell Type:: == ::S4:: ) { output.::Volume of Pool to Denature (ul):: = 310 ; output.::NaOH Volume (ul):: = 77.50 ; output.::Tris-HCl Volume (ul):: = 77.50 }' \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar \
    -i {stepURI:v2} -u {username} -p {password} -t true -log {compoundOutputFileLuid0} \
    script:evaluateDynamicExpression \
    -h false \
    -exp 'step.::Number of Samples in Pool:: = step.::Number of Samples in Pool:: - 1; step.::Total Sample Volume (ul):: = step.::Total Sample Volume (ul):: - input.::Adjusted Per Sample Volume (ul)::' \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
    script:driver_file_generator \
    -i {stepURI:v2} \
    -u {username} \
    -p {password} \
    -q true \
    -destLIMSID {compoundOutputFileLuid1} \
    -t /opt/gls/clarity/extensions/IGA_2.1/hamilton_fast_prep/templatefiles/MakeBPFile_NovaSeq_template.csv \
    -o Output_plate_name.csv \
    -l {compoundOutputFileLuid2} && \
    PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 \
    /opt/gls/clarity/extensions/IGA_2.1/make_bpp/apply_multiple_bulk_pools.py \
    -s {stepURI:v2} \
    -u {username} \
    -p {password} \
    --min-volume {udf:Minimum Per Sample Volume (ul)} \
    --selected-cf {udf:Apply Correction Factors} \
    --hamilton-limsid {compoundOutputFileLuid1} \
    --custom-cf-limsid {compoundOutputFileLuid4} \
    -l {compoundOutputFileLuid5} "
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'step.::Liquid Handling Instrument ID:: = ::::' -log {compoundOutputFileLuid0} \
    && \
    /usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/01_NovaSeqStd_confirmPlateIDAndStoreInstrumentID_OptionalFile.py -u {username} -p {password} -s {stepURI} -f {compoundOutputFileLuid3} -i 'Liquid Handling Instrument ID' \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'if (!step.hasValue(::Liquid Handling Instrument ID::)) {step.::Liquid Handling Instrument ID:: = ::NO HAMILTON OUTPUT FILE UPLOADED:: } ; nextStep = ::ADVANCE::' -log {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_completed.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/pooling.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:validateUniqueIndexes"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:validateSampleCount -min 1 -max 1 && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -exp 'if (!output.container.name.matches( ::[A-Z]{2}[0-9]{7}-[A-Z]{3}:: ) ) {fail ( ::Invalid Library Tube Barcode. This must be in the format CCxxxxxxx-CCC, where 'x' is a digit 0-9 and 'C' is an uppercase letter, e.g. LP1234567-ABC. Please verify and try again.:: ) } ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type::' -log {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
    script:driver_file_generator \
    -i {stepURI:v2} \
    -u {username} \
    -p {password} \
    -q true \
    -destLIMSID {compoundOutputFileLuid2} \
    -t /opt/gls/clarity/extensions/IGA_2.1/hamilton_fast_prep/templatefiles/LoadToLibTubeFile_NovaSeqStd_template.csv \
    -o Output_plate_name.csv \
    -l {compoundOutputFileLuid3} && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} \
        script:evaluateDynamicExpression \
            -exp 'step.::Run Mode:: = input.::Flowcell Type:: ; if (!step.::Experiment Name::.matches(::[a-zA-Z0-9-_]+::)) { fail(::Experiment Name contains prohibited characters. Allowed characters are: a-z, A-Z, 0-9, -, and _::) }; if (step.::Workflow Type:: == ::No Index::) { if (step.::Index Read 1:: != 0) { fail(::Index Read 1 must be 0 if the Workflow Type is No Index.::) } } else { if (step.::Index Read 1:: == 0) { fail(::Index Read 1 must be greater than 0 if the Workflow Type is :: + step.::Workflow Type:: + ::.::) } }; if (step.::Paired End::.toBoolean() && step.::Read 2 Cycles:: == 0) { fail(::Read 2 Cycles must not be zero if it is Paired End read.::) }; if (step.::Workflow Type:: == ::Dual Index:: && step.::Index Read 2:: == 0) { fail(::Index Read 2 must not be zero if Workflow Type is Dual Index.::) }; if (step.::Workflow Type:: == ::No Index:: || step.::Workflow Type:: == ::Single Index::) { step.::Index Read 2:: = 0 }; if (!step.::Paired End::.toBoolean()) { step.::Read 2 Cycles:: = 0 }; if (input.::Flowcell Type::!=::SP:: && step.::Read 1 Cycles:: > 151) { fail(::Read 1 Cycles must not be larger than 151 if it is not SPrime Flowcell::) };if (input.::Flowcell Type::!=::SP:: && step.::Read 2 Cycles:: > 151) { fail(::Read 2 Cycles must not be larger than 151 if it is not SPrime Flowcell::) }; nextStep = ::REMOVE::' \
            -log {compoundOutputFileLuid1} \
            -t true \
    && if [[ '{udf:SampleSheet Version}' == 'V2' && '{udf:Enable Secondary Analysis}' == 'false' ]]; then \
    templateFilename='/opt/gls/clarity/extensions/IGA_2.1/ss_converter_templates/NovaSeq_BCL2FASTQ_Samplesheet_Std_V2.csv'; \
           else \
    templateFilename='/opt/gls/clarity/extensions/IGA_2.1/ss_converter_templates/NovaSeq_BCL2FASTQ_Samplesheet_Std_V1.csv'; \
    fi \
    && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar -i {stepURI:v2} -u {username} -p {password} \
        script:driver_file_generator \
            -t $templateFilename \
            -o {compoundOutputFileLuid0}.csv \
            -q true \
            -destLIMSID {compoundOutputFileLuid0} \
            -l {compoundOutputFileLuid1} \
    && if [[ '{udf:Enable Secondary Analysis}' == 'true' ]]; then \
    PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 /opt/gls/clarity/extensions/IGA_2.1/ss_converter \
            --input {compoundOutputFileLuid0}.csv  \
            --bssh-app {udf:BaseSpace App Slug} \
            --stepURI {stepURI:v2} -u {username} -p {password} -q \
            --destLIMSID {compoundOutputFileLuid0} 2>&1; \
    fi && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
      -i {stepURI:v2} -u {username} -p {password} \
      script:driver_file_generator \
            -t /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/Biosample_Manifest.csv \
            -o {compoundOutputFileLuid4}.csv \
            -q true \
            -destLIMSID {compoundOutputFileLuid4} \
            -l {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'step.::Liquid Handling Instrument ID:: = ::::' -log {compoundOutputFileLuid1} \
    && \
    /usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/02_NovaSeqStd_confirmPlateIDAndStoreInstrumentID_OptionalFile_DiluteDenature.py -u {username} -p {password} -s {stepURI} -f {compoundOutputFileLuid4} -i 'Liquid Handling Instrument ID' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'if (!step.hasValue(::Liquid Handling Instrument ID::)) {step.::Liquid Handling Instrument ID:: = ::NO HAMILTON OUTPUT FILE UPLOADED:: } ; nextStep = ::REMOVE::' -log {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -u {username} -p {password} -i {stepURI:v2} -l {compoundOutputFileLuid1} script:changeWorkflow \
            \
            --FIELD_NAME 'N/A' \
            --FIELD_VALUE 'N/A' \
            --WORKFLOW 'Illumina Genomics Architecture - NovaSeq Sequencing v2.1' \
            --STEP 'AUTOMATED - NovaSeq Run (IGA v2.1)' \
            --INPUTS_OR_OUTPUTS 'OUTPUTS' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_completed.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/register_sample.groovy' && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:validate_flowcell_for_input_pools -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -validateSingleOutput true -poolType bulk"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2:http} -u {username} -p {password} script:evaluateDynamicExpression -exp 'if ( !output.container.name.matches( ::LP[0-9]{7}-BPP:: ) ) {fail ( ::Invalid BPP Plate Barcode. This plate ID must be in the format LPxxxxxxx-BPP, where 'x' is a digit 0-9, e.g. LP1234567-BPP. Please verify and try again.:: ) }' -log {compoundOutputFileLuid0} \
    && PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/validate_multiple_destination_plates.py -s {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'output.::Loading Workflow Type:: = input.::Loading Workflow Type::; output.::Flowcell Type:: = input.::Flowcell Type::' -log {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} -t true -log {compoundOutputFileLuid0} \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'step.::Number of Samples in Pool:: = step.::Number of Samples in Pool:: + 1' \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'if ( input.::Flowcell Type:: == ::SP:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Lanes to Sequence:: * 18+ 30 } ; if ( input.::Flowcell Type:: == ::S1:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Lanes to Sequence:: * 18+ 30 } ; if ( input.::Flowcell Type:: == ::S2:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Lanes to Sequence:: * 22 + 30 } ; if ( input.::Flowcell Type:: == ::S4:: ) { step.::Bulk Pool Volume (ul):: = step.::Number of Lanes to Sequence:: * 30 + 30 } ; input.::Per Sample Volume (ul):: = ( ( (input.::Final Loading Concentration (pM):: * 5 / 1000) / input.::Normalized Molarity (nM):: ) * step.::Bulk Pool Volume (ul):: ) / step.::Number of Samples in Pool::' \
        script:calculate_adjusted_per_sample_volume \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'step.::Total Sample Volume (ul):: = step.::Total Sample Volume (ul):: + input.::Adjusted Per Sample Volume (ul)::' \
        script:evaluateDynamicExpression \
            -h false \
            -exp 'if (step.::Total Sample Volume (ul):: >= step.::Bulk Pool Volume (ul)::) {output.::RSB Volume (ul):: = 0} else {output.::RSB Volume (ul):: = step.::Bulk Pool Volume (ul):: - step.::Total Sample Volume (ul)::} ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type::' \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} -t true -log {compoundOutputFileLuid0} \
    script:evaluateDynamicExpression \
    -h false \
    -exp 'step.::Number of Samples in Pool:: = step.::Number of Samples in Pool:: - 1; step.::Total Sample Volume (ul):: = step.::Total Sample Volume (ul):: - input.::Adjusted Per Sample Volume (ul)::' \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
    script:driver_file_generator \
    -i {stepURI:v2} \
    -u {username} \
    -p {password} \
    -q true \
    -destLIMSID {compoundOutputFileLuid1} \
    -t /opt/gls/clarity/extensions/IGA_2.1/hamilton_fast_prep/templatefiles/MakeBPFile_NovaSeq_template.csv \
    -o Output_plate_name.csv \
    -l {compoundOutputFileLuid2} && \
    PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 \
    /opt/gls/clarity/extensions/IGA_2.1/make_bpp/apply_multiple_bulk_pools.py \
    -s {stepURI:v2} \
    -u {username} \
    -p {password} \
    --min-volume {udf:Minimum Per Sample Volume (ul)} \
    --selected-cf {udf:Apply Correction Factors} \
    --hamilton-limsid {compoundOutputFileLuid1} \
    --custom-cf-limsid {compoundOutputFileLuid3} \
    -l {compoundOutputFileLuid4} "
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'output.::Flowcell Type:: = input.::Flowcell Type:: ; nextStep = ::ADVANCE::' -log {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_completed.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/pooling.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:validateUniqueIndexes"
    bash -l -c "/usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/03_NovaSeqXp_consolidateBulkPoolFiles.py \
    -u {username} -p {password} -s {stepURI} -o consolidated.csv --destLIMSID  {compoundOutputFileLuid2} && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:validate_flowcell_for_input_pools -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "/usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/03_NovaSeqXp_confirmBPPPlateAndStoreInstrumentID.py -u {username} -p {password} -s {stepURI} -f {compoundOutputFileLuid3} -i 'Liquid Handling Instrument ID'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2:http} -u {username} -p {password} script:evaluateDynamicExpression -exp 'if ( !output.container.name.matches( ::LP[0-9]{7}-WPP:: ) ) {fail ( ::Invalid WPP Plate Barcode. This plate ID must be in the format LPxxxxxxx-WPP, where 'x' is a digit 0-9, e.g. LP1234567-WPP. Please verify and try again.:: ) }' -log {compoundOutputFileLuid1} && /usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/hamilton_fast_prep/01_A_CFP_Batching_defaultContainerCheck.py -u {username} -p {password} -s {stepURI}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} \
        script:evaluateDynamicExpression \
            -t true \
            -h false \
            -exp 'if ( input.::Flowcell Type:: == ::SP:: ) { output.::BP Aliquot Volume (ul):: = 18 ; output.::NaOH Volume (ul):: = 4.50 ; output.::Tris-HCl Volume (ul):: = 4.50 ; step.::DPX1 Volume (ul):: = 126 ; step.::DPX2 Volume (ul):: = 18 ; step.::DPX3 Volume (ul):: = 66 ; output.::Mastermix per Lane (ul):: = 63} ; if ( input.::Flowcell Type:: == ::S1:: ) { output.::BP Aliquot Volume (ul):: = 18 ; output.::NaOH Volume (ul):: = 4.50 ; output.::Tris-HCl Volume (ul):: = 4.50 ; step.::DPX1 Volume (ul):: = 126 ; step.::DPX2 Volume (ul):: = 18 ; step.::DPX3 Volume (ul):: = 66 ; output.::Mastermix per Lane (ul):: = 63} ; if ( input.::Flowcell Type:: == ::S2:: ) { output.::BP Aliquot Volume (ul):: = 22 ; output.::NaOH Volume (ul):: = 5.50 ; output.::Tris-HCl Volume (ul):: = 5.50 ; step.::DPX1 Volume (ul):: = 126 ; step.::DPX2 Volume (ul):: = 18 ; step.::DPX3 Volume (ul):: = 66 ; output.::Mastermix per Lane (ul):: = 77} ; if ( input.::Flowcell Type:: == ::S4:: ) { output.::BP Aliquot Volume (ul):: = 30 ; output.::NaOH Volume (ul):: = 7.50 ; output.::Tris-HCl Volume (ul):: = 7.50 ; step.::DPX1 Volume (ul):: = 315 ; step.::DPX2 Volume (ul):: = 45 ; step.::DPX3 Volume (ul):: = 165 ; output.::Mastermix per Lane (ul):: = 105} ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type::' \
            -log {compoundOutputFileLuid1} \
    && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} \
        script:driver_file_generator \
            -t /opt/gls/clarity/extensions/conf/driverfiletemplates/NovaSeq_Xp_Working_Pool.csv \
            -o {compoundOutputFileLuid0}.csv \
        script:driver_file_generator \
            -t /opt/gls/clarity/extensions/conf/driverfiletemplates/NovaSeq_Xp_Working_Pool2.csv \
            -o append.csv \
    && cat append.csv >> {compoundOutputFileLuid0}.csv \
    && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
    script:driver_file_generator \
    -i {stepURI:v2} \
    -u {username} \
    -p {password} \
    -q true \
    -destLIMSID {compoundOutputFileLuid4} \
    -t /opt/gls/clarity/extensions/IGA_2.1/hamilton_fast_prep/templatefiles/LoadToFlowcell_NovaSeqXp_Incomplete_template.csv \
    -o Output_plate_name.csv \
    -l {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'output.::Flowcell Type:: = input.::Flowcell Type:: ; nextStep = ::ADVANCE::' -log {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_completed.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -t false -h false -exp 'output.::Flowcell Type:: = input.::Flowcell Type:: ; nextStep = ::ADVANCE::' -log {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:validate_flowcell_for_input_pools -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -validateSelectedContainer true && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_started.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} \
        script:evaluateDynamicExpression \
            -exp 'if (input.::Flowcell Type:: == ::SP:: && !output.container.name.matches( ::[A-Z0-9]{5}DR[A-Z0-9]{2}:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S1:: && !output.container.name.matches( ::[A-Z0-9]{5}DR[A-Z0-9]{2}:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S2:: && !output.container.name.matches( ::[A-Z0-9]{5}DM[A-Z0-9]{2}:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S4:: && !output.container.name.matches( ::[A-Z0-9]{5}DS[A-Z0-9]{2}:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type::' \
            -log {compoundOutputFileLuid1} && \
    /usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/validate_floorcell_container.py -u {username} -p {password} -s {stepURI}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} \
        script:evaluateDynamicExpression \
            -exp 'step.::Run Mode:: = input.::Flowcell Type:: ; if (!step.::Experiment Name::.matches(::[a-zA-Z0-9-_]+::)) { fail(::Experiment Name contains prohibited characters. Allowed characters are: a-z, A-Z, 0-9, -, and _::) }; if (step.::Workflow Type:: == ::No Index::) { if (step.::Index Read 1:: != 0) { fail(::Index Read 1 must be 0 if the Workflow Type is No Index.::) } } else { if (step.::Index Read 1:: == 0) { fail(::Index Read 1 must be greater than 0 if the Workflow Type is :: + step.::Workflow Type:: + ::.::) } }; if (step.::Paired End::.toBoolean() && step.::Read 2 Cycles:: == 0) { fail(::Read 2 Cycles must not be zero if it is Paired End read.::) }; if (step.::Workflow Type:: == ::Dual Index:: && step.::Index Read 2:: == 0) { fail(::Index Read 2 must not be zero if Workflow Type is Dual Index.::) }; if (step.::Workflow Type:: == ::No Index:: || step.::Workflow Type:: == ::Single Index::) { step.::Index Read 2:: = 0 }; if (!step.::Paired End::.toBoolean()) { step.::Read 2 Cycles:: = 0 }; if (input.::Flowcell Type::!=::SP:: && step.::Read 1 Cycles:: > 151) { fail(::Read 1 Cycles must not be larger than 151 if it is not SPrime Flowcell::) };if (input.::Flowcell Type::!=::SP:: && step.::Read 2 Cycles:: > 151) { fail(::Read 2 Cycles must not be larger than 151 if it is not SPrime Flowcell::) }; nextStep = ::ADVANCE::' \
            -log {compoundOutputFileLuid1} \
            -t true \
    && if [[ '{udf:SampleSheet Version}' == 'V2' && '{udf:Enable Secondary Analysis}' == 'false' ]]; then \
    templateFilename='/opt/gls/clarity/extensions/IGA_2.1/ss_converter_templates/NovaSeq_BCL2FASTQ_Samplesheet_XP_V2.csv'; \
           else \
    templateFilename='/opt/gls/clarity/extensions/IGA_2.1/ss_converter_templates/NovaSeq_BCL2FASTQ_Samplesheet_XP_V1.csv'; \
    fi \
    && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar -i {stepURI:v2} -u {username} -p {password} \
        script:driver_file_generator \
            -t $templateFilename \
            -o {compoundOutputFileLuid0}.csv \
            -q true \
            -destLIMSID {compoundOutputFileLuid0} \
            -l {compoundOutputFileLuid1} \
    && if [[ '{udf:Enable Secondary Analysis}' == 'true' ]]; then \
    PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 /opt/gls/clarity/extensions/IGA_2.1/ss_converter \
            --input {compoundOutputFileLuid0}.csv  \
            --bssh-app {udf:BaseSpace App Slug} \
            --stepURI {stepURI:v2} -u {username} -p {password} -q \
            --destLIMSID {compoundOutputFileLuid0} 2>&1; \
    fi && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar \
      -i {stepURI:v2} -u {username} -p {password} \
      script:driver_file_generator \
            -t /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/Biosample_Manifest.csv \
            -o {compoundOutputFileLuid3}.csv \
            -q true \
            -destLIMSID {compoundOutputFileLuid3} \
            -l {compoundOutputFileLuid1}"
    bash -l -c "/usr/bin/env python /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/04_NovaSeqXp_completeAndConsolidateWPPZipFile.py -u {username} -p {password} -s {stepURI} -o wpp_output --destLIMSID {compoundOutputFileLuid2}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid1} -s 'com/illumina/upa/scripts/common/step_completed.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} \
        script:evaluateDynamicExpression \
            -exp 'if (input.::Flowcell Type:: == ::SP:: && !output.container.name.matches( ::[A-Za-z0-9]{5}DRXX:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S1:: && !output.container.name.matches( ::[A-Za-z0-9]{5}DRXX:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S2:: && !output.container.name.matches( ::[A-Za-z0-9]{5}DMXX:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; if (input.::Flowcell Type:: == ::S4:: && !output.container.name.matches( ::[A-Za-z0-9]{5}DSXX:: ) ) {fail ( ::Invalid Flowcell Barcode. Please verify and try again.:: ) } ; output.::Flowcell Type:: = input.::Flowcell Type:: ; output.::Loading Workflow Type:: = input.::Loading Workflow Type::' \
            -log {compoundOutputFileLuid1}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_completed.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/novaseq6000/automated_sequencing_run_step_completed.groovy'"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {stepURI:v2} -u {username} -p {password} script:evaluateDynamicExpression -exp 'nextStep = ::ADVANCE::' -log {compoundOutputFileLuid0}"
    bash -l -c "PYTHONPATH=/opt/gls/clarity/extensions/IGA_2.1 python3 \
    /opt/gls/clarity/extensions/IGA_2.1/iga_novaseq/NovaSeq_automated_warning.py \
    -s {stepURI:v2} \
    -u {username} \
    -p {password} \
    -l {compoundOutputFileLuid0} && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/register_sample.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/common/step_started.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/novaseq6000/register_novaseq_run.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/novaseq6000/novaseq_associate_seqrun.groovy' && \
    /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/unified-product-analytics/automation/unified-product-analytics-automation.jar script:executeUPAAutomationScript -i {stepURI:v2} -u {username} -p {password} -l {compoundOutputFileLuid0} -s 'com/illumina/upa/scripts/novaseq6000/novaseq_seqrun_started.groovy' "

    Container

    Container Name

    Built-in

    Container

    Intensity Cycle 1 R1

    Numeric

    Read Only

    Container

    Intensity Cycle 1 R2

    Numeric

    Read Only

    Container

    LIMS ID (Container)

    Built-in

    Container

    Read PF (M) R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    Read PF (M) R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    Well

    Built-in

    Container

    Yield PF (Gb) R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    Yield PF (Gb) R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Aligned R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Aligned R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Bases >=Q30 R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Bases >=Q30 R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Error Rate R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Error Rate R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    %PF R1

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    %PF R2

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Container

    % Phasing R1

    Numeric

    Read Only

    Decimal Places Displayed = 3

    Container

    % Phasing R2

    Numeric

    Read Only

    Decimal Places Displayed = 3

    Container

    % Prephasing R1

    Numeric

    Read Only

    Decimal Places Displayed = 3

    Container

    % Prephasing R2

    Numeric

    Read Only

    Decimal Places Displayed = 3

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Default = None

    Default = Run Monitoring And Storage

    0

  • Default = 10

  • Range From 0 to 20

  • Decimal Places Displayed = 0

  • 0

  • Default = 10

  • Range From 0 to 20

  • Decimal Places Displayed = 0

  • 51

  • Default = 151

  • Range From 1 to 301

  • Decimal Places Displayed = 0

  • 51

  • Default = 151

  • Range From 0 to 301

  • Decimal Places Displayed = 0

  • SP

  • Default = S4

  • Custom

  • Default = Dual Index

  • Default = None

    Default = Run Monitoring And Storage

    0

  • Default = 10

  • Range From 0 to 20

  • Decimal Places Displayed = 0

  • 0

  • Default = 10

  • Range From 0 to 20

  • Decimal Places Displayed = 0

  • 51

  • Default = 151

  • Range From 1 to 301

  • Decimal Places Displayed = 0

  • 51

  • Default = 151

  • Range From 0 to 301

  • Decimal Places Displayed = 0

  • Custom

  • Default = Dual Index

  • Derived Sample

    Reagent Name

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Reagent Name

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Adjusted Per Sample Volume (ul)

    Numeric

    • Read Only

    • Decimal Places Displayed = 2

    Derived Sample

    Final Loading Concentration (pM)

    Numeric Dropdown

    • Required Field

    • Custom Entries

    • Presets

      • 225

      • 400

    • Decimal Places Displayed = 0

    Derived Sample

    Flowcell Type

    Text Dropdown

    • Required Field

    • Presets

      • SP

      • S1

      • S2

      • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    • Required Field

    • Presets

      • NovaSeq Standard

      • NovaSeq Xp

      • [Remove from workflow]

    Derived Sample

    Minimum Molarity (nM)

    Numeric

    • Decimal Places Displayed = 2

    Derived Sample

    Normalized Molarity (nM)

    Numeric

    • Decimal Places Displayed = 2

    Derived Sample

    Per Sample Volume (ul)

    Numeric

    • Read Only

    • Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Warning

    Text

    • Read Only

    Project

    Project Name

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Normalized Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Normalized Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    NaOH Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Derived Sample

    RSB Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Tris-HCl Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Derived Sample

    Volume of Pool to Denature (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 0

    Project

    Project Name

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Normalized Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Normalized Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    RSB Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    BP Aliquot Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 0

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Mastermix per Lane (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 0

    Derived Sample

    NaOH Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Tris-HCl Volume (ul)

    Numeric

    Read Only

    Decimal Places Displayed = 2

    Project

    Project Name

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Flowcell Type

    Text Dropdown

    Required Field

    Presets

    • SP

    • S1

    • S2

    • S4

    Derived Sample

    Loading Workflow Type

    Text Dropdown

    Required Field

    Presets

    • NovaSeq Standard

    • NovaSeq Xp

    • [Remove from workflow]

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Built-in

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Cluster Density (K/mm^2) R1

    Numeric

    Read Only

    Container

    Cluster Density (K/mm^2) R2

    Numeric

    Read Only

    IGA Library Prep Automated v2.1

    hashtag
    Overview

    IGA Library Prep Automated v2.1 contains preset protocols that support the preparation of samples and libraries used for sequencing. These protocols can be used with the IGA NovaSeq Sequencing v2.1 workflow and NextSeq 1000/2000 v2.3 workflow (which is installed separately). The protocols provide the following functions:

    • File-based integration with the Hamilton robots that are used for liquid handling steps.

    • Automated calculation of sample and buffer volumes.

    • Automated calculation or display of reagents.

    • When required, automatic step transition.

    hashtag
    Protocol 1: Sample Selection

    Protocol Type = Sample Prep

    Next Steps Configuration

    hashtag
    Step 1: Select Samples

    • Master Step Name = Select Samples (IGA v2.1)

    • Step Type = No Outputs

    hashtag
    Automations

    chevron-rightValidate Sample Attributes (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon entry

    chevron-rightSample Selection - Set Library prep method and Next steps (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon exit

    chevron-rightSample Selection - Route plated gDNA (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon exit

    hashtag
    Queue

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Row

    • Sample Table

    hashtag
    Ice Bucket

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Row

    • Sample Table (Column Headers)

    hashtag
    Record Details

    • Step Data (Master Step Fields)

    hashtag
    Protocol 2: Sample Plating

    Protocol Type = Sample Prep

    Next Steps Configuration

    hashtag
    Step 1: Plate Samples

    • Master Step Name = Sample Plating (IGA v2.1)

    • Step Type = Standard

    • Derived Sample Generation = Variable

    • Naming Convention = {InputItemlName}

    hashtag
    Automations

    chevron-rightSample Plating & Extraction - Validate Single Sample Type and Library Prep Method (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon entry

    chevron-rightPlacement Reminder (IGA v2.1)hashtag
    • Trigger Location = Placement

    • Trigger Style = Automatic upon entry

    chevron-rightSample Plating - Sample Placement SAM Plate Barcode Uniqueness Check (IGA v2.1)hashtag
    • Trigger Location = Placement

    • Trigger Style = Automatic upon exit

    chevron-rightSample Plating - Set Transfer Volume & Create Liquid Handler Input File (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Manual button

    chevron-rightSample Plating - Hamilton Output Plate Barcode Check, Store Instrument ID & Set Next Steps to Remove from Workflow before Custom Routing (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon exit

    chevron-rightSample Plating - Route samples (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon exit

    hashtag
    Queue

    • Defaults

      • Sample Grouping = Group by Projects

      • Well Sort Order = Column

    • Sample Table

    hashtag
    Ice Bucket

    • Defaults

      • Sample Grouping = Group by Projects

      • Well Sort Order = Column

    • Sample Table (Column Headers)

    hashtag
    Placement = Enabled

    • Defaults

      • Sample Grouping = Group by Projects

      • Well Sort Order = Column

      • Placement Pattern = Column

    hashtag
    Record Details

    • Step Data (Master Step Fields)

    hashtag
    Protocol 3: Blood Extraction

    Protocol Type = Sample Prep

    Next Steps Configuration

    hashtag
    Step 1: DNA Extraction - Blood

    • Master Step Name = DNA Extraction - Blood (IGA v2.1)

    • Step Type = Standard

    • Derived Sample Generation = Fixed, 1

    • Naming Convention = {InputItemName}

    hashtag
    Automations

    chevron-rightSample Plating & Extraction - Validate Single Sample Type and Library Prep Method (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon entry

    chevron-rightExtraction - Sample Placement EDP Plate Barcode Uniqueness Check (IGA v2.1)hashtag
    • Trigger Location = Placement

    • Trigger Style = Automatic upon exit

    chevron-rightExtraction - Count Samples & Create LH Input File (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon entry

    chevron-rightExtraction - Check LH Output File Barcode & Parse Reagent Info & Check for Missing Barcodes & Set Next Steps to Remove from Workflow (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon exit

    chevron-rightExtraction - Routing (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon exit

    hashtag
    Queue

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

    • Sample Table (Column Headers)

    hashtag
    Ice Bucket

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

    • Sample Table (Column Headers)

    hashtag
    Placement = Enabled

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

      • Placement Pattern = Column

    hashtag
    Record Details

    • Step Data (Master Step Fields)

    hashtag
    Protocol 4: Saliva Extraction

    Protocol Type = Sample Prep

    Next Steps Configuration

    hashtag
    Step 1: DNA Extraction - Saliva

    • Master Step Name = DNA Extraction - Blood (IGA v2.1)

    • Step Type = Standard

    • Derived Sample Generation = Fixed, 1

    • Naming Convention = {InputItemName}

    hashtag
    Automations

    chevron-rightSample Plating & Extraction - Validate Single Sample Type and Library Prep Method (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon entry

    chevron-rightExtraction - Sample Placement EDP Plate Barcode Uniqueness Check (IGA v2.1)hashtag
    • Trigger Location = Placement

    • Trigger Style = Automatic upon exit

    chevron-rightExtraction - Count Samples & Create LH Input File (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon entry

    chevron-rightExtraction - Check LH Output File Barcode & Parse Reagent Info & Check for Missing Barcodes & Set Next Steps to Remove from Workflow (IGA v2.1)hashtag
    • Trigger Location = Record Details

    • Trigger Style = Automatic upon exit

    chevron-rightExtraction - Routing (IGA v2.1)hashtag
    • Trigger Location = Step

    • Trigger Style = Automatic upon exit

    hashtag
    Queue

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

    • Sample Table (Column Headers)

    hashtag
    Ice Bucket

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

    • Sample Table (Column Headers)

    hashtag
    Placement = Enabled

    • Defaults

      • Sample Grouping = Group by Containers

      • Well Sort Order = Column

      • Placement Pattern = Column

    hashtag
    Record Details

    • Step Data (Master Step Fields)

    hashtag
    Protocol 5: Illumina DNA PCR-Free

    Protocol Type = Sample Prep

    Ne