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Clarity LIMS Software
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Clarity LIMS Software
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  • Clarity LIMS
    • Clarity & LabLink
  • API and Database
    • API Portal
      • REST
        • REST General Concepts
        • REST Web Services
        • HTTP Response Codes and Errors
        • XML UTF-8 Character Encoding
        • Requesting API Version Information
        • Viewing Paginated List Resources
        • Filtering List Resources
        • Working with User-Defined Fields (UDF) and Types (UDT)
        • Traversing a Genealogy
        • Working with Batch Resources
      • Getting Started with API
        • Understanding API Terminology (LIMS v5 and later)
        • API-Based URIs (LIMS v4 and later)
        • Development Prerequisites
        • Structure of REST Resources
        • The Life Cycle of a Sample: Stages Versus Steps
        • Integrating Scripts
      • Automation
        • Automation Triggers and Command Line Calls
        • Automation Execution Environment
        • Supported Command Line Interpreters
        • Automation Channels
        • Error Handling
        • Automation Tokens
          • Derived Sample Automation Tokens
          • Step Automation Tokens
          • Project Automation Tokens
        • Automation Testing
        • Troubleshooting Automation
      • Tips and Tricks
        • Accessing Step UDFs from a different Step
        • Obfuscating Sensitive Data in Scripts
        • Integrating Clarity LIMS with Upstream Sample Accessioning Systems
        • Creating Samples and Projects via the API
        • Displaying Files From an Earlier Step
        • Transitioning Output Artifacts into the Next Step
        • Determining the Workflow(s) to Which a Sample is Assigned
        • Standardizing Sample Naming via the API
        • Copying UDF Values from Source to Destination
        • Updating Preset Value of a Step UDF through API
        • Automating BCL Conversion
        • Finding QC Flags in Aggregate QC (Library Validation) via REST API
        • Setting the Value of a QC Flag on an Artifact
        • Creating Notifications When Files are Added via LabLink
        • Remote HTTP Filestore Setup
      • Cookbook
        • Get Started with the Cookbook
          • Tips and Troubleshooting
          • Obtain and Use the REST API Utility Classes
        • Work with EPP/Automation and Files
          • Automation Trigger Configuration
          • Process Execution with EPP/Automation Support
        • Work with Submitted Samples
          • Adding Samples to the System
          • Renaming Samples
          • Assigning Samples to Workflows
          • Updating Sample Information
          • Show the Relationship Between Samples and Analyte Artifacts (Derived Samples)
        • Work with Containers
          • Add an Empty Container to the System
          • Find the Contents of a Well Location in a Container
          • Filter Containers by Name
        • Work with Derived Sample Automations
          • Remove Samples from Workflows
          • Requeue Samples
          • Rearray Samples
        • Work with Process/Step Outputs
          • Update UDF/Custom Field Values for a Derived Sample Output
          • Rename Derived Samples Using the API
          • Find the Container Location of a Derived Sample
          • Traverse a Pooled and Demultiplexed Sample History/Genealogy
          • View the Inputs and Outputs of a Process/Step
        • Work with Projects and Accounts
          • Remove Information from a Project
          • Add a New Project to the System with UDF/Custom Field Value
          • Get a Project Name
          • Find an Account Registered in the System
          • Update Contact (User and Client) Information
        • Work with Multiplexing
          • Find the Index Sequence for a Reagent Label
          • Demultiplexing
          • Pool Samples with Reagent Labels
          • Apply Reagent Labels with REST
          • Apply Reagent Labels When Samples are Imported
          • Apply Reagent Labels by Adding Reagents to Samples
        • Working with User Defined Fields/Custom Fields
          • About UDFs/Custom Fields and UDTs
          • Performing Post-Step Calculations with Custom Fields/UDFs
        • Work with Processes/Steps
          • Filter Processes by Date and Type
          • Find Terminal Processes/Steps
          • Run a Process/Step
          • Update UDF/Custom Field Information for a Process/Step
          • Work with the Steps Pooling Endpoint
        • Work with Batch Resources
          • Introduction to Batch Resources
          • Update UDF/Custom Field Information with Batch Operations
          • Retrieve Multiple Entities with a Single API Interaction
          • Select the Optimal Batch Size
        • Work with Files
          • Attach a File with REST and Python
          • Attach Files Located Outside the Default File Storage Repository
          • Attach a File to a File Placeholder with REST
        • Work with Controls
          • Automated Removal of Controls from a Workflow
      • Application Examples
        • Python API Library (glsapiutil.py) Location
        • Scripts That Help Automate Steps
          • Route Artifacts Based Off a Template File
          • Invoking bcl2fastq from BCL Conversion and Demultiplexing Step
          • Email Notifications
          • Finishing the Current Step and Starting the Next
          • Adding Downstream Samples to Additional Workflows
          • Advancing/Completing a Protocol Step via the API
          • Setting a Default Next Action
          • Automatic Placement of Samples Based on Input Plate Map (Multiple Plates)
          • Automatic Placement of Samples Based on Input Plate Map
          • Publishing Files to LabLink
          • Automatic Pooling Based on a Sample UDF/Custom Field
          • Completing a Step Programmatically
          • Automatic Sample Placement into Existing Containers
          • Routing Output Artifacts to Specific Workflows/Stages
          • Creating Multiple Containers / Types for Placement
          • Starting a Protocol Step via the API
          • Setting Quality Control Flags
          • Applying Indexing Patterns to Containers Automatically
          • Assignment of Sample Next Steps Based On a UDF
          • Parsing Metadata into UDFs (BCL Conversion and Demultiplexing)
        • Scripts That Validate Step Contents
          • Validating Process/Step Level UDFs
          • Checking That Containers Are Named Appropriately
          • Checking for Index Clashes Based on Index Sequence
          • Validating Illumina TruSeq Index Adapter Combinations
        • Scripts Triggered Outside of Workflows/Steps
          • Repurposing a Process to Upload Indexes
          • Adding Users in Bulk
          • Moving Reagent Kits & Lots to New Clarity LIMS Server
          • Programatically Importing the Sample Submission Excel File
          • Generating an MS Excel Sample Submission Spreadsheet
          • Assigning Samples to New Workflows
        • Miscellaneous Scripts
          • Illumina LIMS Integration
          • Generating a Hierarchical Sample History
          • Protocol-based Permissions
          • Self-Incremental Counters
          • Generic CSV Parser Template (Python)
          • Renaming Samples to Add an Internal ID
          • Creating Custom Sample Sheets
          • Copying Output UDFs to Submitted Samples
          • Parsing Sequencing Meta-Data into Clarity LIMS
          • Submit to a Compute Cluster via PBS
          • Downloading a File and PDF Image Extraction
        • Resources and References
          • Understanding LIMS ID Prefixes
          • Container States
          • Useful Tools
          • Unsupported Artifact Types
          • Unsupported Process Types
          • Suggested Reading
          • API Training Videos
  • Illumina Preset Protocols
    • IPP v2.10
      • Release Notes
      • Installation and User Configuration
      • Manual Upgrade
    • IPP v2.9
      • Release Notes
      • Installation and User Configuration
    • IPP v2.8
      • Release Notes
      • Installation and User Configuration
      • Manual Upgrade
    • IPP v2.7
      • Release Notes
      • Installation and User Configuration
    • IPP v2.6
      • Release Notes
      • Installation and User Configuration
      • Manual Upgrade
  • Sample Prep
    • QC and Sample Prep
      • DNA Initial QC 5.1.2
      • RNA Initial QC 5.1.2
      • Library Validation QC 5.1.2
  • Library Prep
    • AmpliSeq for Illumina
      • BRCA Panel
        • Library Preparation v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Cancer HotSpot Panel v2
        • Library Preparation v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Childhood Cancer Panel
        • DNA Library Prep v1.1
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Comprehensive Cancer Panel
        • Library Preparation v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Comprehensive Panel v3
        • DNA Library Prep v1.1
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Custom DNA Panel
        • Library Preparation v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Focus Panel
        • DNA Library Prep v1.1
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Immune Repertoire Panel
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Immune Response Panel
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • Myeloid Panel
        • DNA Library Prep v1.1
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
      • TCR beta-SR Panel
        • DNA Library Prep v1.1
        • RNA Library Prep v1.1
      • Transcriptome Human Gene Expression Panel
        • RNA Library Prep v1.1
        • Equalizer v1.1
        • Standard v1.1
    • Library Prep Validation
    • Nextera
      • Nextera Mate Pair v1.0
      • Nextera Rapid Capture Custom Enrichment v2.0
      • Nextera XT v2.0
    • Targeted Enrichment
      • Illumina DNA Prep with Enrichment (S) Tagmentation v1.2
      • Illumina RNA Prep with Enrichment (L) Tagmentation v1.1
    • TruSeq
      • TruSeq ChIP-Seq v1.0
      • TruSeq Custom Amplicon v1.0
      • TruSeq DNA Exome v2.0
      • TruSeq DNA PCR-Free v2.0
      • TruSeq Methyl Capture EPIC v2.0
      • TruSeq Nano DNA v1.0
      • TruSeq RNA Access v2.0
      • TruSeq RNA Exome v1.0
      • TruSeq Small RNA v1.0
      • TruSeq Stranded mRNA v2.0
    • TruSight
      • TruSight Oncology 500 ctDNA v1.1
      • TruSight Oncology 500 HT v1.1
      • TruSight Oncology 500 v1.1
      • TruSight Tumor 170 v2.0
    • Other DNA Protocols
      • Illumina DNA PCR-Free Library Prep Manual v1.1
      • Illumina DNA Prep (M) Tagmentation v1.0
    • Other RNA Protocols
      • Illumina Stranded mRNA Prep Ligation 1.1
      • Illumina Stranded Total RNA Prep Ligation with Ribo-Zero Plus v1.1
  • iLASS & Infinium Arrays
    • iLASS
      • iLASS Infinium Genotyping v1.1
        • iLASS Infinium Batch DNA v1.1
        • iLASS Infinium Genotyping Assay v1.1
        • iLASS Infinium Genotyping with PGx Assay v1.1
      • iLASS Infinium Genotyping v1.0
        • iLASS Infinium Genotyping Assay v1.0
        • iLASS Infinium Genotyping with PGx Assay v1.0
    • Infinium Arrays
      • Infinium HD Methylation Assay Manual v1.2
      • Infinium HTS Assay Manual v1.2
      • Infinium LCG Assay Manual v1.2
      • Infinium XT Assay Manual v1.2
      • GenomeStudio v1.0
  • Applications
    • IGA
      • IGA v2.1
        • IGA Library Prep Automated v2.1
        • IGA NovaSeq Sequencing v2.1
    • Viral Pathogen Protocols
      • CDC COVID-19 RT-PCR
        • Sort Specimens to Extraction v1.1
        • Qiagen QIAamp DSP Viral RNA Mini Kit v1.1
        • Qiagen EZ1 Advanced XL v1.1
        • Roche MagNA Pure LC v1.1
        • Roche MagNA Pure Compact v1.1
        • Roche MagNA Pure 96 v1.1
        • bioMerieux NucliSENS easyMAG Instrument v1.1
        • bioMerieux EMAG Instrument v1.1
        • Real-Time RT-PCR Prep v1.1
      • Illumina COVIDSeq v1.6
      • Respiratory Virus Panel v1.0
  • Instruments & Integrations
    • Compatibility
    • Integration Properties
      • Integration Properties Details
    • Clarity LIMS Product Analytics
      • Supported Workflows
      • Workflow Customization
      • Clarity LIMS Product Analytics v1.4.0
        • Configuration
      • Clarity LIMS Product Analytics v1.3.1
        • Configuration
      • Clarity LIMS Product Analytics v1.3.0
        • Configuration
      • Clarity LIMS Product Analytics v1.2.0
        • Configuration
    • Illumina Run Manager
      • Illumina Run Manager v1.0.0
        • Installation and User Interaction
    • iScan
      • iScan System
      • iScan v1.2.0
        • Release Notes
        • BeadChip Accessioning, Imaging, and Analysis
      • iScan v1.1.0
        • Release Notes
        • BeadChip Accessioning, Imaging, and Analysis
      • iScan System v1.0
    • iSeq 100 Run Setup v1.0
    • MiniSeq v1.0
    • MiSeq
      • MiSeq v8.3.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • MiSeq v8.2.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Manual Upgrade
    • MiSeq i100 (On-Prem)
      • MiSeq i100 On-Prem v1.0.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • MiSeq i100 (Hosted)
      • MiSeq i100 v1.0.0
        • Release Notes
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • MiSeqDx
      • MiSeqDx Sample Sheet Generation (v1.11.0 and later)
      • MiSeqDx v1.11.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • MiSeqDx v1.10.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Sample Sheet Generation
        • Manual Upgrade
    • Next Generation Sequencing Package
      • Release Notes
        • NGS Extensions v5.25.0
        • NGS Extensions v5.24.0
        • NGS Extensions v5.23.0
      • Accession Kit Lots
      • Auto-Placement of Reagent Indexes
      • Compute Replicate Average
      • Copy UDFs
      • Initialize Artifact UDFs
      • Label Non-Labeled Outputs
      • Linear Regression Calculation
      • Normalization Buffer Volumes
      • Process Summary Report
      • Routing Script
      • Set UDF
      • Validate Complete Plate
      • Validate Sample Count
      • Validate Unique Indexes
    • NextSeq 500/550
      • NextSeq 500/550 v2.5.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Manual Upgrade
      • NextSeq 500/550 v2.4.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • NextSeq 500/550 v2.3.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NextSeq 1000/2000 (Hosted)
      • NextSeq 1000/2000 v2.5.1
        • Release Notes
      • NextSeq 1000/2000 v2.5.0
        • Release Notes
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Manual Upgrade
      • NextSeq 1000/2000 v2.4.0
        • Release Notes
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NextSeq 1000/2000 (On-Prem)
      • NextSeq 1000/2000 On-Prem v1.0.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NovaSeq 6000 (API-based)
      • NovaSeq 6000 API-based v3.7.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • NovaSeq 6000 API-based v3.6.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Manual Upgrade
    • NovaSeq 6000 (File-based)
      • NovaSeq 6000 File-based v2.6.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • NovaSeq 6000 File-based v2.5.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NovaSeq 6000Dx (API-based)
      • NovaSeq 6000Dx API-based v1.3.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
      • NovaSeq 6000Dx API-based v1.2.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NovaSeq X Series (Hosted)
      • NovaSeq X Series v1.3.0
        • Release Notes
        • Configuration
        • Manual Upgrade
      • NovaSeq X Series v1.2.1
        • Release Notes
      • NovaSeq X Series v1.2.0
        • Release Notes
        • Configuration
        • User Interaction, Validation and Troubleshooting
        • Manual Upgrade
      • NovaSeq X Series v1.1.0
        • Release Notes
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • NovaSeq X Series (On-Prem)
      • NovaSeq X Series On-Prem v1.0.0
        • Release Notes
        • Installation
        • Configuration
        • User Interaction, Validation and Troubleshooting
    • References
      • Configure Multiple Identical netPathPrefixSearch Values
      • Configure Support for Samples Having Duplicate Names with Different Indexes
      • Illumina Instrument Sample Sheets
      • Terminology
  • Integration Toolkits
    • Lab Instrument Toolkit
      • Template File Generator
        • Creating Template Files
        • Template File Contents
        • Template File Generator Troubleshooting
      • Add Blank Lines
      • Convert CSV to Excel
      • Parse CSV
      • Name Matching XML Parser
      • Sample Placement Helper
    • Lab Logic Toolkit
      • Working with Lab Logic Toolkit
        • Data Collection Entities
        • Failing a Script
        • Mapping Field Types
        • Non-UDF/Custom Field Properties
        • Setting QC Flags
        • Setting Next Actions
        • Specifying Custom Fields
        • Working with Submitted Samples
        • Working with Containers
      • Lab Logic Toolkit Script Examples
        • Comparing Stop/Start Dates and Times with LLTK
      • Lab Logic Toolkit FAQ
  • Known Issues
    • Integration
      • Sample Sheet Generation Issue and CLPA Issues When Samples Have Been Assigned QC Flag Prior to Entering Steps
  • Security Bulletin
    • Investigation of OpenSSH vulnerability with Clarity LIMS
  • Resources
    • Third Party Software Information
  • Others
    • Revision History
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  • Protocol 1: RNA Library Prep (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 1: Dilute RNA (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 2: Qubit (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 3: Dilute RNA (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 4: Reverse Transcribe (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 5: Amplify cDNA Targets (AmpliSeq for Illumina Focus Panel v1.1)
  • Step 6: Partially Digest Amplicons (AmpliSeq for Illumina Focus Panel v1.1)

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  1. Library Prep
  2. AmpliSeq for Illumina
  3. Focus Panel

RNA Library Prep v1.1

PreviousDNA Library Prep v1.1NextEqualizer v1.1

Last updated 4 months ago

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Protocol 1: RNA Library Prep (AmpliSeq for Illumina Focus Panel v1.1)

Protocol Type = Library Prep

Next Steps Configuration

Step 1: Dilute RNA (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Dilute RNA (AmpliSeq for Illumina v1.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

Automations

Copy Concentration and Set Sample Volume
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

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.::Concentration:: = input.::Concentration:: ; output.::Conc. Units:: = input.::Conc. Units:: ; output.::Sample Volume (uL):: = 5' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - RNA
  • Trigger Location = Record Details

  • Trigger Style = Manual button

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 'output.::Total Volume (uL):: = (output.::Concentration::/step.::Desired Concentration (ng/uL)::) * output.::Sample Volume (uL):: ; \
output.::Nuclease-free water (uL):: = output.::Total Volume (uL):: - output.::Sample Volume (uL):: ; \
output.::Input Amount (ng):: = step.::Desired Concentration (ng/uL):: * output.::Total Volume (uL):: ' \
        -log {compoundOutputFileLuid0}"
Copy Desired Concentration
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

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.::Desired Concentration (ng/uL):: = step.::Desired Concentration (ng/uL)::' \
-log {compoundOutputFileLuid0}"
Set Next Step - Advance
  • Trigger Location = Not Used

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 = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Record Details

Group of Defaults

Immune Repertoire Panel
  • Directions = If enough RNA is available, dilute to intermediate concentration ~20-1000 ng/uL.

TCR beta-SR Panel
  • Default = If enough RNA is available, dilute to intermediate concentration ~20-1000 ng/uL.

  • Step Data

    • Group of Defaults = Immune Repertoire Panel

    • Master Step Fields

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Desired Concentration (ng/uL)

      Numeric

      Range = 0 To 1000

      Directions

      Multiline Text

      Read Only

      Default = If enough RNA is available, dilute to intermediate concentration ~20-50 ng/uL.

  • Step File Placeholders

    • Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Derived Sample

      Concentration

      Numeric

      Required Field

      Decimal Places Displayed = 2

      Derived Sample

      Conc. Units

      Text

      Required Field

      Derived Sample

      Desired Concentration (ng/uL)

      Numeric

      Derived Sample

      Input Amount (ng)

      Numeric

      Decimal Places Displayed = 0

      Derived Sample

      Nuclease-free water (uL)

      Numeric

      Decimal Places Displayed = 2

      Derived Sample

      Sample Name

      Built-in

      Derived Sample

      Sample Volume (uL)

      Numeric

      Decimal Places Displayed = 2

      Derived Sample

      Total Volume (uL)

      Numeric

      Decimal Places Displayed = 2

Step 2: Qubit (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Qubit (AmpliSeq for Illumina v1.1)

  • Step Type = Standard QC

  • Measurement Generation = Fixed, 1

  • Naming Convention = {InputItemName}

Automations

Assign QC flags (Qubit QC)
  • Trigger Location = Record Details

  • Trigger Style = Manual button

bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar -i {processURI:v2} -u {username} -p {password} script:assignQC -log {compoundOutputFileLuid1} -qcResult {compoundOutputFileLuid2}"
Set Next Step and Copy Concentration
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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 = ::ADVANCE:: ; input.::Concentration:: = output.::Concentration:: ; input.::Conc. Units:: = output.::Conc. Units::' -log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Record Details

  • Step Data (Master Step Fields)

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Criteria 1 - Operator

    Text

    Default = >=

    Criteria 1 - Source Data Field

    Text

    Default = Concentration

    Criteria 1 - Threshold Value

    Numeric

    Criteria 2 - Operator

    Text

    Default = <=

    Criteria 2 - Source Data Field

    Text

    Default = Concentration

    Criteria 2 - Threshold Value

    Numeric

  • Step File Placeholders

    • Log - Automatically attached

    • QC Log File - Automatically attached

    • QC Result File - Automatically attached

    • Upload File - Manually uploaded

  • Sample Table

    • Enable QC Flags = Yes

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • File Column Options

      • File Column Display = Hide

      • File Attachment Method = Auto

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Derived Sample

      Concentration

      Numeric

      Required Field

      Decimal Places Displayed = 2

      Derived Sample

      Conc. Units

      Text

      Required Field

      Derived Sample

      Sample Name

      Built-in

      Measurement

      Concentration

      Numeric

      Decimal Places Displayed = 2

      Measurement

      Conc. Units

      Text

Step 3: Dilute RNA (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Dilute RNA (AmpliSeq for Illumina v1.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

Automations

Copy Concentration and Set Sample Volume
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

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.::Concentration:: = input.::Concentration:: ; output.::Conc. Units:: = input.::Conc. Units:: ; output.::Sample Volume (uL):: = 5' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - RNA
  • Trigger Location = Record Details

  • Trigger Style = Manual button

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 'output.::Total Volume (uL):: = (output.::Concentration::/step.::Desired Concentration (ng/uL)::) * output.::Sample Volume (uL):: ; \
output.::Nuclease-free water (uL):: = output.::Total Volume (uL):: - output.::Sample Volume (uL):: ; \
output.::Input Amount (ng):: = step.::Desired Concentration (ng/uL):: * output.::Total Volume (uL):: ' \
        -log {compoundOutputFileLuid0}"
Set Next Step - Advance
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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 = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"
Copy Desired Concentration
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

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.::Desired Concentration (ng/uL):: = step.::Desired Concentration (ng/uL)::' \
-log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Record Details

  • Step Data (Master Step Fields)

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Desired Concentration (ng/uL)

    Numeric

    Range = 0 To 1000

    Directions

    Multiline Text

    Read Only

    Default = If enough RNA is available, dilute to intermediate concentration ~20-50 ng/uL.

  • Step File Placeholders

    • Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Derived Sample

      Concentration

      Numeric

      Required Field

      Decimal Places Displayed = 2

      Derived Sample

      Conc. Units

      Text

      Required Field

      Derived Sample

      Input Amount (ng)

      Numeric

      Decimal Places Displayed = 0

      Derived Sample

      Nuclease-free water (uL)

      Numeric

      Decimal Places Displayed = 2

      Derived Sample

      Sample Name

      Built-in

      Derived Sample

      Sample Volume (uL)

      Numeric

      Decimal Places Displayed = 2

      Derived Sample

      Total Volume (uL)

      Numeric

      Decimal Places Displayed = 2

Step 4: Reverse Transcribe (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Reverse Transcribe RNA (AmpliSeq for Illumina v1.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

  • Reagent Kits

    • AmpliSeq cDNA Synthesis for Illumina

      • Supplier = Illumina

      • Catalog Number = 20022654

    • AmpliSeq Focus Panel for RNA

      • Supplier = Illumina

      • Catalog Number = 20019164

Automations

Copy Concentration, Total Volume and Input Amount
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

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.::Total Samples:: = step.::Total Samples:: + 1' \
-log {compoundOutputFileLuid0} && /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.::Concentration:: = input.::Concentration:: ; \
output.::Conc. Units:: = input.::Conc. Units:: ; \
output.::Total Volume (uL):: = input.::Total Volume (uL):: ; \
output.::Input Amount (ng):: = input.::Input Amount (ng):: ; \
step.::Desired Concentration (ng/uL):: = input.::Desired Concentration (ng/uL)::' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - Focus Panel
  • Trigger Location = Record Details

  • Trigger Style = Manual button

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 7) {step.::Nuclease-free water (uL):: = (7 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 2; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 1' \
-log {compoundOutputFileLuid0}"
Set Next Step - Advance
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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 = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"
Calculate Input Amount
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 7) {step.::Nuclease-free water (uL):: = (7 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 2 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 1' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - Immune Repertoire Panel
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 3.5) {step.::Nuclease-free water (uL):: = (3.5 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 1 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 0.5' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - Immune Response Panel
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 7.0) {step.::Nuclease-free water (uL):: = (7.0 - (step.::Prep Input Volume (uL):: + output.::AmpliSeq ERCC RNA Spike-in Volume (uL)::)) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 1 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 0.5 ; \
step.::AmpliSeq ERCC RNA Spike-in Mix (uL):: = step.::Total Samples:: * output.::AmpliSeq ERCC RNA Spike-in Volume (uL):: *1.1' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - Myeloid Panel
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 3.5) {step.::Nuclease-free water (uL):: = (3.5 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 1 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 0.5' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - TCRbeta-SR
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 7) {step.::Nuclease-free water (uL):: = (7 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 2 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 1' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount - Transcriptome Human Genome Expression Panel
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 3.5) {step.::Nuclease-free water (uL):: = (3.5 - (step.::Prep Input Volume (uL):: + output.::AmpliSeq ERCC RNA Spike-in Volume (uL)::)) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 1 ; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 0.5 ; \
step.::AmpliSeq ERCC RNA Spike-in Mix (uL):: = step.::Total Samples:: * output.::AmpliSeq ERCC RNA Spike-in Volume (uL):: *1.1' \
-log {compoundOutputFileLuid0}"
Calculate Input Amount- Custom RNA Panel
  • Trigger Location = Not Used

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 'step.::Prep Input Volume (uL):: = step.::Prep Input Amount (ng):: / step.::Desired Concentration (ng/uL):: ; \
if (step.::Prep Input Volume (uL):: < 7) {step.::Nuclease-free water (uL):: = (7 - step.::Prep Input Volume (uL)::) * step.::Total Samples::*1.1} else {step.::Nuclease-free water (uL):: = 0} ; \
step.::5X AmpliSeq cDNA Reaction Mix (uL):: = step.::Total Samples:: * 1.1 * 2; \
step.::10X AmpliSeq RT Enzyme Mix (uL):: = step.::Total Samples:: * 1.1 * 1' \
-log {compoundOutputFileLuid0}"
Copy Concentration, Total Volume and Input Amount - Myeloid
  • Trigger Location = Not Used

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.::Total Samples:: = step.::Total Samples:: + 1' \
-log {compoundOutputFileLuid0} && /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.::Concentration:: = input.::Desired Concentration (ng/uL):: ; \
output.::Conc. Units:: = input.::Conc. Units:: ; \
output.::Total Volume (uL):: = input.::Total Volume (uL):: ; \
output.::Input Amount (ng):: = input.::Input Amount (ng):: ; \
step.::Desired Concentration (ng/uL):: = input.::Desired Concentration (ng/uL)::' \
-log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

    • Placement Pattern = Row

  • Destination Containers

    • 96 well plate

Record Details

Group of Defaults

Childhood Cancer Panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 10

  • Recommended Prep Input (ng) = Each reaction requires 1-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

  • Thermal Cycler Program = RT

  • Total Samples = 0

Comprehensive Panel v3
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 20

  • Recommended Prep Input (ng) = Each reaction requires 1-100 ng of DNase-treated total RNA per pool. The recommended input is 10 ng RNA per pool.

  • Thermal Cycler Program = RT

  • Total Samples = 0

Focus Panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 10

  • Recommended Prep Input (ng) = Each reaction requires 1-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

  • Thermal Cycler Program = RT

Immune Repertoire Panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 1000

  • Recommended Prep Input (ng) = Each reaction requires 10-1000 ng of DNase-treated total RNA. If RNA is not limiting, the recommended input is 1000 ng RNA. High RNA input amounts are recommended for rare clones.

  • Thermal Cycler Program = RT

Immune Response Panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 10

  • Recommended Prep Input (ng) = Each reaction requires 1-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

  • Thermal Cycler Program = RT

  • Total Samples = 0

Myeloid Panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 10

  • Recommended Prep Input (ng) = Each reaction requires 10-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

  • Thermal Cycler Program = RT

  • Total Samples = 0

TCR beta-SR panel
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 1000

  • Recommended Prep Input (ng) = Each reaction requires 50-1000 ng of DNase-treated total RNA. If RNA is not limited, the recommended input is 1000 ng RNA

  • Thermal Cycler Program = RT

Transcriptome HGx
  • AmpliSeq ERCC RNA Spike-in Mix = No

  • Directions = If RNA was prepared from FFPE tissue and never heat-treated, heat at 80°C for 10 minutes and then cool to room temperature before proceeding to reverse transcription.

  • Prep Input Amount (ng) = 10

  • Recommended Prep Input (ng) = Each reaction requires 1-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

  • Thermal Cycler Program = RT

  • Total Samples = 0

  • Step Data

    • Group of Defaults = Focus Panel

    • Master Step Fields

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      5X AmpliSeq cDNA Reaction Mix (uL)

      Numeric

      • Decimal Places Displayed = 1

      10X AmpliSeq RT Enzyme Mix (uL)

      Numeric

      • Decimal Places Displayed = 1

      Desired Concentration (ng/uL)

      Numeric

      Read Only

      Nuclease-free water (uL)

      Numeric

      • Decimal Places Displayed = 1

      Prep Input Amount (ng)

      Numeric

      • Default = 2

      • Range = 2 To 1000

      Prep Input Volume (uL)

      Numeric

      • Decimal Places Displayed = 2

      Recommended Prep Input (ng)

      Multiline Text

      Read Only

      • Default = Each reaction requires 1-100 ng of DNase-treated total RNA. The recommended input is 10 ng RNA.

      Thermal Cycler Program

      Text

      Read Only

      • Default = RT

      Total Samples

      Numeric

      • Default = 0

      • Decimal Places Displayed = 0

  • Step File Placeholders

    • Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Derived Sample

      Concentration

      Numeric

      Required Field

      Decimal Places Displayed = 2

      Derived Sample

      Conc. Units

      Text

      Required Field

      Derived Sample

      Input Amount (ng)

      Numeric

      Decimal Places Displayed = 0

      Derived Sample

      Sample Name

      Built-in

      Derived Sample

      Total Volume (uL)

      Numeric

      Decimal Places Displayed = 2

Step 5: Amplify cDNA Targets (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Amplify cDNA Targets (AmpliSeq for Illumina Focus Panel v1.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

  • Reagent Kits

    • AmpliSeq Focus Panel for RNA

      • Supplier = Illumina

      • Catalog Number = 20019164

    • AmpliSeq Library PLUS for Illumina

      • Supplier = Illumina

      • Catalog Number = 24 - 20019101; 96 - 200191102; 384 - 200191103

Automations

Sample Type and Calculate Master Mix - Focus
  • Trigger Location = Record Details

  • Trigger Style = Manual button

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.::Total Samples:: = step.::Total Samples:: + 1' \
-log {compoundOutputFileLuid0} && /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.::Sample Type:: = ::cDNA:: ; \
step.::5X AmpliSeq HiFi Mix (uL):: = 4 * step.::Total Samples:: * 1.1 ; \
step.::5x AmpliSeq Focus Panel (uL):: = 4 * step.::Total Samples:: * 1.1 ; \
step.::Nuclease-free water (uL):: = 2 * step.::Total Samples:: * 1.1' \
-log {compoundOutputFileLuid0}"
Set Next Step - Advance
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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 = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"
Routing Samples
  • Trigger Location = Not Used

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 {compoundOutputFileLuid0} script:changeWorkflow \
\
--FIELD_NAME 'Sample Type' \
--FIELD_VALUE 'cDNA' \
--WORKFLOW 'DNA Library Prep AmpliSeq for Illumina Childhood Cancer Panel v1.1' \
--STEP 'Transfer RNA and DNA Amplicons (AmpliSeq for Illumina Childhood Cancer Panel v1.1)' \
--INPUTS_OR_OUTPUTS 'OUTPUTS' "

ℹ The workflow version and step version for the routing script may vary depending on the version of the IPP.

Sample Type and Calculate Master Mix
  • Trigger Location = Not Used

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.::Total Samples:: = step.::Total Samples:: + 1' \
-log {compoundOutputFileLuid0} && /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.::Sample Type:: = ::cDNA:: ; \
step.::5X AmpliSeq HiFi Mix (uL):: = 4 * step.::Total Samples:: * 1.1 ; \
step.::Nuclease-free water (uL):: = 2 * step.::Total Samples:: * 1.1' \
-log {compoundOutputFileLuid0}"
Set Sample Type and Calculate Master Mix - Immune Repertoire Panel
  • Trigger Location = Not Used

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.::Total Samples:: = step.::Total Samples:: + 1' \
-log {compoundOutputFileLuid0} && /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.::Sample Type:: = ::cDNA:: ; \
step.::5X AmpliSeq HiFi Mix (uL):: = 4.0 * step.::Total Samples:: * 1.1 ; \
step.::5X AmpliSeq Immune Repertoire Panel (uL):: = 4.0 * step.::Total Samples:: * 1.1 ; \
step.::Nuclease-free water (uL):: = 7.0 * step.::Total Samples:: * 1.1' \
-log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Record Details

  • Step Data (Master Step Fields)

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    5x AmpliSeq Focus Panel (uL)

    Numeric

    Decimal Places Displayed = 1

    5X AmpliSeq HiFi Mix (uL)

    Numeric

    Decimal Places Displayed = 1

    Nuclease-free water (uL)

    Numeric

    Decimal Places Displayed = 1

    PCR Cycles

    Numeric

    Decimal Places Displayed = 1

    Thermal Cycler Program

    Text

    Default = AMP

    Total Samples

    Numeric

    Default = 0

  • Step File Placeholders

    • Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

      Container

      LIMS ID (Container)

      Built-in

      Container

      Well

      Built-in

      Derived Sample

      Sample Name

      Built-in

      Project

      Project Name

      Built-in

Step 6: Partially Digest Amplicons (AmpliSeq for Illumina Focus Panel v1.1)

  • Master Step Name = Partially Digested Amplicons (AmpliSeq for Illumina Focus Panel v1.1)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

  • Reagent Kits

    • AmpliSeq cDNA Synthesis for Illumina

      • Supplier = Illumina

      • Catalog Number = 20022654

Automations

Set Next Step - Advance
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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 = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"
Routing cDNA- Focus Panel
  • Trigger Location = Step

  • Trigger Style = Automatic upon exit

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 {compoundOutputFileLuid0} script:changeWorkflow \
\
--FIELD_NAME 'Queue for Plate Transfer' \
--FIELD_VALUE 'Transfer Amplicons' \
--WORKFLOW 'DNA Library Prep AmpliSeq for Illumina Focus Panel v1.1' \
--STEP 'Transfer RNA and DNA Amplicons (AmpliSeq for Illumina Focus Panel v1.1)' \
--INPUTS_OR_OUTPUTS 'OUTPUTS' "

ℹ The workflow version and step version for the routing script may vary depending on the version of the IPP.

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

    Category

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Container

    Container Name

    Built-in

    Container

    LIMS ID (Container)

    Built-in

    Container

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Waiting

    Built-in

    Project

    Project Name

    Built-in

Record Details

  • Step Data (Master Step Fields)

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Thermal Cycler Program

    Text

    Default = FUPA

  • Step File Placeholders

    • Log - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • Table Columns - Global Fields

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

      Container

      LIMS ID (Container)

      Built-in

      Container

      Well

      Built-in

      Derived Sample

      Queue for Plate Transfer

      Text

      Default = Transfer Amplicons

      Derived Sample

      Sample Name

      Built-in

      Project

      Project Name

      Built-in

Website =

Website =

Website =

www.illumina.com
www.illumina.com
www.illumina.com