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TruSeq RNA Exome v1.0

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Overview

TruSeq RNA Exome v1.0 includes the following functionality:

  • Preconfigured TruSeq RNA Exome v1.0 protocol that explains how to convert total RNA into a library of template molecules of known strand origin, then capture the coding regions of the transcriptome using the reagents provided in Illumina® TruSeq® RNA Access Library Prep kits. The resulting library is suitable for subsequent cluster generation and sequencing.

  • Automated calculation of sample and buffer volumes.

  • Automated calculation or display of reagents at every step in the protocol.

  • Automatic step transition when required.

  • Automatic placement of samples when necessary.

  • Automated assignment of QC Pass/Fail, based on user-selected threshold values.

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Protocol 1: TruSeq RNA Exome v1.0

Protocol Type = Library Prep

Next Steps Configuration

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Step 1: Fragment RNA (TruSeq RNA Exome v1.0)

  • Master Step Name = Fragment RNA v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {SubmittedSampleName}

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Automations

chevron-rightDilute Total RNAhashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 2: Synthesize First Strand cDNA (TruSeq RNA Exome v1.0)

  • Master Step Name = First Strand cDNA Synthesis v2.0

  • Step Type = No Outputs

  • Reagent Kits

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

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Record Details

  • Step Data (Master Step Fields)

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Step 3: Synthesize Second Strand cDNA (TruSeq RNA Exome v1.0)

  • Master Step Name = Second Strand cDNA Synthesis v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 4: Adenylate 3' Ends (TruSeq RNA Exome v1.0)

  • Master Step Name = Adenylate 3' Ends v2.0

  • Step Type = No Outputs

  • Reagent Kits

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 5: Ligate Adapters (TruSeq RNA Exome v1.0)

  • Master Step Name = Ligate Adapters v2.0

  • Step Type = Add Labels

  • Derived Sample Generation = Fixed, 1

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightCopy to Outputhashtag
  • Trigger Location = Not Used

chevron-rightSet Next Step & Copy to Inputhashtag
  • Trigger Location = Not Used

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Add Labels

  • Label Groups

    • TruSeq RNA Single Indexes (12 indexes, 24 samples) Set A

    • TruSeq RNA Single Indexes (12 indexes, 24 samples) Set B

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Record Details

  • Step Data (Master Step Fields)

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Step 6: Enrich DNA Fragments (TruSeq RNA Exome v1.0)

  • Master Step Name = Enrich DNA Fragments (TruSeq RNA Exome v1.0.6)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 7: Bioanalyzer QC (Library Validation) (TruSeq RNA Exome v1.0)

  • Master Step Name = Bioanalyzer QC (Library Validation) v2.0

  • Step Type = Standard QC

  • Measurement Generation = Fixed, 1

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Automations

chevron-rightGenerate Bioanalyzer Input filehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

chevron-rightParse Bioanalyzer XML and assign QC flagshashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightSet Next Step - Output PASS/FAILhashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightParse Bioanalyzer XML, Assign QC flags, and Copy Concentrationshashtag
  • Trigger Location = Not Used

chevron-rightParse Bioanalyzer XML, Calculate nM and assign QC flagshashtag
  • Trigger Location = Not Used

chevron-rightParse Bioanalyzer XML, Copy nM and Assign QC flagshashtag
  • Trigger Location = Not Used

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

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Record Details

Group of Defaults

chevron-rightNextera DNA Flex Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightNextera Mate Pair Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightNextera XT DNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightNRCC Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq ChIP-Seq Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Methyl Capture EPIC Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Rapid Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq RNA Access Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq RNA Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Small RNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Stranded mRNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Stranded Total RNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Targeted RNA Expression Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSight Myeloid Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSight RNA Fusion Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTSCA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

  • Step Data

    • Group of Defaults = TruSeq RNA Exome Library Validation

    • Master Step Fields

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Step 8: Hybridize Probes (TruSeq RNA Exome v1.0)

  • Master Step Name = Hybridize with Pooling v2.0

  • Step Type = Pooling

  • Aliquot Generation = Fixed, 1

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Pooling

  • Label Uniqueness = On

  • Defaults

    • Sample Grouping = Group by Containers

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Placement = Enabled

  • Defaults

    • Well Sort Order = Row

    • Placement Pattern = Column

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Record Details

  • Step Data (Master Step Fields)

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Step 9: Capture Hybridized Probes (TruSeq RNA Exome v1.0)

  • Master Step Name = Capture Hybridized Probes v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

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Automations

chevron-rightCalculate Master Mixhashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 10: Second Hybridization (TruSeq RNA Exome v1.0)

  • Master Step Name = Perform Second Hybridization v2.0

  • Step Type = No Outputs

  • Reagent Kits

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 11: Second Capture (TruSeq RNA Exome v1.0)

  • Master Step Name = Perform Second Capture v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 12: Clean Up Captured Library (TruSeq RNA Exome v1.0)

  • Master Step Name = Clean Up v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 13: Amplify Enriched Library (TruSeq RNA Exome v1.0)

  • Master Step Name = Second PCR Amplification v1.0

  • Step Type = No Outputs

  • Reagent Kits

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 14: Clean Up Amplified Enriched Library (TruSeq RNA Exome v1.0)

  • Master Step Name = Clean Up v2.0

  • Step Type = Standard

  • Reagent Kits

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Automations

chevron-rightSet Next Step - Advancehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Record Details

  • Step Data (Master Step Fields)

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Step 15: Bioanalyzer QC (Library Validation) (TruSeq RNA Exome v1.0)

  • Master Step Name = Bioanalyzer QC (Library Validation) v2.0

  • Step Type = Standard QC

  • Measurement Generation = Fixed, 1

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Automations

chevron-rightGenerate Bioanalyzer Input filehashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon entry

chevron-rightParse Bioanalyzer XML, Calculate nM and assign QC flagshashtag
  • Trigger Location = Record Details

  • Trigger Style = Manual button

chevron-rightSet Next Step - Output PASS/FAILhashtag
  • Trigger Location = Record Details

  • Trigger Style = Automatic upon exit

chevron-rightParse Bioanalyzer XML and assign QC flagshashtag
  • Trigger Location = Not Used

chevron-rightParse Bioanalyzer XML, Assign QC flags, and Copy Concentrationshashtag
  • Trigger Location = Not Used

chevron-rightParse Bioanalyzer XML, Copy nM and Assign QC flagshashtag
  • Trigger Location = Not Used

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Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

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Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

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Record Details

Group of Defaults

chevron-rightNextera DNA Flex Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightNextera Mate Pair Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightNextera XT DNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightNRCC Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq ChIP-Seq Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Methyl Capture EPIC Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Rapid Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq RNA Access Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq RNA Exome Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSeq Small RNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Stranded mRNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Stranded Total RNA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSeq Targeted RNA Expression Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Peak 2 Size - bp

chevron-rightTruSight Myeloid Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTruSight RNA Fusion Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

chevron-rightTSCA Library Validationhashtag
  • Criteria 1 - Operator = >=

  • Criteria 1 - Source Data Field = Region 1 Average Size - bp

  • Step Data

    • Group of Defaults = TruSeq RNA Exome Library Validation

    • Master Step Fields

  • Reagent Kits

    • TruSeq RNA Library Prep for Enrichment

      • Supplier = Illumina

      • Catalog Number = 20020189

      • Website =

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Decimal Places Displayed = 1

    Thermal Cycler Program

    Text

    Default = Elution 2 - Frag - Prime

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • SuperScript II Reverse Transcriptase
    • Supplier = Life Technologies

    • Catalog Number = 18064-014

    • Website = http://www.lifetechnologies.com/order/catalog/product/18064014arrow-up-right

  • TruSeq RNA Library Prep for Enrichment

    • Supplier = Illumina

    • Catalog Number = 20020189

    • Website =

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    • Presets

      • Synthesize 1st Strand

      • 1stSS

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {SubmittedSampleName}
  • Reagent Kits

    • AMPure XP Beads

      • Supplier = Beckman Coulter Genomics

      • Catalog Number = A63881

      • Website =

    • TruSeq RNA Library Prep for Enrichment

      • Supplier = Illumina

      • Catalog Number = 20020189

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • Table Columns - Global Fields

  • TruSeq RNA Library Prep for Enrichment
    • Supplier = Illumina

    • Catalog Number = 20020189

    • Website = www.illumina.comarrow-up-right

    Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    RSB to add to each well (uL)

    Numeric

    Default = 2.5

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • Table Columns - Global Fields

  • Naming Convention = {SubmittedSampleName}
  • Reagent Kits

    • AMPure XP Beads

      • Supplier = Beckman Coulter Genomics

      • Catalog Number = A63881

      • Website =

    • TruSeq RNA Library Prep for Enrichment

      • Supplier = Illumina

      • Catalog Number = 20020189

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Default = 42

    Round 1 RSB to each well (uL)

    Numeric

    Default = 52.5

    Round 2 EtOH to each well (uL)

    Numeric

    Default = 50

    Round 2 RSB to each well (uL)

    Numeric

    Default = 22.5

    1 RSB to add to each well (uL)

    Numeric

    Default = 2.5

    2 LIG to add to each well (uL)

    Numeric

    Default = 2.5

    3 RNA Adapters to add to each well (uL)

    Numeric

    Default = 2.5

    80% EtOH Prep Date

    Date

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {SubmittedSampleName}
  • Reagent Kits

    • AMPure XP Beads

      • Supplier = Beckman Coulter Genomics

      • Catalog Number = A63881

      • Website =

    • TruSeq RNA Library Prep Enrichment Component, Box 1

      • Supplier = Illumina

      • Catalog Number = 20020490

    • TruSeq RNA Library Prep for Enrichment

      • Supplier = Illumina

      • Catalog Number = 20020189

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Default = PCR

    80% EtOH Prep Date

    Date

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {InputItemName} Bioanalyzer
    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

    Placement Pattern = Column
  • Destination Containers

    • BioAnalyzer DNA High Sensitivity Chip

    • BioAnalyzer DNA 1000 Chip

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,500.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 250.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 350.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 300.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 500.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 320.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 320.00

  • Criteria 1 - Threshold Value = 100.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 200.00

  • Criteria 1 - Threshold Value = 250.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 275.00

  • Criteria 1 - Threshold Value = 250.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 275.00

  • Criteria 1 - Threshold Value = 100.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 300.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 160.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 700.00

  • Criteria 1 - Threshold Value = 300.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Options

    Additional Options and Dropdown Items

    Criteria 1 - Operator

    Text Dropdown

    Custom Entries

    Presets

    • >=

    • <=

    • =

    Criteria 1 - Source Data Field

    Text Dropdown

    Presets

    • Concentration

    • Conc. Units

    • Number of Peaks found

    Criteria 1 - Threshold Value

    Numeric

    Decimal Places Displayed = 2

    Criteria 2 - Operator

    Text Dropdown

    Custom Entries

    Presets

    • >=

    • <=

    • =

    Criteria 2 - Source Data Field

    Text Dropdown

    Presets

    • Concentration

    • Conc. Units

    • Number of Peaks found

    Criteria 2 - Threshold Value

    Numeric

    Decimal Places Displayed = 2

    Use strict matching for Bioanalyzer results

    Toggle Switch

    Default = None Set

  • Step File Placeholders

    • Bioanalyzer Input File - Automatically attached

    • Bioanalyzer Input File Generation Log File - Automatically attached

    • Bioanalyzer XML Result File (required) - Manually uploaded

    • Result File (optional) - Manually uploaded

    • PDF Summary File (optional) - Manually uploaded

    • Bioanalyzer XML Parsing Log File - Automatically attached

    • QC Assignment Log File - Automatically attached

    • QC Assignment Report - Automatically attached

  • Sample Table

    • Enable QC Flags = Yes

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • File Column Options

      • File Column Display = Hide

      • File Attachment Method = Auto

    • Table Columns - Global Fields

  • Naming Convention = {PoolName}
  • Reagent Kits

    • TruSeq RNA Library Prep Coding Exome Oligos

      • Supplier = Illumina

      • Catalog Number = 20020183

      • Website =

    • TruSeq RNA Library Prep Enrichment Component, Box 2

      • Supplier = Illumina

      • Catalog Number = 20020490

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Well Sort Order = Row
    Destination Containers
    • 96 well plate

    Presets

    • RNA HYB

    • NRC HYB

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {InputItemName}
  • Reagent Kits

    • TruSeq RNA Library Prep Enrichment Component, Box 1

      • Supplier = Illumina

      • Catalog Number = 20020490

      • Website =

    • TruSeq RNA Library Prep Enrichment Component, Box 2

      • Supplier = Illumina

      • Catalog Number = 20020490

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Decimal Places Displayed = 2

    2N NaOH (ul)

    Numeric

    Decimal Places Displayed = 2

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • TruSeq RNA Library Prep Coding Exome Oligos
    • Supplier = Illumina

    • Catalog Number = 20020183

    • Website = www.illumina.comarrow-up-right

  • TruSeq RNA Library Prep Enrichment Component, Box 2

    • Supplier = Illumina

    • Catalog Number = 20020490

    • Website =

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Default = RNA HYB

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {InputItemName}
  • Reagent Kits

    • TruSeq RNA Library Prep Enrichment Component, Box 1

      • Supplier = Illumina

      • Catalog Number = 20020490

      • Website =

    • TruSeq RNA Library Prep Enrichment Component, Box 2

      • Supplier = Illumina

      • Catalog Number = 20020490

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Step File Placeholders
    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Reagent Kits

    • AMPure XP Beads

      • Supplier = Beckman Coulter Genomics

      • Catalog Number = A63881

      • Website =

    • TruSeq RNA Library Prep Enrichment Component, Box 2

      • Supplier = Illumina

      • Catalog Number = 20020490

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • TruSeq RNA Library Prep Enrichment Component, Box 2
    • Supplier = Illumina

    • Catalog Number = 20020490

    • Website = www.illumina.comarrow-up-right

    Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

    Default = EPM AMP

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • AMPure XP Beads
    • Supplier = Beckman Coulter Genomics

    • Catalog Number = A63881

    • Website = https://www.beckmancoulter.com/wsrportal/wsr/research-and-discovery/products-and-services/nucleic-acid-sample-preparation/agencourt-ampure-xp-pcr-purification/index.htmarrow-up-right

  • TruSeq RNA Library Prep Enrichment Component, Box 2

    • Supplier = Illumina

    • Catalog Number = 20020490

    • Website =

  • Sample Table
    • Column Headers

      Category

      Field Name

      Field Type

      Options

      Additional Options and Dropdown Items

      Container

      Container Name

      Built-in

    • Expanded View Fields

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

  • Naming Convention = {InputItemName} Bioanalyzer
    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

    Placement Pattern = Column
  • Destination Containers

    • BioAnalyzer DNA High Sensitivity Chip

    • BioAnalyzer DNA 1000 Chip

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,500.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 250.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 350.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 1,000.00

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 300.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 500.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 320.00

  • Criteria 1 - Threshold Value = 200.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 320.00

  • Criteria 1 - Threshold Value = 100.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 200.00

  • Criteria 1 - Threshold Value = 250.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 275.00

  • Criteria 1 - Threshold Value = 250.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Average Size - bp

  • Criteria 2 - Threshold Value = 275.00

  • Criteria 1 - Threshold Value = 100.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Peak 2 Size - bp

  • Criteria 2 - Threshold Value = 300.00

  • Criteria 1 - Threshold Value = 150.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Criteria 1 - Threshold Value = 160.00

  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 700.00

  • Criteria 1 - Threshold Value = 300.00
  • Criteria 2 - Operator = <=

  • Criteria 2 - Source Data Field = Region 1 Size - bp

  • Criteria 2 - Threshold Value = 400.00

  • Options

    Additional Options and Dropdown Items

    Criteria 1 - Operator

    Text Dropdown

    Custom Entries

    Presets

    • >=

    • <=

    • =

    Criteria 1 - Source Data Field

    Text Dropdown

    Presets

    • Concentration

    • Conc. Units

    • Number of Peaks found

    Criteria 1 - Threshold Value

    Numeric

    Decimal Places Displayed = 2

    Criteria 2 - Operator

    Text Dropdown

    Custom Entries

    Presets

    • >=

    • <=

    • =

    Criteria 2 - Source Data Field

    Text Dropdown

    Presets

    • Concentration

    • Conc. Units

    • Number of Peaks found

    Criteria 2 - Threshold Value

    Numeric

    Decimal Places Displayed = 2

    Use strict matching for Bioanalyzer results

    Toggle Switch

    Default = None Set

  • Step File Placeholders

    • Bioanalyzer Input File - Automatically attached

    • Bioanalyzer Input File Generation Log File - Automatically attached

    • Bioanalyzer XML Result File (required) - Manually uploaded

    • Result File (optional) - Manually uploaded

    • PDF Summary File (optional) - Manually uploaded

    • Bioanalyzer XML Parsing Log File - Automatically attached

    • QC Assignment Log File - Automatically attached

    • QC Assignment Report - Automatically attached

  • Sample Table

    • Enable QC Flags = Yes

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • File Column Options

      • File Column Display = Hide

      • File Attachment Method = Auto

    • Table Columns - Global Fields

  • Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Desired Diluted Concentration (ng/uL)

    Numeric

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Thermal Cycler Program

    Text Dropdown

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    80% EtOH Prep Date

    Date

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    ATL to add to each well (uL)

    Numeric

    Default = 12.5

    Comment

    Multiline Text

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Round 1 EtOH to each well (uL)

    Numeric

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Thermal Cycler Program

    Text

    Field Name

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Thermal Cycler Program

    Text Dropdown

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Enrichment Elution Buffer 1 (ul)

    Numeric

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Thermal Cycler Program RNA Exome

    Text

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    80% EtOH Prep Date

    Date

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    Thermal Cycler Program

    Text

    Field Name

    Field Type

    Options

    Additional Options and Dropdown Items

    Comment

    Multiline Text

    80% EtOH Prep Date

    Date

    Field Name

    Required Field

    Custom Entries

    Field Type

    Custom Entries

    Field Type

    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.::Sample Volume (ul):: = (step.::Desired Diluted Concentration (ng/uL):: * 8.5) / input.::Concentration:: ; output.::Buffer Volume (ul):: = 8.5 - output.::Sample Volume (ul):: ; output.::Concentration:: = input.::Concentration:: ; output.::Conc. Units:: = input.::Conc. Units::' -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} script:evaluateDynamicExpression -t false -h false -exp 'output.::Target Insert Size (bp):: = input.::Target Insert Size (bp)::' -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} script:evaluateDynamicExpression -t false -h false -exp 'nextStep = ::ADVANCE:: ; output.::Target Insert Size (bp):: = input.::Target Insert Size (bp)::'  -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -log {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar script:driver_file_generator -i {processURI:v2} -u {username} -p {password} -t /opt/gls/clarity/extensions/ngs-common/v5/EPP/conf/readonly/bioA_driver_file_template.csv -o {compoundOutputFileLuid0}.csv -l {compoundOutputFileLuid1}  && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:addBlankLines -i {stepURI:v2} -u {username} -p {password} -f {compoundOutputFileLuid0}.csv -l {compoundOutputFileLuid1} -sep COMMA -b ',False,' -h 1 -c LIMSID -pre 'Sample '"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' script:assignQC -log {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
    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 -excludeControls true -exp 'if (output.QC == true) { nextStep = ::ADVANCE:: } else { nextStep = ::ESCALATE:: }' -log {compoundOutputFileLuid0}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' script:assignQC -log {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7} && /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.::Concentration:: = output.::Region 1 Conc.:: ; input.::Concentration:: = output.::Concentration:: ; output.::Conc. Units:: = ::ng/ul:: ; input.::Conc. Units:: = output.::Conc. Units::' -log {compoundOutputFileLuid8}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' && /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.::Concentration:: = output.::Region 1 Conc.:: ; output.::Molarity (nM):: = (output.::Concentration:: * 1000000) / (660 * output.::Region 1 Average Size - bp::) ; input.::Molarity (nM):: = output.::Molarity (nM):: ; output.::Conc. Units:: = ::ng/ul::' -log {compoundOutputFileLuid8} && /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 {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' && /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 (output.::Conc. Units::.contains(::pg::)) {output.::Molarity (nM):: = output.::Region 1 Molarity:: / 1000} else {output.::Molarity (nM):: = output.::Region 1 Molarity::} ; (input.::Molarity (nM):: = output.::Molarity (nM)::) ' -log {compoundOutputFileLuid8} && /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 {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
    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}"
    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 -t false -h false -exp 'step.::Total Number of Samples:: = step.::Total Number of Samples:: + 1' -log {compoundOutputFileLuid0} && /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 -t false -h false -exp 'step.::Enrichment Elution Buffer 1 (ul):: = 28.5 * step.::Total Number of Samples:: ; step.::2N NaOH (ul):: = 1.5 * step.::Total Number of Samples::' -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -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} \
          script:evaluateDynamicExpression \
          -t false \
          -h false \
          -exp 'nextStep = ::ADVANCE::' \
          -log {compoundOutputFileLuid0}"
    bash -l -c "/opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/DriverFileGenerator.jar script:driver_file_generator -i {processURI:v2} -u {username} -p {password} -t /opt/gls/clarity/extensions/ngs-common/v5/EPP/conf/readonly/bioA_driver_file_template.csv -o {compoundOutputFileLuid0}.csv -l {compoundOutputFileLuid1}  && /opt/gls/clarity/bin/java -jar /opt/gls/clarity/extensions/ngs-common/v5/EPP/ngs-extensions.jar script:addBlankLines -i {stepURI:v2} -u {username} -p {password} -f {compoundOutputFileLuid0}.csv -l {compoundOutputFileLuid1} -sep COMMA -b ',False,' -h 1 -c LIMSID -pre 'Sample '"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' && /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.::Concentration:: = output.::Region 1 Conc.:: ; output.::Molarity (nM):: = (output.::Concentration:: * 1000000) / (660 * output.::Region 1 Average Size - bp::) ; input.::Molarity (nM):: = output.::Molarity (nM):: ; output.::Conc. Units:: = ::ng/ul::' -log {compoundOutputFileLuid8} && /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 {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
    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 -excludeControls true -exp 'if (output.QC == true) { nextStep = ::ADVANCE:: } else { nextStep = ::ESCALATE:: }' -log {compoundOutputFileLuid0}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' script:assignQC -log {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' script:assignQC -log {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7} && /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.::Concentration:: = output.::Region 1 Conc.:: ; input.::Concentration:: = output.::Concentration:: ; output.::Conc. Units:: = ::ng/ul:: ; input.::Conc. Units:: = output.::Conc. Units::' -log {compoundOutputFileLuid8}"
    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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' && /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 (output.::Conc. Units::.contains(::pg::)) {output.::Molarity (nM):: = output.::Region 1 Molarity:: / 1000} else {output.::Molarity (nM):: = output.::Region 1 Molarity::} ; (input.::Molarity (nM):: = output.::Molarity (nM)::) ' -log {compoundOutputFileLuid8} && /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 {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"

    Built-in

    Well

    Built-in

    Derived Sample

    Buffer Volume (ul)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    Concentration

    Numeric

    Required Field

    Decimal Places Displayed = 2

    Derived Sample

    Conc. Units

    Text

    Required Field

    Derived Sample

    Sample Name

    Built-in

    Derived Sample

    Sample Volume (ul)

    Numeric

    Decimal Places Displayed = 2

    Project

    Project Name

    Built-in

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    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Website =

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    Sample Name

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    Project Name

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    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Website =

    Built-in

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    Built-in

    Derived Sample

    Reagent Name

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Website = www.illumina.comarrow-up-right
    Website =

    Built-in

    Well

    Built-in

    Derived Sample

    Sample Name

    Built-in

    Project

    Project Name

    Built-in

    Built-in

    Measurement

    BA Sample Name

    Text

    Measurement

    Concentration

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Conc. Units

    Text

    Measurement

    Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Number of Peaks found

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Number of Regions found

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 1 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 1 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 1 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 2 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 2 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 2 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 3 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 3 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 3 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 4 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 4 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 4 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 5 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 5 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 5 Size - bp

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 1 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 1 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 1 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 2 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 2 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 2 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 3 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 3 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 3 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 4 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 4 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 4 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 5 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 5 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 5 Molarity

    Numeric

    Decimal Places Displayed = 2

    Website = www.illumina.comarrow-up-right

    Built-in

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    Derived Sample

    Sample Name

    Built-in

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    Project Name

    Built-in

    Website = www.illumina.comarrow-up-right

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    Sample Name

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    Built-in

    Website = www.illumina.comarrow-up-right

    Built-in

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    Sample Name

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    Project Name

    Built-in

    Website = www.illumina.comarrow-up-right

    Built-in

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    Sample Name

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    Measurement

    BA Sample Name

    Text

    Measurement

    Concentration

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Conc. Units

    Text

    Measurement

    Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Number of Peaks found

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Number of Regions found

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 1 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 1 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 1 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 2 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 2 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 2 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 3 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 3 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 3 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 4 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 4 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 4 Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Peak 5 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 5 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Peak 5 Size - bp

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 1 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 1 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 1 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 2 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 2 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 2 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 3 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 3 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 3 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 4 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 4 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 4 Molarity

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 5 Average Size - bp

    Numeric

    Decimal Places Displayed = 0

    Measurement

    Region 5 Conc.

    Numeric

    Decimal Places Displayed = 2

    Measurement

    Region 5 Molarity

    Numeric

    Decimal Places Displayed = 2

    Default = Synthesize 1st Strand

    !=

    Peak 1 Size - bp

  • Peak 1 Conc.

  • Peak 1 Molarity

  • Peak 2 Size - bp

  • Peak 2 Conc.

  • Peak 2 Molarity

  • Peak 3 Size - bp

  • Peak 3 Conc.

  • Peak 3 Molarity

  • Peak 4 Size - bp

  • Peak 4 Conc.

  • Peak 4 Molarity

  • Peak 5 Size - bp

  • Peak 5 Conc.

  • Peak 5 Molarity

  • Number of Regions found

  • Region 1 Average Size - bp

  • Region 1 Conc.

  • Region 1 Molarity

  • Region 2 Average Size - bp

  • Region 2 Conc.

  • Region 2 Molarity

  • Region 3 Average Size - bp

  • Region 3 Conc.

  • Region 3 Molarity

  • Region 4 Average Size - bp

  • Region 4 Conc.

  • Region 4 Molarity

  • Region 5 Average Size - bp

  • Region 5 Conc.

  • Region 5 Molarity

  • !=

    Peak 1 Size - bp

  • Peak 1 Conc.

  • Peak 1 Molarity

  • Peak 2 Size - bp

  • Peak 2 Conc.

  • Peak 2 Molarity

  • Peak 3 Size - bp

  • Peak 3 Conc.

  • Peak 3 Molarity

  • Peak 4 Size - bp

  • Peak 4 Conc.

  • Peak 4 Molarity

  • Peak 5 Size - bp

  • Peak 5 Conc.

  • Peak 5 Molarity

  • Number of Regions found

  • Region 1 Average Size - bp

  • Region 1 Conc.

  • Region 1 Molarity

  • Region 2 Average Size - bp

  • Region 2 Conc.

  • Region 2 Molarity

  • Region 3 Average Size - bp

  • Region 3 Conc.

  • Region 3 Molarity

  • Region 4 Average Size - bp

  • Region 4 Conc.

  • Region 4 Molarity

  • Region 5 Average Size - bp

  • Region 5 Conc.

  • Region 5 Molarity

  • !=

    Peak 1 Size - bp

  • Peak 1 Conc.

  • Peak 1 Molarity

  • Peak 2 Size - bp

  • Peak 2 Conc.

  • Peak 2 Molarity

  • Peak 3 Size - bp

  • Peak 3 Conc.

  • Peak 3 Molarity

  • Peak 4 Size - bp

  • Peak 4 Conc.

  • Peak 4 Molarity

  • Peak 5 Size - bp

  • Peak 5 Conc.

  • Peak 5 Molarity

  • Number of Regions found

  • Region 1 Average Size - bp

  • Region 1 Conc.

  • Region 1 Molarity

  • Region 2 Average Size - bp

  • Region 2 Conc.

  • Region 2 Molarity

  • Region 3 Average Size - bp

  • Region 3 Conc.

  • Region 3 Molarity

  • Region 4 Average Size - bp

  • Region 4 Conc.

  • Region 4 Molarity

  • Region 5 Average Size - bp

  • Region 5 Conc.

  • Region 5 Molarity

  • !=

    Peak 1 Size - bp

  • Peak 1 Conc.

  • Peak 1 Molarity

  • Peak 2 Size - bp

  • Peak 2 Conc.

  • Peak 2 Molarity

  • Peak 3 Size - bp

  • Peak 3 Conc.

  • Peak 3 Molarity

  • Peak 4 Size - bp

  • Peak 4 Conc.

  • Peak 4 Molarity

  • Peak 5 Size - bp

  • Peak 5 Conc.

  • Peak 5 Molarity

  • Number of Regions found

  • Region 1 Average Size - bp

  • Region 1 Conc.

  • Region 1 Molarity

  • Region 2 Average Size - bp

  • Region 2 Conc.

  • Region 2 Molarity

  • Region 3 Average Size - bp

  • Region 3 Conc.

  • Region 3 Molarity

  • Region 4 Average Size - bp

  • Region 4 Conc.

  • Region 4 Molarity

  • Region 5 Average Size - bp

  • Region 5 Conc.

  • Region 5 Molarity

  • Container

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    Molarity (nM)

    Numeric

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    Molarity (nM)

    Numeric

    Decimal Places Displayed = 2

    Derived Sample

    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right
    https://www.beckmancoulter.com/wsrportal/wsr/research-and-discovery/products-and-services/nucleic-acid-sample-preparation/agencourt-ampure-xp-pcr-purification/index.htmarrow-up-right
    https://www.beckmancoulter.com/wsrportal/wsr/research-and-discovery/products-and-services/nucleic-acid-sample-preparation/agencourt-ampure-xp-pcr-purification/index.htmarrow-up-right
    https://www.beckmancoulter.com/wsrportal/wsr/research-and-discovery/products-and-services/nucleic-acid-sample-preparation/agencourt-ampure-xp-pcr-purification/index.htmarrow-up-right
    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right
    https://www.beckmancoulter.com/wsrportal/wsr/research-and-discovery/products-and-services/nucleic-acid-sample-preparation/agencourt-ampure-xp-pcr-purification/index.htmarrow-up-right
    www.illumina.comarrow-up-right

    Project Name

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    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right
    www.illumina.comarrow-up-right