TruSeq RNA Access v2.0

Overview

The TruSeq RNA Access v2.0 workflow includes the following functionality:

  • Preconfigured TruSeq RNA Access v2.0 protocol that supports the conversion of total RNA or FFPE samples into a library of template molecules 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 workflow.

  • Automatic step transition when required.

  • Automatic placement of samples when necessary.

  • Automated generation of Bioanalyzer input file that the user may upload to the Bioanalyzer instrument’s Expert Software and use to set up a run.

  • Automated parsing of a Bioanalyzer instrument's XML result file into the LIMS, and storing of QC measurement records for the completed run.

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

  • Routing script that allows sequencing of libraries using any Illumina sequencing instrument.

Protocol 1: TruSeq RNA Access v2.0

Protocol Type = Library Prep

Next Steps Configuration

Step 1: Sort Samples (TruSeq RNA Access v2.0)

  • Master Step Name = Sort Samples (TruSeq RNA Access v2.0.10)

  • Step Type = No Outputs

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Record Details

  • Step Data (Master Step Fields)

  • Sample Table

    • Sample Display Default = Collapse

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 2: Fragment RNA (TruSeq RNA Access v2.0)

  • Master Step Name = Fragment RNA v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {SubmittedSampleName}

  • Reagent Kits

    • TruSeq RNA Access - 12 Index Set A or B, Box 2

Automations

Dilute Total 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.::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}"
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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Placement

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

    • Placement Pattern = Row

  • Destination Containers

    • 96 well plate

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 3: First Strand cDNA Synthesis (TruSeq RNA Access v2.0)

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

  • Step Type = No Outputs

  • Reagent Kits

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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

  • Sample Table

    • Column Headers

    • Expanded View Fields

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 4: Second Strand cDNA Synthesis (TruSeq RNA Access v2.0)

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

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {SubmittedSampleName}

  • Reagent Kits

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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • Table Columns - Global Fields

Step 5: Adenylate 3' Ends (TruSeq RNA Access v2.0)

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

  • Step Type = No Outputs

  • Reagent Kits

    • TruSeq RNA Access - 12 Index Set A or B, Box 2

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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Column

    • Table Columns - Global Fields

Step 6: Ligate Adapters (TruSeq RNA Access v2.0)

  • Master Step Name = Ligate Adapters v2.0

  • Step Type = Add Labels

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {SubmittedSampleName}

  • Reagent Kits

    • TruSeq RNA Access - 12 Index Set A or B, Box 2

Automations

Set Next Step - Advance
  • 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 'nextStep = ::ADVANCE::' \
      -log {compoundOutputFileLuid0}"
Copy to Output
  • 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 'output.::Target Insert Size (bp):: = input.::Target Insert Size (bp)::' -log {compoundOutputFileLuid0}"
Set Next Step & Copy to Input
  • 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:: ; output.::Target Insert Size (bp):: = input.::Target Insert Size (bp)::'  -log {compoundOutputFileLuid0}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Add Labels

  • Label Groups

    • TruSeq RNA Access

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 7: First PCR Amplification (TruSeq RNA Access v2.0)

  • Master Step Name = First PCR Amplification (TruSeq RNA Access v2.0.10)

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {SubmittedSampleName}

  • Reagent Kits

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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 8: Bioanalyzer QC (Library Validation) (TruSeq RNA Access v2.0)

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

  • Step Type = Standard QC

  • Measurement Generation = Fixed, 1

  • Naming Convention = {InputItemName} Bioanalyzer

Automations

Generate Bioanalyzer Input file
  • 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/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 '"
Parse Bioanalyzer XML and assign QC flags
  • 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:parseBioAnalyzer -inputFile {compoundOutputFileLuid2} -log {compoundOutputFileLuid5} -configFile '/opt/gls/clarity/extensions/conf/v5/bioanalyzer/defaultBioAnalyzerDNAConfig.groovy' script:assignQC -log {compoundOutputFileLuid6} -qcResult {compoundOutputFileLuid7}"
Parse Bioanalyzer XML, Assign QC flags, and Copy Concentrations
  • 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: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}"
Set Next Step - Output PASS/FAIL
  • 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 true -h false -excludeControls true -exp 'if (output.QC == true) { nextStep = ::ADVANCE:: } else { nextStep = ::ESCALATE:: }' -log {compoundOutputFileLuid0}"
Parse Bioanalyzer XML, Calculate nM and assign QC flags
  • 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 {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}"
Parse Bioanalyzer XML, Copy nM and Assign QC flags
  • 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 {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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table (Column Headers)

Placement = Enabled

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Column

    • Placement Pattern = Column

  • Destination Containers

    • BioAnalyzer DNA High Sensitivity Chip

    • BioAnalyzer DNA 1000 Chip

Record Details

Group of Defaults

Nextera DNA Flex Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

Nextera Mate Pair Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

Nextera XT DNA Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

NRCC Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq ChIP-Seq Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq Exome Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq Methyl Capture EPIC Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 300.00

TruSeq Rapid Exome Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 500.00

TruSeq RNA Access Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 320.00

TruSeq RNA Exome Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 200.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 320.00

TruSeq Small RNA Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq Stranded mRNA Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq Stranded Total RNA Library Validation
  • Criteria 1 - Operator = >=

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

  • 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

TruSeq Targeted RNA Expression Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 100.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 300.00

TruSight Myeloid Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 150.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 400.00

TruSight RNA Fusion Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 160.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 700.00

TSCA Library Validation
  • Criteria 1 - Operator = >=

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

  • Criteria 1 - Threshold Value = 300.00

  • Criteria 2 - Operator = <=

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

  • Criteria 2 - Threshold Value = 400.00

  • Step Data

    • Group of Defaults = TruSeq RNA Access Library Validation

    • Master Step Fields

  • 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

Step 9: First Hybridization (TruSeq RNA Access v2.0)

  • Master Step Name = Hybridize with Pooling v2.0

  • Step Type = Pooling

  • Aliquot Generation = Fixed, 1

  • Naming Convention = {PoolName}

  • Reagent Kits

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}"

Queue/Ice Bucket

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

  • Sample Table

    • Column Headers

    • Expanded View Fields

Pooling

  • Label Uniqueness = On

  • Defaults

    • Sample Grouping = Group by Containers

    • Well Sort Order = Row

Placement

  • Defaults

    • Well Sort Order = Row

    • Placement Pattern = Column

  • Destination Containers

    • 96 well plate

Record Details

  • Step Data (Master Step Fields)

  • Step File Placeholders

    • Log File - Automatically attached

  • Sample Table

    • Sample Display Default = Expand

    • Well Sort Order = Row

    • Table Columns - Global Fields

Step 10: First Capture (TruSeq RNA Access v2.0)

  • Master Step Name = Capture Hybridized Probes v2.0

  • Step Type = Standard

  • Derived Sample Generation = Fixed, 1

  • Naming Convention = {InputItemName}

  • Reagent Kits

Automations

Calculate Master Mix
  • 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: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}"
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}"