Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

AddOrReplaceReadGroups (Picard) Follow

3 comments

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    kevin yang

    Hi, Could you tell me how can I get a read-group library?I can not find it .

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    Chahat Upreti

    Hi, the link for GATK dictionary entry is missing.

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    Brian Wiley

    AddOrReplaceReadGroups doesn't add an @PG program line for the call to this program.  MarkDuplicates does.  Is there a list of which Picard tools add @PG line for metadata processing and which don't?

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