Genome Sequence Informatics
Repositories for OICR's Genome Sequence Informatics team
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- Toronto, ON
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- mutect2Consensus Public
The Mutect2Consensus workflow will process umiConsensus outputs for the tumour data through mutect2 in tumour only mode to call variants then use information from the matched normal to identify likely germline variants.
oicr-gsi/mutect2Consensus’s past year of commit activity - xenoclassify-workflow Public
workflow to classify short-read sequencing data generated from xenograft samples
oicr-gsi/xenoclassify-workflow’s past year of commit activity - variantMerging Public
a workflow for combining variant calls from SNV analyses done with different callers
oicr-gsi/variantMerging’s past year of commit activity
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