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Type: New Feature
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Status: Closed
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Priority: Trivial
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Resolution: Won't Fix
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Affects Version/s: 1.14.1
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Fix Version/s: None
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Labels:
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Affect Type:Userdefined
This request is based on a comment from the "Unipro UGENE NGS pipelines and components for variant calling, RNA-seq and ChIP-seq data analyses" paper reviewer.
This would be more beneficial for the biologist and also for easy adaption if authors can Include ready to use best practices workflows. For example:
1. Variant calling work flows for germline and somatic mutations based on additional tools such as GATK, varscan2, FreeBayes for Exome Sequencing.
- relates to
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UGENE-3550 Integrate structural variants analysis workflow
- Closed
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UGENE-3548 Integrate other RNASeq differential expression workflow
- Closed
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UGENE-3549 Integrate workflow for cSNPs
- Closed