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Published November 28, 2016 | Version v0.5.1

hammerlab/isovar: Version 0.5.1

  • 1. Mount Sinai School of Medicine
  • 2. @hammerlab
  • 3. http://ergoso.me

Description

Variant sequences assembled from reads with overlapping sequence content. Matching variant sequences to reference transcripts (to determine reading frame) will iteratively trim the sequence by coverage (to get around low coverage sequence regions with errors).

Files

hammerlab/isovar-v0.5.1.zip

Files (14.0 MB)

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