Toolkit for robust genomic analyses.
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Subread is a comprehensive toolkit including a fast aligner, exon junction detector (Subjunc), and read summarizer (featureCounts) to support robust genomic analyses.
š Website: Project pageā & GitHubā
š Documentation: Users Guideā
š Citation:
Liao, Y., Smyth, G. K., & Shi, W. (2013). The Subread Aligner: Fast, Accurate and Scalable Read Mapping by Seed-and-Vote. Nucleic Acids Research, 41(10), e108. doi:10.1093/nar/gkt214ā
Content type
Image
Digest
sha256:a06574b25ā¦
Size
242.7 MB
Last updated
over 1 year ago
docker pull willmundlab/subread