STAR aligns short and long RNA-seq reads to a reference genome using
uncompressed suffix arrays, resulting in fast, accurate mapping.
STAR is capable of unbiased de novo detection of canonical splice
junctions, can discover non-canonical splices and chimeric (fusion)
transcripts and can map full-length RNA sequences. Comes with
STARsolo for: mapping, demultiplexing and gene quantification for
single cell RNA-seq (See STARmanual).
Reference: https://www.ncbi.nlm.nih.gov/pubmed/23104886
Maintained by: Rob van Nues
Keywords: read aligner for RNA-seq
ChangeLog: STAR
Homepage:
https://github.com/alexdobin/STAR
Download SlackBuild:
STAR.tar.gz
STAR.tar.gz.asc (FAQ)
(the SlackBuild does not include the source)
Individual Files: |
README |
STAR.SlackBuild |
STAR.info |
slack-desc |
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