11 lines
494 B
Plaintext
11 lines
494 B
Plaintext
STAR aligns short and long RNA-seq reads to a reference genome using
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uncompressed suffix arrays, resulting in fast, accurate mapping.
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STAR is capable of unbiased de novo detection of canonical splice
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junctions, can discover non-canonical splices and chimeric (fusion)
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transcripts and can map full-length RNA sequences. Comes with
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STARsolo for: mapping, demultiplexing and gene quantification for
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single cell RNA-seq (See STARmanual).
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Reference: https://www.ncbi.nlm.nih.gov/pubmed/23104886
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