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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.
Reference: https://www.ncbi.nlm.nih.gov/pubmed/23104886
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