Discover hidden splicing variations by mapping personal transcriptomes to personal genomes

November 20, 2015 Leave a comment 9,530 Views

RNA-seq has become a popular technology for studying genetic variation of pre-mRNA alternative splicing. Commonly used RNA-seq aligners rely on the consensus splice site dinucleotide motifs to map reads across splice junctions. Consequently, genomic variants that create novel splice site ...

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Discover hidden splicing variations by mapping personal transcriptomes to personal genomes

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