GeDi: applying suffix arrays to increase the repertoire of detectable SNVs in tumour genomes
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DOI: 10.1186/s12859-020-3367-3
Abstract: Background Current popular variant calling pipelines rely on the mapping coordinates of each input read to a reference genome in order to detect variants. Since reads deriving from variant loci that diverge in sequence substantially… read more here.
Keywords: mapping coordinates; suffix; repertoire detectable; snv calling ... See more keywords