Article
Identification of indels in next-generation sequencing data.
BMC bioinformatics - 13 Feb 2015
Ratan Aakrosh, Olson Thomas L, Loughran Thomas P, Miller Webb
Abstract excerpt
BACKGROUND: The discovery and mapping of genomic variants is an essential step in most analysis done using sequencing reads. There are a number of mature software packages and associated pipelines that can identify single nucleotide polymorphisms (SNPs) with a high degree of concordance. However, the same cannot be said for tools that are used to identify the other types of variants. Indels represent the second...
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