Jointly aligning a group of DNA reads improves accuracy of identifying large deletions.

ABSTRACT: Performing sequence alignment to identify structural variants, such as large deletions, from genome sequencing data is a fundamental task, but current methods are far from perfect. The current practice is to independently align each DNA read to a reference genome. We show that the propensity of genomic rearrangements to accumulate in repeat-rich regions imposes severe ambiguities in these alignments, and consequently on the variant calls-with current read lengths, this affects more than one third of known large deletions in the C. Venter genome. We present a method to jointly align reads to a genome, whereby alignment ambiguity of one read can be disambiguated by other reads. We show this leads to a significant improvement in the accuracy of identifying large deletions (≥20 bases), while i

SUBMITTER: Shrestha AMS 

PROVIDER: S-EPMC5815140 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature