Article
HQAlign: Aligning nanopore reads for SV detection using current-level modeling
2023-01-09
Abstract excerpt
<h4>Motivation</h4> Detection of structural variants (SV) from the alignment of sample DNA reads to the reference genome is an important problem in understanding human diseases. Long reads that can span repeat regions, along with an accurate alignment of these long reads play an important role in identifying novel SVs. Long read sequencers such as nanopore sequencing can address this problem by providing very lon...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 13046925-1033-5c53-95d7-c7df87896c1f
- DOI
- 10.1101/2023.01.08.523172
