Article

Precise characterization of somatic complex structural variations from paired long-read sequencing data with nanomonsv

2020-07-23

Abstract excerpt

We present our novel software, nanomonsv, for detecting somatic structural variations (SVs) using tumor and matched control long-read sequencing data with a single-base resolution. The current version of nanomonsv includes two detection modules, Canonical SV module, and Single breakend SV module. Using paired long-read sequencing data from three cancer and their matched lymphoblastoid lines, we demonstrate that Ca...

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Literature Corpus work: f5cdd974-42c6-5d41-96ff-230007f1a0f9
DOI: 10.1101/2020.07.22.214262

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