Article

The benefit of a complete reference genome for cancer structural variant analysis

2024-03-18

Abstract excerpt

The complexities of cancer genomes are becoming more easily interpreted due to advancements in sequencing technologies and improved bioinformatic analysis. Structural variants (SVs) represent an important subset of somatic events in tumors. While detection of SVs has been markedly improved by the development of long-read sequencing, somatic variant identification and annotation remains challenging. We hypothesized...

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Literature Corpus work: 030960be-406f-5e78-8d80-d57ff047dd0f
DOI: 10.1101/2024.03.15.24304369

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