SVExpress: identifying gene features altered recurrently in expression with nearby structural variant breakpoints

BACKGROUND: Combined whole-genome sequencing (WGS) and RNA sequencing of cancers offer the opportunity to identify genes with altered expression due to genomic rearrangements. Somatic structural variants (SVs), as identified by WGS, can involve altered gene cis-regulation, gene fusions, copy number...

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Detaylı Bibliyografya
Yayımlandı:BMC Bioinformatics
Asıl Yazarlar: Zhang, Yiqun, Chen, Fengju, Creighton, Chad J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2021
Konular:
Software
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7981925/
https://ncbi.nlm.nih.gov/pubmed/33743584
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-021-04072-0
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