SV-HotSpot: detection and visualization of hotspots targeted by structural variants associated with gene expression

Whole genome sequencing (WGS) has enabled the discovery of genomic structural variants (SVs), including those targeting intergenic and intronic non-coding regions that eluded previous exome focused strategies. However, the field currently lacks an automated tool that analyzes SV candidates to identi...

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Publicado no:Sci Rep
Main Authors: Eteleeb, Abdallah M., Quigley, David A., Zhao, Shuang G., Pham, Duy, Yang, Rendong, Dehm, Scott M., Luo, Jingqin, Feng, Felix Y., Dang, Ha X., Maher, Christopher A.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7522247/
https://ncbi.nlm.nih.gov/pubmed/32985524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-71168-7
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