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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522247/
https://www.ncbi.nlm.nih.gov/pubmed/32985524
http://dx.doi.org/10.1038/s41598-020-71168-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522247/
https://www.ncbi.nlm.nih.gov/pubmed/32985524
http://dx.doi.org/10.1038/s41598-020-71168-7

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