PGG.SV: a whole-genome-sequencing-based structural variant resource and data analysis platform

Structural variations (SVs) play important roles in human evolution and diseases, but there is a lack of data resources concerning representative samples, especially for East Asians. Taking advantage of both next-generation sequencing and third-generation sequencing data at the whole-genome level, w...

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Detalles Bibliográficos
Autores principales: Wang, Yimin, Ling, Yunchao, Gong, Jiao, Zhao, Xiaohan, Zhou, Hanwen, Xie, Bo, Lou, Haiyi, Zhuang, Xinhao, Jin, Li, Fan, Shaohua, Zhang, Guoqing, Xu, Shuhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Database Issue
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825616/
https://www.ncbi.nlm.nih.gov/pubmed/36243989
http://dx.doi.org/10.1093/nar/gkac905

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825616/
https://www.ncbi.nlm.nih.gov/pubmed/36243989
http://dx.doi.org/10.1093/nar/gkac905

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