Cargando…
Long-read sequencing and de novo assembly of a Chinese genome
Short-read sequencing has enabled the de novo assembly of several individual human genomes, but with inherent limitations in characterizing repeat elements. Here we sequence a Chinese individual HX1 by single-molecule real-time (SMRT) long-read sequencing, construct a physical map by NanoChannel arr...
Autores principales: | Shi, Lingling, Guo, Yunfei, Dong, Chengliang, Huddleston, John, Yang, Hui, Han, Xiaolu, Fu, Aisi, Li, Quan, Li, Na, Gong, Siyi, Lintner, Katherine E., Ding, Qiong, Wang, Zou, Hu, Jiang, Wang, Depeng, Wang, Feng, Wang, Lin, Lyon, Gholson J., Guan, Yongtao, Shen, Yufeng, Evgrafov, Oleg V., Knowles, James A., Thibaud-Nissen, Francoise, Schneider, Valerie, Yu, Chack-Yung, Zhou, Libing, Eichler, Evan E., So, Kwok-Fai, Wang, Kai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931320/ https://www.ncbi.nlm.nih.gov/pubmed/27356984 http://dx.doi.org/10.1038/ncomms12065 |
Ejemplares similares
-
SeqMule: automated pipeline for analysis of human exome/genome sequencing data
por: Guo, Yunfei, et al.
Publicado: (2015) -
Identifying disease mutations in genomic medicine settings: current challenges and how to accelerate progress
por: Lyon, Gholson J, et al.
Publicado: (2012) -
“Genotype-first” approaches on a curious case of idiopathic progressive cognitive decline
por: Shi, Lingling, et al.
Publicado: (2014) -
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing data
por: Wei, Zhi, et al.
Publicado: (2011) -
NAA10-related syndrome
por: Wu, Yiyang, et al.
Publicado: (2018)