Cargando…
Structural variants in the Chinese population and their impact on phenotypes, diseases and population adaptation
A complete characterization of genetic variation is a fundamental goal of human genome research. Long-read sequencing has improved the sensitivity of structural variant discovery. Here, we conduct the long-read sequencing-based structural variant analysis for 405 unrelated Chinese individuals, with...
Autores principales: | Wu, Zhikun, Jiang, Zehang, Li, Tong, Xie, Chuanbo, Zhao, Liansheng, Yang, Jiaqi, Ouyang, Shuai, Liu, Yizhi, Li, Tao, Xie, Zhi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586011/ https://www.ncbi.nlm.nih.gov/pubmed/34764282 http://dx.doi.org/10.1038/s41467-021-26856-x |
Ejemplares similares
-
High Frequency of AIFM1 Variants and Phenotype Progression of Auditory Neuropathy in a Chinese Population
por: Wang, Hongyang, et al.
Publicado: (2020) -
Genetic variant in IL-33 is associated with idiopathic recurrent miscarriage in Chinese Han population
por: Yue, Jun, et al.
Publicado: (2016) -
Genetic variants in Forkhead box O1 associated with predisposition to sepsis in a Chinese Han population
por: Wang, Huijuan, et al.
Publicado: (2019) -
Single-cell characterization of malignant phenotypes and microenvironment alteration in retinoblastoma
por: Wu, Cheng, et al.
Publicado: (2022) -
Genetic and immune changes in Tibetan high-altitude populations contribute to biological adaptation to hypoxia
por: Bai, Jun, et al.
Publicado: (2022)