Cargando…
Whole genome sequencing data of multiple individuals of Pakistani descent
Here we report whole genome sequencing of four individuals (H3, H4, H5, and H6) from a family of Pakistani descent. Whole genome sequencing yielded 1084.92, 894.73, 1068.62, and 1005.77 million mapped reads corresponding to 162.73, 134.21, 160.29, and 150.86 Gb sequence data and 52.49x, 43.29x, 51.7...
Autores principales: | Khan, Shahid Y., Ali, Muhammad, Lee, Mei-Chong W., Ma, Zhiwei, Biswas, Pooja, Khan, Asma A., Naeem, Muhammad Asif, Riazuddin, Saima, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7555865/ https://www.ncbi.nlm.nih.gov/pubmed/33051442 http://dx.doi.org/10.1038/s41597-020-00664-2 |
Ejemplares similares
-
Whole genome sequencing data for two individuals of Pakistani descent
por: Khan, Shahid Y., et al.
Publicado: (2018) -
Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families
por: Nadeem, Raheela, et al.
Publicado: (2020) -
A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
por: Rauf, Bushra, et al.
Publicado: (2016) -
Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family
por: Jiao, Xiaodong, et al.
Publicado: (2019) -
Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families
por: Khan, Shahid Y., et al.
Publicado: (2015)