Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Allen H. Jiang"'
Autor:
Avinash V. Dharmadhikari, Rajarshi Ghosh, Bo Yuan, Pengfei Liu, Hongzheng Dai, Sami Al Masri, Jennifer Scull, Jennifer E. Posey, Allen H. Jiang, Weimin He, Francesco Vetrini, Alicia A. Braxton, Patricia Ward, Theodore Chiang, Chunjing Qu, Shen Gu, Chad A. Shaw, Janice L. Smith, Seema Lalani, Pawel Stankiewicz, Sau-Wai Cheung, Carlos A. Bacino, Ankita Patel, Amy M. Breman, Xia Wang, Linyan Meng, Rui Xiao, Fan Xia, Donna Muzny, Richard A. Gibbs, Arthur L. Beaudet, Christine M. Eng, James R. Lupski, Yaping Yang, Weimin Bi
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-17 (2019)
Abstract Background Exome sequencing (ES) has been successfully applied in clinical detection of single nucleotide variants (SNVs) and small indels. However, identification of copy number variants (CNVs) using ES data remains challenging. The purpose
Externí odkaz:
https://doaj.org/article/18841bbcba8a49ae8983651c935dcc11
Autor:
Pengfei Liu, Allen H. Jiang, James R. Lupski, Carlos A. Bacino, Jennifer Scull, Seema R. Lalani, Xia Wang, Amy M. Breman, Rajarshi Ghosh, Weimin He, Yaping Yang, Arthur L. Beaudet, Avinash V. Dharmadhikari, Fan Xia, Bo Yuan, Donna M. Muzny, Sami Al Masri, Weimin Bi, Chunjing Qu, Janice L. Smith, Hongzheng Dai, Rui Xiao, Jennifer E. Posey, Shen Gu, Ankita Patel, Sau Wai Cheung, Francesco Vetrini, Linyan Meng, Alicia Braxton, Pawel Stankiewicz, Richard A. Gibbs, Chad A. Shaw, Theodore Chiang, Christine M. Eng, Patricia A. Ward
Publikováno v:
Genome Medicine
Genome Medicine, Vol 11, Iss 1, Pp 1-17 (2019)
Genome Medicine, Vol 11, Iss 1, Pp 1-17 (2019)
Background Exome sequencing (ES) has been successfully applied in clinical detection of single nucleotide variants (SNVs) and small indels. However, identification of copy number variants (CNVs) using ES data remains challenging. The purpose of this