JAX-CNV: A Whole-genome Sequencing-based Algorithm for Copy Number Detection at Clinical Grade Level-Reference-Cited by-同舟云学术

JAX-CNV: A Whole-genome Sequencing-based Algorithm for Copy Number Detection at Clinical Grade Level

Published:2022-01 Issue: Volume: Page:
ISSN:1672-0229
Container-title:Genomics, Proteomics & Bioinformatics
language:en
Short-container-title:Genomics, Proteomics & Bioinformatics

Author:

Lee Wan-Ping^ORCID,Zhu Qihui^ORCID,Yang Xiaofei^ORCID,Liu Silvia^ORCID,Cerveira Eliza^ORCID,Ryan Mallory^ORCID,Mil-Homens Adam^ORCID,Bellfy Lauren^ORCID,Ye Kai^ORCID,Lee Charles^ORCID,Zhang Chengsheng^ORCID

Publisher

Elsevier BV

Subject

Computational Mathematics,Genetics,Molecular Biology,Biochemistry

Reference43 articles.

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2. The clinical context of copy number variation in the human genome;Lee;Expert Rev Mol Med,2010

3. Copy-number variation and association studies of human disease;McCarroll;Nat Genet,2007

4. Molecular mechanisms for genomic disorders;Inoue;Annu Rev Genomics Hum Genet,2002

5. Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites;Chen;Obesity,2011

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