ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies

Published:2022-11-01 Issue:3 Volume:31 Page:304-312
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Glessner Joseph T.^ORCID,Li Jin,Liu Yichuan,Khan Munir,Chang Xiao,Sleiman Patrick M. A.,Hakonarson Hakon^ORCID

Funder

U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/s41431-022-01222-7.pdf

Reference25 articles.

1. Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, et al. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res. 2007;17:1665–74.

2. Chang CC, Chow CC, Tellier LC, Vattikuti S, Purcell SM, Lee JJ. Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience 2015;4:7.

3. Glessner JT, Li J, Hakonarson H. ParseCNV integrative copy number variation association software with quality tracking. Nucleic Acids Res. 2013;41:e64.

4. Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009;459:569–73.

5. Mace A, Tuke MA, Beckmann JS, Lin L, Jacquemont S, Weedon MN, et al. New quality measure for SNP array based CNV detection. Bioinformatics 2016;32:3298–305.

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The copy number variant architecture of psychopathology and cognitive development in the ABCD^®study;2024-05-15

2. Genome-wide association studies for economically important traits in mink using copy number variation;Scientific Reports;2024-01-02

3. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders;Journal of Neurodevelopmental Disorders;2023-04-29

4. Genes=disease (?);European Journal of Human Genetics;2023-03

5. ParseCNV2: a versatile and integrated tool for copy number variation association studies;European Journal of Human Genetics;2023-01-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3