Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-analysis of Noncoding Variation in Metabochip Data
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference36 articles.
1. Large-scale whole-genome sequencing of the Icelandic population;Gudbjartsson;Nat. Genet.,2015
2. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010
3. Identifying a high fraction of the human genome to be under selective constraint using GERP++;Davydov;PLoS Comput. Biol.,2010
4. A general framework for estimating the relative pathogenicity of human genetic variants;Kircher;Nat. Genet.,2014
5. A spectral approach integrating functional genomic annotations for coding and noncoding variants;Ionita-Laza;Nat. Genet.,2016
Cited by 45 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 goldmine of GWAS summary statistics: a systematic review of methods and tools;BioData Mining;2024-09-05
2. Meta-analysis of set-based multiple phenotype association test based on GWAS summary statistics from different cohorts;Frontiers in Genetics;2024-09-05
3. Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children;Genes;2024-04-08
4. Accurate and efficient estimation of local heritability using summary statistics and the linkage disequilibrium matrix;Nature Communications;2023-12-02
5. An allelic-series rare-variant association test for candidate-gene discovery;The American Journal of Human Genetics;2023-08
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