A Fast and Noise-Resilient Approach to Detect Rare-Variant Associations With Deep Sequencing Data for Complex Disorders
Author:
Affiliation:
1. Department of Biostatistics; Mailman School of Public Health; Columbia University; New York; New York
2. Department of Molecular and Human Genetics; Baylor College of Medicine; Houston; Texas
Publisher
Wiley
Subject
Genetics (clinical),Epidemiology
Reference38 articles.
1. Medical sequencing at the extremes of human body mass;Ahituv;Am J Hum Genet,2007
2. Statistical Methods in Medical Research
3. Statistical analysis strategies for association studies involving rare variants;Bansal;Nat Rev Genet,2010
4. On alleged gains in power from lower P-values;Barnard;Stat Med,1989
5. A covering method for detecting genetic associations between rare variants and common phenotypes;Bhatia;PLoS Comput Biol,2010
Cited by 20 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. Excalibur: A new ensemble method based on an optimal combination of aggregation tests for rare-variant association testing for sequencing data;PLOS Computational Biology;2023-09-14
2. An Integrative Approach to Analyze Seed Germination in Brassica napus;Frontiers in Plant Science;2019-10-25
3. Association detection between ordinal trait and rare variants based on adaptive combination of P values;Journal of Human Genetics;2017-11-07
4. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease;PLOS ONE;2017-07-24
5. Selection Probability for Rare Variant Association Studies;Journal of Computational Biology;2017-05
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