Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein‐Coding Regions-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein‐Coding Regions

Published:2015-06-11 Issue:8 Volume:36 Page:815-822
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Lelieveld Stefan H.¹,Spielmann Malte²³,Mundlos Stefan²³,Veltman Joris A.¹⁴,Gilissen Christian¹

Affiliation:

1. Department of Human Genetics Radboud Institute for Molecular Life Sciences Radboud University Medical Center Nijmegen 6525 GA The Netherlands

2. Institute for Medical Genetics and Human Genetics Charité Universitätsmedizin Berlin Berlin Germany

3. Max Planck Institute for Molecular Genetics Berlin Germany

4. Department of Clinical Genetics Maastricht University Medical Centre Maastricht The Netherlands

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

European Research Council

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.22813

Reference42 articles.

1. Accurate and comprehensive sequencing of personal genomes

2. Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities

3. Summarizing and correcting the GC content bias in high-throughput sequencing

4. Performance comparison of exome DNA sequencing technologies

5. Clinical Interpretation and Implications of Whole-Genome Sequencing

Cited by 157 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. Invasive Prenatal Diagnostics: A Cornerstone of Perinatal Management;Applied Sciences;2024-08-07

2. Genome Sequencing for Diagnosing Rare Diseases;New England Journal of Medicine;2024-06-06

3. The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know;Children;2024-05-10

4. Low-frequency and rare genetic variants associated with rheumatoid arthritis risk;Nature Reviews Rheumatology;2024-03-27

5. Genetic interrogation for sequence and copy number variants in systemic lupus erythematosus;Frontiers in Genetics;2024-03-04

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