SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference19 articles.
1. Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families;D Ford;American Journal of Human Genetics,1998
2. Large genomic deletions inactivate the BRCA2 gene in breast cancer families;S Agata;J Med Genet,2005
3. Large Genomic Deletions and Duplications in the BRCA1 Gene Identified by a Novel Quantitative;FBL Hogervorst;Methods - Cancer Research,2003
4. Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families;M Montagna;Hum Mol Genet,2003
5. The Relative Contribution of Point Mutations and Genomic Rearrangements in BRCA1 and BRCA2 in High-Risk Breast Cancer Families;MD Palma;Cancer Res,2008
Cited by 33 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. Detecting gene breakpoints in noisy genome sequences using position-annotated colored de-Bruijn graphs;BMC Bioinformatics;2023-06-05
2. Overview of structural variation calling: Simulation, identification, and visualization;Computers in Biology and Medicine;2022-06
3. Exon skipping caused by a complex structural variation in SH2D1A resulted in X‐linked lymphoproliferative syndrome type 1;Molecular Genetics & Genomic Medicine;2022-01-29
4. Loose ends in cancer genome structure;2021-05-27
5. DINTD: Detection and Inference of Tandem Duplications From Short Sequencing Reads;Frontiers in Genetics;2020-08-11
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