Versatile Identification of Copy Number Variants with Canvas
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-8666-8_12
Reference15 articles.
1. Navin NE (2010) Tracing the tumor lineage. Mol Oncol 4:267–283
2. Acuna-Hidalgo R et al (2016) New insights into the generation and role of de novo mutations in health and disease. Genome Biol 17:241
3. Teo SM et al (2012) Statistical challenges associated with detecting copy number variations with next-generation sequencing. Bioinformatics 28:2711–2718
4. Abyzov A et al (2011) CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res 21:974–984
5. Boeva V et al (2011) Control-FREEC: a tool for assessing copy number and allelic content using next generation sequencing data. Bioinformatics 28:423–425
Cited by 2 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. Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma;British Journal of Cancer;2024-07-12
2. The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer;British Journal of Cancer;2022-04-22
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