Unfazed: parent-of-origin detection for large and small de novo variants

Author:

Belyeu Jonathan R12ORCID,Sasani Thomas A123,Pedersen Brent S12ORCID,Quinlan Aaron R12ORCID

Affiliation:

1. Department of Human Genetics, Salt Lake City, UT 84112, USA

2. Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT 84112, USA

3. Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA

Abstract

Abstract Summary Unfazed is a command-line tool to determine the parental gamete of origin for de novo mutations from paired-end Illumina DNA sequencing reads. Unfazed uses variant information for a sequenced trio to identify the parental gamete of origin by linking phase-informative inherited variants to de novo mutations using read-based phasing. It achieves a high success rate by chaining reads into haplotype groups, thus increasing the search space for informative sites. Unfazed provides a simple command-line interface and scales well to large inputs, determining parent-of-origin for nearly 30 000 de novo variants in under 60 h. Availability and implementation Unfazed is available at https://github.com/jbelyeu/unfazed. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

US National Human Genomic Research Institute

US National Institute of General Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference11 articles.

1. De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families;Belyeu;Am. J. Hum. Genet.,2020

2. Samplot: a platform for structural variant visual validation and automated filtering;Belyeu;Genome Biol.,2020

3. Rare variant phasing and haplotypic expression from RNA sequencing with phASER;Castel;Nat. Commun,2016

4. Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications;Chen;Bioinformatics,2016

5. Center d’Etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome;Dausset;Genomics,1990

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