Unfazed: parent-of-origin detection for large and small de novo variants
Author:
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
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
Link
http://academic.oup.com/bioinformatics/advance-article-pdf/doi/10.1093/bioinformatics/btab454/40664201/btab454.pdf
Reference11 articles.
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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
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