Pangenomics enables genotyping of known structural variants in 5202 diverse genomes
Author(s) -
Jouni Sirén,
Jean Monlong,
Xian Chang,
Adam M. Novak,
Jordan M. Eizenga,
Charles Markello,
Jonas A. Sibbesen,
Glenn Hickey,
Pi-Chuan Chang,
Andrew Carroll,
Namrata Gupta,
Stacey Gabriel,
Thomas W. Blackwell,
Aakrosh Ratan,
Kent D. Taylor,
Stephen S. Rich,
Jerome I. Rotter,
David Haussler,
Erik Garrison,
Benedict Paten
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abg8871
Subject(s) - genotyping , genome , reference genome , structural variation , biology , computational biology , haplotype , human genome , genetics , genotype , gene
Giraffe pangenomes Genomes within a species often have a core, conserved component, as well as a variable set of genetic material among individuals or populations that is referred to as a “pangenome.” Inference of the relationships between pangenomes sequenced with short-read technology is often done computationally by mapping the sequences to a reference genome. The computational method affects genome assembly and comparisons, especially in cases of structural variants that are longer than an average sequenced region, for highly polymorphic loci, and for cross-species analyses. Sirenet al . present a bioinformatic method called Giraffe, which improves mapping pangenomes in polymorphic regions of the genome containing single nucleotide polymorphisms and structural variants with standard computational resources, making large-scale genomic analyses more accessible. —LMZ
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