Article

High-resolution structural variation catalogue in a large-scale whole genome sequenced bovine family cohort data

2022-09-02

Abstract excerpt

<title>Abstract</title> <p>Background Structural variations (SVs) are chromosomal segments that differ between genomes, such as deletions, duplications, insertions, inversions and translocations. The genomics revolution enabled the discovery of sub-microscopic SVs via array and whole-genome sequencing (WGS) data, paving the way to unravel the functional impact of SVs. Recent human expression QTL mapping studies...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: ee655e5e-d7d3-5c38-bd6d-1b7c00f48334
DOI: 10.21203/rs.3.rs-2007387/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

High-resolution structural variation catalogue in a large-scale whole genome sequenced bovine family cohort dataDOI 10.21203/rs.3.rs-2007387/v1Read

High-resolution structural variants catalogue in a large-scale whole genome sequenced bovine family cohort data.Semantic proximity Read

Identification of copy number variations and common deletion polymorphisms in cattle.Semantic proximity Read

A large structural variant collection in Holstein cattle and associated database for variant discovery, characterization, and application.Semantic proximity Read

Assessment of copy number variants in three Brazilian locally adapted cattle breeds using whole-genome re-sequencing data.Semantic proximity Read

Identification of copy number variation in French dairy and beef breeds using next-generation sequencing.Semantic proximity Read

Massive screening of copy number population-scale variation in Bos taurus genome.Semantic proximity Read

Whole genome analysis of breed-specific copy number variations in dogs.Semantic proximity Read

Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array.Semantic proximity Read

Pangenome-based structural variant imputation enables large-scale genotype-phenotype studies in dairy cattle.Semantic proximity Read

Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.Semantic proximity Read

Mapping copy number variable regions correlated with reproduction and production traits in Karan Fries cattle mammalian genomics.Semantic proximity Read

Genomic characteristics of cattle copy number variations.Semantic proximity Read