Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.

Genetics and molecular research : GMR - 2 Oct 2015

Salomón-Torres R, González-Vizcarra V M, Medina-Basulto G E, Montaño-Gómez M F, Mahadevan P, Yaurima-Basaldúa V H, Villa-Angulo C, Villa-Angulo R

Abstract excerpt

Copy number variations (CNVs) are an important source of genomic structural variation, and can be used as markers to investigate phenotypic and economic traits. CNVs also have functional effects on gene expression and can contribute to disease susceptibility in mammals. Currently, single nucleotide polymorphism genotyping arrays (SNP chips) are the technology of choice for identifying CNV variations. Microarray...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to Dairying

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Genome

Share to Genotyping Techniques

Share to Mexico

Share to Oligonucleotide Array Sequence Analysis

Share to Quantitative Trait, Heritable

Source

Identifiers

PMID: 26436509
DOI: 10.4238/2015.October.2.18

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.PMID 26436509Read ↗

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

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

High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data.Semantic proximity Read ↗

Genomic characteristics of cattle copy number variations.Semantic proximity Read ↗

Identification of copy number variations in Qinchuan cattle using BovineHD Genotyping Beadchip array.Semantic proximity Read ↗

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

A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.Semantic proximity Read ↗

Copy number variant scan in more than four thousand Holstein cows bred in Lombardy, Italy.Semantic proximity Read ↗

Characterization of copy number variants in a large multibreed population of beef and dairy cattle using high-density single nucleotide polymorphism genotype data1Semantic proximity Read ↗

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

Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs.Semantic proximity Read ↗

Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.