Detection of copy number variations in brown and white layers based on genotyping panels with different densities.

ABSTRACT:

Background

Copy number variations (CNV) are an important source of genetic variation that has gained increasing attention over the last couple of years. In this study, we performed CNV detection and functional analysis for 18,719 individuals from four pure lines and one commercial cross of layer chickens. Samples were genotyped on four single nucleotide polymorphism (SNP) genotyping platforms, i.e. the Illumina 42K, Affymetrix 600K, and two different customized Affymetrix 50K chips. CNV recovered from the Affymetrix chips were identified by using the Axiom^® CNV Summary Tools and PennCNV software and those from the Illumina chip were identified by using the cnvPartition in the Genome Studio software.

Results

The mean number of CNV per individual varied from 0.50 to

SUBMITTER: Drobik-Czwarno W 

PROVIDER: S-EPMC6219011 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature