A snapshot of CNVs in the pig genome.
Recent studies of mammalian genomes have uncovered the extent of copy number variation (CNV) that contributes to phenotypic diversity, including health and disease status. Here we report a first account of CNVs in the pig genome covering part of the chromosomes 4, 7, 14, and 17 already sequenced and...
Enregistré dans:
Auteurs principaux: | João Fadista, Marianne Nygaard, Lars-Erik Holm, Bo Thomsen, Christian Bendixen |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Public Library of Science (PLoS)
2008
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/f409d31e4b6c42dbab715f8701dcd1ed |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Accurate distinction of pathogenic from benign CNVs in mental retardation.
par: Jayne Y Hehir-Kwa, et autres
Publié: (2010) -
A genomic snapshot of Salmonella enterica serovar Typhi in Colombia.
par: Paula Diaz Guevara, et autres
Publié: (2021) -
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.
par: Danielle P Moreira, et autres
Publié: (2014) -
A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer
par: Yajun Yu, et autres
Publié: (2021) -
Snapshot of the eukaryotic gene expression in muskoxen rumen--a metatranscriptomic approach.
par: Meng Qi, et autres
Publié: (2011)