Copy number variation (CNV) is the most prevalent type of genetic structural variation that has been recognized as an important source of phenotypic variation in humans, animals and plants. However, the mechanisms underlying the evolution of CNVs and their function in natural or artificial selection remain unknown. Here, we generated CNV region (CNVR) datasets which were diverged or shared among cattle, goat, and sheep, including 886 individuals from 171 diverse populations. Using 9 environmental factors for genome-wide association study (GWAS), we identified a series of candidate CNVRs, including genes relating to immunity, tick resistance, multi-drug resistance, and muscle development. The number of CNVRs shared between species is signifi...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
Copy number variation (CNV) represents another important source of genetic variation complementary t...
Copy number variation (CNV) is the most prevalent type of genetic structural variation that has been...
Copy number variation (CNV) is a phenomenon in which sections of the genome, ranging from one kilo b...
Goats (Capra hircus) are an important farm animal species. Copy number variation (CNV) represents a ...
Background: Copy number variation (CNV) represents another important source of genetic variation com...
Copy number variation (CNV) might be one of the main contributors to phenotypic diversity and evolut...
Copy number variants (CNV) are insertions or deletions of 1 kb or larger in a genome with variable n...
Copy number variation (CNV) is a major source of genomic structural variation. The aim of this study...
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) ...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
Copy number variation (CNV) represents another important source of genetic variation complementary t...
Copy number variation (CNV) is the most prevalent type of genetic structural variation that has been...
Copy number variation (CNV) is a phenomenon in which sections of the genome, ranging from one kilo b...
Goats (Capra hircus) are an important farm animal species. Copy number variation (CNV) represents a ...
Background: Copy number variation (CNV) represents another important source of genetic variation com...
Copy number variation (CNV) might be one of the main contributors to phenotypic diversity and evolut...
Copy number variants (CNV) are insertions or deletions of 1 kb or larger in a genome with variable n...
Copy number variation (CNV) is a major source of genomic structural variation. The aim of this study...
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) ...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
<p>Copy number variations (CNVs) comprise deletions, duplications, and insertions found within the g...
Copy number variation (CNV) represents another important source of genetic variation complementary t...