Copy number variation (CNV) might be one of the main contributors to phenotypic diversity and evolutionary adaptation in animals and plants, employing a wide variety of mechanisms, such as gene dosage and transcript structure alterations, to modulate organismal plasticity. In the past 4 years, considerable advances have been made in the characterization of the genomic architecture of CNV in domestic species. First, low-resolution CNV maps were produced for cattle, goat, sheep, pig, dog, chicken, duck and turkey, showing that these structural polymorphisms comprise a significant part of these genomes. Furthermore, CNVs have been associated with several pigmentation (white coat in horse, pig and sheep) and morphological (late feathering and p...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) ...
Copy number variation (CNV) is a phenomenon in which sections of the genome, ranging from one kilo b...
Background Detecting genetic variation is a critical step in elucidating the molecular mechanisms un...
International audienceBACKGROUND: Detecting genetic variation is a critical step in elucidating the ...
<div><p>Copy number variations (CNVs) refer to large insertions, deletions and duplications in the g...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variations (CNVs) refer to large insertions, deletions and duplications in the genomic s...
Copy number variation refers to regions along chromosomes that harbor a type of structural variation...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variation (CNV) is the most prevalent type of genetic structural variation that has been...
Copy number variation (CNV) has been widely used to study the evolution of different species. We fir...
DNA sequence variations include nucleotide substitution, deletion, insertion, translocation and inve...
Background: Detecting genetic variation is a critical step in elucidating the molecular mechanisms u...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) ...
Copy number variation (CNV) is a phenomenon in which sections of the genome, ranging from one kilo b...
Background Detecting genetic variation is a critical step in elucidating the molecular mechanisms un...
International audienceBACKGROUND: Detecting genetic variation is a critical step in elucidating the ...
<div><p>Copy number variations (CNVs) refer to large insertions, deletions and duplications in the g...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variations (CNVs) refer to large insertions, deletions and duplications in the genomic s...
Copy number variation refers to regions along chromosomes that harbor a type of structural variation...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variation (CNV) is the most prevalent type of genetic structural variation that has been...
Copy number variation (CNV) has been widely used to study the evolution of different species. We fir...
DNA sequence variations include nucleotide substitution, deletion, insertion, translocation and inve...
Background: Detecting genetic variation is a critical step in elucidating the molecular mechanisms u...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
Recent studies of mammalian genomes have uncovered the vast extent of copy number variations (CNVs) ...