In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and in two commercial breeds (Italian Large White and Italian Duroc) that represent important genetic resources for this species. The genome of 725 pigs was sequenced using a breed-specific DNA pooling approach (30–35 animals per pool) obtaining an average depth per pool of 42×. This approach maximised CNV discovery as well as the related copy number states characterising, on average, the analysed breeds. By mining more than 17.5 billion reads, we identified a total of 9592 CNVs (~683 CNVs per breed) and 3710 CNV regions (CNVRs; 1.15% of the reference pig genome), with an average of 77 CNVRs per breed that were considered as private. A few ...
<div><p>Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
none30siIn this study, we identified copy number variants (CNVs) in 19 European autochthonous pig br...
Abstract In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig ...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
<div><p>Copy number variations (CNVs) are important forms of genomic variation, and have attracted e...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds an...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Abstract Background Copy number variation (CNV) is a major source of structural variants and has bee...
<div><p>Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
none30siIn this study, we identified copy number variants (CNVs) in 19 European autochthonous pig br...
Abstract In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig ...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds and...
<div><p>Copy number variations (CNVs) are important forms of genomic variation, and have attracted e...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
In this study, we identified copy number variants (CNVs) in 19 European autochthonous pig breeds an...
Copy number variations (CNVs) are important forms of genomic variation, and have attracted extensive...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Abstract Background Copy number variation (CNV) is a major source of structural variants and has bee...
<div><p>Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs...
Copy number variations (CNVs) are important forms of genetic variation complementary to SNPs, and ca...
Copy number variations (CNVs) represent a substantial source of structural variants in mammals and c...