Single nucleotide polymorphism (SNP) has recently become one of the ideal genetic
markers. SNP refers to the DNA sequence polymorphism caused by double nucleotide …

Copy number variations (CNVs) are major forms of genetic variation with an increasing
importance in animal genomics. This study used the Illumina BovineSNP 50 K BeadChip to …

Background Copy number variation (CNV) represents an important source of genetic
divergence that can produce drastic phenotypic differences and may therefore be subject to …

Background Apart from single nucleotide polymorphism (SNP), copy number variation
(CNV) is another important type of genetic variation, which may affect growth traits and play …

Background Copy number variation (CNV) is an important source of genetic variation that
has a significant influence on phenotypic diversity, economically important traits and the …

Copy number variations (CNVs), which cover many functional genes, are associated with
complex diseases, phenotypic diversity and traits that are economically important to raising …

Copy number variation (CNV) is a major proportion of genetic variation, which changes the
gene structure and dosage and affects gene expression and function. To validate the …

Whole-genome sequencing provides a powerful tool to obtain more genetic variability that
could produce a range of benefits for cattle breeding industry. Nanyang (Bos indicus) and …

Current evidences show that copy number variations (CNVs) are linked to complex
phenotypic traits. Leptin receptor (LEPR) gene plays a critical role in energy homeostasis …

Abstract Copy Number Variation (CNV) is the major manner for the variation of genome
structure, which is associated with numerous important traits. The heat shock factor 1 (HSF1) …