2021
DOI: 10.1080/10495398.2021.1942027
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Genome-wide detection of copy number variations in Tharparkar cattle

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Cited by 30 publications
(11 citation statements)
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“…Structural variants in the genome, such as insertions and deletions, as well as copy number variations (CNVs) and chromosomal rearrangements such as duplications, inversions, and translocations (Tattini et al, 2015), are targeted during selection events for traits related to morphology, production, and reproduction. Copy number variations are a significant source of genetic variation that aid in understanding prevalent phenotypic diversity, economic traits, and livestock species evolution (Kumar et al, 2021). Yuan et al (2021) used whole-genome resequencing to study CNVs in Chinese indigenous fine-wool sheep populations.…”
Section: Sheepmentioning
confidence: 99%
“…Structural variants in the genome, such as insertions and deletions, as well as copy number variations (CNVs) and chromosomal rearrangements such as duplications, inversions, and translocations (Tattini et al, 2015), are targeted during selection events for traits related to morphology, production, and reproduction. Copy number variations are a significant source of genetic variation that aid in understanding prevalent phenotypic diversity, economic traits, and livestock species evolution (Kumar et al, 2021). Yuan et al (2021) used whole-genome resequencing to study CNVs in Chinese indigenous fine-wool sheep populations.…”
Section: Sheepmentioning
confidence: 99%
“…Genetic variation lurked multifarious historical events, reflecting the historical selection and evolutionary pressures experienced as various cattle breeds developed ( Ahmad et al, 2020 ; Kumar et al, 2021a ; Kumar et al, 2021b ; Ghildiyal et al, 2023 ). ROH is a critical metric for evaluating inbreeding and recessive inheritance ( Curik et al, 2014 ; Nandolo et al, 2018 ).…”
Section: Discussionmentioning
confidence: 99%
“…We chose the CNV method by region approach for our investigation. Subsequently, we applied a recurrence value of 0.3, as advised by the CNVRuler manual and previous studies [ 25 ], to avoid overestimating the size and frequency of CNVRs. Finally, control raw data filtered for occurrence in at least three individuals were used as the last of our results.…”
Section: Methodsmentioning
confidence: 99%