2014
DOI: 10.1111/age.12141
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Copy number variation in Fayoumi and Leghorn chickens analyzed using array comparative genomic hybridization

Abstract: Copy number variation refers to regions along chromosomes that harbor a type of structural variation, such as duplications or deletions. Copy number variants (CNVs) play a role in many important traits as well as in genetic diversity. Previous analyses of chickens using array comparative genomic hybridizations or single-nucleotide polymorphism chip assays have been performed on various breeds and genetic lines to discover CNVs. In this study, we assessed individuals from two highly inbred (inbreeding coefficie… Show more

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Cited by 18 publications
(22 citation statements)
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References 65 publications
(185 reference statements)
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“…These unique CNVRs may be recent events in evolution and contribute to breed-specific phenotype and performance [44]. Compared with the eight previous chicken CNV studies [9,[32][33][34]36,[39][40][41], far more CNVRs both on average and in total were found. A total of 6,478 (86.0%) autosomal CNVRs with slightly smaller average size (10.6 kb) were novel, likely due to the higher resolution and sensitivity of NGS method than aCGH and SNP array.…”
Section: Genome-wide Cnv Landscape In the Chicken Genomementioning
confidence: 77%
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“…These unique CNVRs may be recent events in evolution and contribute to breed-specific phenotype and performance [44]. Compared with the eight previous chicken CNV studies [9,[32][33][34]36,[39][40][41], far more CNVRs both on average and in total were found. A total of 6,478 (86.0%) autosomal CNVRs with slightly smaller average size (10.6 kb) were novel, likely due to the higher resolution and sensitivity of NGS method than aCGH and SNP array.…”
Section: Genome-wide Cnv Landscape In the Chicken Genomementioning
confidence: 77%
“…The NGS technology and RD method employed in our work has advantages in both technology platform and genetic diversity compared with the eight previous reports [9,[32][33][34]36,[39][40][41]. Because a significant fraction of CNVs falls into genomic regions not well-covered by microarrays, especially for SD regions lacking sufficient probes [16,23], CNV as a major source of genetic variation is complementary to SNP and could account for a substantial part of missing heritability [14].…”
Section: Discussionmentioning
confidence: 96%
“…; Abernathy et al . ). The smaller gap size of the 600 K SNP array could enable more and shorter CNVs to be detected.…”
Section: Discussionmentioning
confidence: 97%
“…; Abernathy et al . ). Specifically, shared CNVRs had more overlapping proportion than did unique CNVRs, suggesting that these CNVRs may have relatively ancient origins or neutral evolutionary histories and seem to be subsequently introgressed in multiple breeds (Clop et al .…”
Section: Discussionmentioning
confidence: 97%
“…CNVs that have potential roles in economically important traits in chickens have been suggested [58]. Other studies also associated CNVs to diseases [59].…”
Section: Copy Number Variationsmentioning
confidence: 99%