Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins. - Wikidata - awgldk - TriplyDB

Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.

Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.

http://www.wikidata.org/entity/Q36805578

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High density LD-based structural variations analysis in cattle genome Genomic Variants Revealed by Invariably Missing Genotypes in Nelore Cattle Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore Cattle Detection of copy number variations and their effects in Chinese bulls Detection of genome-wide copy number variations in two chicken lines divergently selected for abdominal fat content.Genome-wide detection of copy number variations among diverse horse breeds by array CGH.Genome wide CNV analysis reveals additional variants associated with milk production traits in Holsteins.Genome-wide patterns of copy number variation in the diversified chicken genomes using next-generation sequencing Genomic copy number variation in Mus musculus Genome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds.Genomic population structure and prevalence of copy number variations in South African Nguni cattle.Genome-wide identification of copy number variation using high-density single-nucleotide polymorphism array in Japanese Black cattle.Impact of Parental Bos taurus and Bos indicus Origins on Copy Number Variation in Traditional Chinese Cattle Breeds.Copy number variants in the sheep genome detected using multiple approaches Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.Detection and validation of structural variations in bovine whole-genome sequence data CNV discovery for milk composition traits in dairy cattle using whole genome resequencing.Genome-wide detection of CNVs in Chinese indigenous sheep with different types of tails using ovine high-density 600K SNP arrays Comparative analyses across cattle genders and breeds reveal the pitfalls caused by false positive and lineage-differential copy number variations Enhancing genome-wide copy number variation identification by high density array CGH using diverse resources of pig breeds.Copy Number Variations in Tilapia Genomes.Tropically adapted cattle of Africa: perspectives on potential role of copy number variations.Identification of copy number variations in three Chinese horse breeds using 70K single nucleotide polymorphism BeadChip array.A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.Distribution and Functionality of Copy Number Variation across European Cattle Populations.Genome-Wide SNP Signal Intensity Scanning Revealed Genes Differentiating Cows with Ovarian Pathologies from Healthy Cows.General assessment of copy number variation in normal and tumor tissues of the domestic dog (Canis lupus familiaris).Genome-wide characteristics of copy number variation in Polish Holstein and Polish Red cattle using SNP genotyping assay.Genome-wide association study for milk somatic cell score in holstein cattle using copy number variation as markers.Genome-wide copy number profiling using high-density SNP array in chickens.Detection of breed-specific copy number variations in domestic chicken genome.Genetic Diversity of Seven Cattle Breeds Inferred Using Copy Number Variations.Copy number variation in livestock: A mini review.Misidentification of runs of homozygosity islands in cattle caused by interference with copy number variation or large intermarker distances Identification and Validation of Copy Number Variants in Italian Brown Swiss Dairy Cattle Using Illumina Bovine SNP50 Beadchip®A copy number variant scan in the autochthonous Valdostana Red Pied cattle breed and comparison with specialized dairy populations

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Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.

http://www.wikidata.org/entity/Q36805578

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Haifei Wang

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Jianfeng Liu

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Jicai Jiang

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The diploid genome sequence of an individual human

Towards a comprehensive structural variation map of an individual human genome

Structural variation in the human genome

Gene ontology: tool for the unification of biology

Diversity of human copy number variation and multicopy genes

Mapping copy number variation by population-scale genome sequencing

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Strong synaptic transmission impact by copy number variations in schizophrenia.

Copy number variation at 1q21.1 associated with neuroblastoma

KEGG for representation and analysis of molecular networks involving diseases and drugs

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