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资源简介：
Raw sequencing data for SNP and CNV discovery
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创建时间：
2018-07-14
相关数据集
Identification of copy number variations in Jersey cattle using whole genome sequencing and screening deletions for deleterious potential
The following study had two objectives. The first objective was identification of putative CNVs in the US Jersey population using NGS data and validating them by PCR-based assays or other independent
NIAID Data Ecosystem80
Table_2_Population Structure, and Selection Signatures Underlying High-Altitude Adaptation Inferred From Genome-Wide Copy Number Variations in Chinese Indigenous Cattle.xls
Copy number variations (CNVs) have been demonstrated as crucial substrates for evolution, adaptation and breed formation. Chinese indigenous cattle breeds exhibit a broad geographical distribution and
NIAID Data Ecosystem70
Additional file 3 of An IL17RA frameshift variant in a Holstein cattle family with psoriasis-like skin alterations and immunodeficiency
Additional file 3. Twenty-three shared homozygous protein-changing variants in both sequenced cases. The frequency of the corresponding genotypes in the variant catalogue of the 1000 Bulls Genome proj
NIAID Data Ecosystem80
Additional file 2 of Ancestral alleles defined for 70 million cattle variants using a population-based likelihood ratio test
Additional file 2: Method S1. Tools, command lines and thresholds used in processing of raw reads (fastq) to gVCF.
DataCite Commons2024-08-18 更新70
