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CNVs identified for each family.
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创建时间:
2016-10-12
相关数据集
Supplementary Material for: Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects
Array comparative genomic hybridization (aCGH) has led to an increased detection of causal chromosomal imbalances in individuals with congenital heart defects (CHD). The introduction of aCGH as a diag
DataCite Commons2020-09-02 更新120
Additional file 8 of Identification and population genetic analyses of copy number variations in six domestic goat breeds and Bezoar ibexes using next-generation sequencing
Additional file 8: Table S6. Significantly enriched terms for the differentiation CNV genes identified in this study.
DataCite Commons2024-02-13 更新60
Additional file 1 of Detection of copy number variants in African goats using whole genome sequence data
Additional file 1 Supplementary Table 1 Genes in CNV with VST values above the 99th percentile for each comparison. Supplementary Table 2 List of CNVR by population. Supplementary Table 3 Summary of C
DataCite Commons2024-02-06 更新50
CNVRs Identified in Afghan Arabian Sheep Breeds.csv
The CNVRs identified in Afghan sheep breeds: The aim of this study was to identify CNVs in 45 Afghan sheep consisting of three Arab, Baluchi, and Gedic breeds using genomic arrays containing 53862 sin
DataCite Commons2022-08-03 更新70
Table_1_Pan-Genomic Study of Mycobacterium tuberculosis Reflecting the Primary/Secondary Genes, Generality/Individuality, and the Interconversion Through Copy Number Variations.DOCX
Tuberculosis (TB) has surpassed HIV as the leading infectious disease killer worldwide since 2014. The main pathogen, Mycobacterium tuberculosis (Mtb), contains ~4,000 genes that account for ~90% of t
NIAID Data Ecosystem50



