PROBE DATA - ALL SAMPLES

Dryad2019-01-01 更新2026-04-13 收录

拷贝数变异

SNP阵列探针分析

数据链接：

https://datadryad.org/resource/doi:10.5061/dryad.314k5k5/2 数据链接链接失效反馈

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资源简介：

Data output from SNP Array analyses in Nexus Copy Number v7.5 (BioDiscovery, Inc.). Probe data per chromosome for all samples

创建时间：

2019-01-01

Additional file 2 of Comprehensive characterization of copy number variation (CNV) called from array, long- and short-read data

基因组学

拷贝数变异

Additional file 2 CNVR and associated CNV loci. CNVR and associated CNV loci coordinates and scores for the four quality bins, based on long-read score (all, score >1, score >5) and long-read an

DataCite Commons2021-11-18 更新70

Post-filter CNV counts and relative CNV frequency.

拷贝数变异

基因组数据质量控制

The CNV counts shown here represent the 43,560 candidate CNVs that remain after applying the Post-filter. The first column shows a specific CNV count. The second set of columns show the number of cont

NIAID Data Ecosystem60

VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.

基因重复分析

拷贝数变异

VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.

NIAID Data Ecosystem60

A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6). Homo sapiens

拷贝数变异

基因芯片平台评估

Systematic evaluation of eleven array platforms commonly used for CNV detection to address parameters of quality and CNV calling. Overall design: 36 Samples

NIAID Data Ecosystem60

Somatic CNV profile of congenital ectopic thyroids

甲状腺功能异常

拷贝数变异

To assess whether specific genes have relevant somatic genetic or epigenetic alterations in ectopic tissue, we used a combined analysis of transcriptome (confirmed by qRT-PCR on 68 genes), methylome,

NIAID Data Ecosystem60

PROBE DATA - ALL SAMPLES

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