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SubclonalHeterogeneity_SomaticSniper-Battenberg_CNVs - samples

NIAID Data Ecosystem2026-03-11 收录

肿瘤亚克隆异质性分析

拷贝数变异

数据链接：

https://www.omicsdi.org/dataset/ega/EGAD00001004405 数据链接链接失效反馈

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资源简介：

CNA calls generated using the SomaticSniper-Battenberg-PhyloWGS from the CPC-GENE Subclonal Heterogeneity studyEGA dataset EGAD00001004405

应用场景：

创建时间：

2019-04-25

病毒基因分析

拷贝数变异

Table S1. Each row reports the results of analyses of single nucleotide variation in the indicated gene. The first and second columns report nucleotide diversity (π) within the AZ and TX/MX/SA populat

Mendeley Data2024-06-27 更新90

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

Additional file 3 of A genome-wide scan of copy number variants in three Iranian indigenous river buffaloes

基因组学

拷贝数变异

Additional file 3: Supplementary Table S3 List of 203 non redundant CNVRs. Samples count for each breed, genes and QTL are also reported.

DataCite Commons2021-04-27 更新60

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

SubclonalHeterogeneity_SomaticSniper-Battenberg_CNVs - samples

资源简介：

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