官方服务：
资源简介：
CNAs detection in plasma and tissue for each patient.
应用场景：
创建时间：
2021-02-04
相关数据集
Molecular karyotyping
CNVs detected in MMC-treated and untreated cells using molecular karyotyping. Raw data
NIAID Data Ecosystem70
Somatic CNV profile of congenital ectopic thyroids
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
Preanalytical Impacts on Copy Number Variation Detection by aCGH Technology. Preanalytical Impacts on Copy Number Variation Detection by aCGH Technology
The Biospecimen Pre-analytical Variables (BPV) Program is a National Cancer Institute-sponsored study to systematically assess the effects of pre-analytical factors on the molecular profile of biospec
NIAID Data Ecosystem40
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]. Homo sapiens
Background: High-resolution microarray technology is routinely used in basic research and clinical practice to efficiently detect copy number variants (CNVs) across the entire human genome. A new gene
NIAID Data Ecosystem70
Variance stable normalisation for Illumina targeted NGS
Raw Log2 ratios output of CNVkit. Three datasets are provided. Each one contains the full set of samples normalised against one of three clusters of normal samples identified using a model based clust
NIAID Data Ecosystem40
