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

1-to-1 comparison of CNA between Illumina targeted NGS and SNP arrays

基因组学

拷贝数变异

Supplementary Data S2: Segmented Log2 ratios for the Illumina TGS Supplementary Data S3: Segmented Log2 ratios for the Affymetrix OncoScan FFPE Express SNP arrays Note: All data are d

DataCite Commons2020-09-02 更新40

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

Additional file 9 of MetaCNV - a consensus approach to infer accurate copy numbers from low coverage data

基因组学

拷贝数变异

Additional file 9. CNVcalling SKBR3–3 cells CNV calling results for SKBR3–3 cells.

DataCite Commons2020-08-25 更新50