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CNV analysis using the Affymetrix 6.0 array.
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创建时间：
2011-03-07
相关数据集
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6). Homo sapiens
Systematic evaluation of eleven array platforms commonly used for CNV detection to address parameters of quality and CNV calling. Overall design: 36 Samples
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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.
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.
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GPL10542 - EOHSI-BRTC_Mosquito_11,361_v1
Custom-commercial Aedes aegypti array from Agilent, containing 45220 60-mer probes, designed against the AaegL1.1 set of 16k transcripts at the University of California, Irvine.
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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,
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Additional file 1: Table S1. of Assessing the reproducibility of exome copy number variations predictions
Lists all the IDs used in this study. Table S2 gives details of independent dataset analysis. Tables S3 and S4 give details of size and capture analyses. Table S5 lists ClinSeqÂŽ CNVs identified from
Mendeley Data2024-06-27 更新50
