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CGH data from 58 bladder tumors
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2010-05-19
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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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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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Table S3 : Consistently divergent CNVs in the Control Test from The role of copy-number variation in the reinforcement of sexual isolation between the two European subspecies of the house mouse
this file is in .txt format
DataCite Commons2020-08-25 更新40
Post-filter CNV counts and relative CNV frequency.
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
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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
