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Array CGH in congenital heart disease
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创建时间：
2008-05-11
相关数据集
Supplementary Tables: Genome organization and copy-number variation reveal clues to virulence evolution in Coccidioides posadasii
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
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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CNV analysis of iPS cell lines and H2A.X knockout ES cell. Mus musculus
It is well-known that embryonic stem cells (ESC) are much more sensitive to replication-induced stress than differentiated cells but the underpinning mechanisms are largely unknown. H2A.X, a minor var
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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
NIAID Data Ecosystem60
