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资源简介：
aCGH raw data submitted to Gene Expression Omnibus
应用场景：
创建时间：
2015-01-01
相关数据集
Copy number variation analysis of human Barrett's esophagus stem cells
This SuperSeries is composed of the SubSeries listed below. Refer to individual Series
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Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021529]
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
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Detection rate and false positive rate for microdeletion and microduplication of artificially affected samples.
Detection rate and false positive rate for microdeletion and microduplication of artificially affected samples.
Figshare2017-02-04 更新30
Tumor T18 Sectors
The following CGH experiments were conducted on four sectors (S1-S4) from a single primary ductal carcinoma tumor (T18) using the Sector-Ploidy-Profiling (SPP) Approach. SPP involves macro-dissecting
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TrAEL-seq for CUP1 locus. TrAEL-seq for CUP1 locus
1) The Pgal-3HA cup1 yeast strain, in which all CUP1 ORFs are replaced with 3HA and all CUP1 promoters are replaced by GAL1-10 promoters (PMID: 28654659, which carries ~17 tandem repeats of the modifi
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