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资源简介：
a-CGH of Esophageal Cancer (53 cases)
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创建时间：
2014-03-11
相关数据集
Linkage of genetic drivers and strain-specific germline variants confound mouse cancer genome analyses
Cell cultures were isolated from primary pancreatic cancers (PPTs) of KPC mice and subjected to array comparative genomic habridization (aCGH) for the investigation of copy nummber profiles. We genera
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HapMap Yoruban individuals vs CEPH reference
It is becoming clear that copy number polymorphism in the human genome is a significant form of genetic variation. We have developed a new method that uses SNP genotype data from parent-offspring trio
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Array segmentation methods.
Entries in the table indicate the proportion of times (out of 125 observations in each category) that top-down segmentation outperforms the bottom-up approach. Values smaller than (highlighted) indica
Figshare2015-12-02 更新30
Additional file 3 of Copy number variation in human genomes from three major ethno-linguistic groups in Africa
Additional file 3: Table S2. GenomeSTRiP CNVR that intersect cn.MOPS CNVR after QC.
DataCite Commons2020-08-25 更新70
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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