首页/数据集/Validation of a subset of copy number variants from GSE24424 by aCGH

Validation of a subset of copy number variants from GSE24424 by aCGH

ChEBI2010-12-31 更新2026-07-21 收录

拷贝数变异

阵列比较基因组杂交

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-24640 数据链接链接失效反馈

官方服务：

资源简介：

Validation of a subset of copy number variants from GSE24424 by aCGH

应用场景：

创建时间：

2010-12-31

癌症基因组数据

拷贝数变异

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

NIAID Data Ecosystem80

HapMap Yoruban individuals vs CEPH reference

拷贝数变异

遗传多态性

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

NIAID Data Ecosystem70

Array segmentation methods.

拷贝数变异

阵列分割算法

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

基因组学

拷贝数变异

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

甲状腺功能异常

拷贝数变异

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,

NIAID Data Ecosystem60

Validation of a subset of copy number variants from GSE24424 by aCGH

资源简介：

相关数据集