Single cells Genome Sequencing-1. Homo sapiens

NIAID Data Ecosystem2026-03-07 收录

拷贝数变异

单细胞基因组学

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA178420 数据链接链接失效反馈

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资源简介：

The pilot study on single cell CNV detection in BGI-Shenzhen. Single cells isolated from blood or embryos.

创建时间：

2012-10-29

CNV analysis of iPS cell lines and H2A.X knockout ES cell. Mus musculus

拷贝数变异

干细胞基因组稳定性

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

NIAID Data Ecosystem70

Genomic heterogeneity and clonal evolution in human gastroesophageal junction cancer revealed by single cell DNA sequencing Raw sequence reads

肿瘤克隆进化

单细胞基因组学

This study use single cell DNA sequencing to determine genomic variations and clonal evolution related to lymph node metastasis. Multiple Annealing and Looping Based Amplification Cycles (MALBAC) and

NIAID Data Ecosystem60

All CNVs greater than 2 Mb.

拷贝数变异

基因组结构变异

*Inspection in BeadStudio indicates that this duplication is actually 4.06 Mb, extending from chr2: 106282170�C110339905.**Inspection in BeadStudio indicates that this duplication is actually 2.91 Mb,

Figshare2015-12-02 更新00

A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (GenomeWideSNP_6). Homo sapiens

拷贝数变异

基因芯片平台评估

Systematic evaluation of eleven array platforms commonly used for CNV detection to address parameters of quality and CNV calling. Overall design: 36 Samples

NIAID Data Ecosystem60

HCC1143.dSKY.svg

乳腺癌基因

拷贝数变异

D.SKY plot show the somatic copy number alterations (sCNAs) in cancer cell-line. For this breast cancer cell-line HCC1143, the D.SKY clearly showed the loss of chr8p and gain of chr8q, a pattern recur

DataCite Commons2020-09-04 更新20

Single cells Genome Sequencing-1. Homo sapiens

资源简介：

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