首页/数据集/DNA copy number gain at 1q23.3 is associated with poor survival in metastatic bladder cancer [Agilent]

DNA copy number gain at 1q23.3 is associated with poor survival in metastatic bladder cancer [Agilent]

ChEBI2013-07-07 更新2026-07-21 收录

膀胱癌基因组学

拷贝数变异

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-39281 数据链接链接失效反馈

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DNA copy number gain at 1q23.3 is associated with poor survival in metastatic bladder cancer [Agilent]

应用场景：

创建时间：

2013-07-07

基因重复分析

拷贝数变异

VMR for genes with different duplication states. Shown is the average VMR for the whole genome, unique genes, segmental duplicated genes and tandem duplicated genes.

NIAID Data Ecosystem90

Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [Agilent021365]. Homo sapiens

拷贝数变异

微阵列平台

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

NIAID Data Ecosystem70

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

Molecular karyotyping

拷贝数变异

药物诱导基因组不稳定性

CNVs detected in MMC-treated and untreated cells using molecular karyotyping. Raw data

NIAID Data Ecosystem70

Additional file 8: Table S6. of Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases

神经干细胞

拷贝数变异

De novo copy number variations (CNVs) identified in the 1201C1 iPSC-derived NSPCs. (XLSX 35Â kb)

DataCite Commons2024-12-17 更新70