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BAC CGH array profiling using Phi29-amplified microdissected samples

ChEBI2010-06-05 更新2026-07-21 收录

基因组拷贝数变异

显微切割扩增技术

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-1841 数据链接链接失效反馈

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BAC CGH array profiling using Phi29-amplified microdissected samples

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创建时间：

2010-06-05

基因组拷贝数变异

三倍体遗传诊断

At present, low-pass whole-genome sequencing (WGS) is frequently used in clinical research and in the screening of copy number variations (CNVs). However, there are still some challenges in the detect

NIAID Data Ecosystem120

Tumor T6 Sectors

肿瘤异质性

基因组拷贝数变异

The following CGH experiments were conducted on four sectors (S1-S4) from a single primary ductal carcinoma tumor (T6) using the Sector-Ploidy-Profiling (SPP) Approach. SPP involves macro-dissecting

NIAID Data Ecosystem60

De novo copy number variations in cloned dogs (Illumina SNP)

动物克隆遗传评估

基因组拷贝数变异

De novo copy number variations in cloned dogs (Illumina SNP)

ChEBI2013-12-17 更新50

Table_1_Multivariate piecewise linear regression model to predict radiosensitivity using the association with the genome-wide copy number variation.xlsx

癌症放射敏感性预测

基因组拷贝数变异

IntroductionThe search for biomarkers to predict radiosensitivity is important not only to individualize radiotherapy of cancer patients but also to forecast radiation exposure risks. The aim of this

NIAID Data Ecosystem60

Additional file 4 of Copy number variation of microRNA genes in the human genome

基因组拷贝数变异

microRNA基因定位

Additional file 4:miRNAs located in CNVs with well defined breakpoints. Excel table showing characteristics of miRNAs located in CNVs with well defined breakpoints. (XLS 14 KB)

Figshare2020-08-27 更新50

BAC CGH array profiling using Phi29-amplified microdissected samples

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