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Cryptococcus deneoformans raw sequence reads

NIAID Data Ecosystem2026-03-12 收录

基因组拷贝数变异

隐球菌基因组学

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA716858 数据链接链接失效反馈

官方服务：

资源简介：

Whole genome sequencing of C. deneoformans aneuploid isolates to identify chromosomal copy number variation

应用场景：

创建时间：

2021-03-24

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

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

Copy number variation analysis of human Barrett's esophagus stem cells

基因组拷贝数变异

"Barretts食管研究"

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

NIAID Data Ecosystem50

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