Profiling of copy-number variation between BN and M520 rats

Alliance of Genome Resources2026-08-01 收录

拷贝数变异

大鼠品系比较基因组

数据链接：

https://www.ncbi.nlm.nih.gov/gds/?term=GSE27368 数据链接链接失效反馈

官方服务：

资源简介：

We used Nimblegen HD aCGH to detect copy-number variants between genomes of BN and M520 rats

High-resolution profiling of copy-number aberrations in osteosarcoma

骨肉瘤

拷贝数变异

Osteosarcoma is a rare, highly malignant tumor of the bone that presents with a highly complex and abnormal karyotype. Only a few of the genes, which are targets of genetic alteration are known. An in

NIAID Data Ecosystem70

Additional file 8 of Genome-wide characterization of copy number variations in the host genome in genetic resistance to Marek’s disease using next generation sequencing

基因组学

拷贝数变异

Additional file 8: Table S7. The detailed information of CNVRs identified in this study and previous studies.

DataCite Commons2024-02-08 更新40

Noninvasive prenatal detection for pathogenic CNVs related with fetal monogenetic diseases

遗传病筛查

拷贝数变异

Noninvasive prenatal detection for pathogenic CNVs related with fetal monogenetic diseases using target region capture sequencing.

DataCite Commons2020-10-10 更新30

Detection of copy number variation in patients with Pelizaeus-Merzbacher disease (PMD) - NimbleGen

Pelizaeus-Merzbacher病遗传学

拷贝数变异

The objective of the study was to investigate the extent of duplicated, triplicated, and quadruplicated regions in PMD patients so that junction analysis could be performed. 10 samples were analyzed.

NIAID Data Ecosystem40

A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants (WGTP)

拷贝数变异

基因组微阵列评估

Systematic evaluation of eleven array platforms commonly used for CNV detection to address parameters of quality and CNV calling. 18 Samples

NIAID Data Ecosystem40