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Mate pair whole genome sequencing in leukemia

NIAID Data Ecosystem2026-03-10 收录

白血病基因组

结构变异检测

数据链接：

https://www.ncbi.nlm.nih.gov/bioproject/PRJNA415732 数据链接链接失效反馈

官方服务：

资源简介：

We have investigated the suitability of MP-WGS to detect structural rearrangements in leukemia samples in the diagnostic setting

应用场景：

创建时间：

2017-10-25

结构变异检测

基因组参考评估

To compare and contrast the necessity to explore mapping long-read genome sequencing data to the recently published Telomere-to-Telomere (T2T) reference genome for detection of rare and pathogenic inv

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Mapping and phasing of structural variation in patient genomes using nanopore sequencing

结构变异检测

基因型分组

We whole genome sequence 2 patients with congenital abnormalities and known complex de novo chromosomal rearrangements using the Nanopore MinION. We show how we can detect most previoulsy detected de

NIAID Data Ecosystem50

Long-read sequencing data from cattle for the purpose of de-novo genome assembly. Long-read sequencing of cattle

基因组组装

结构变异检测

A collection of whole-genome long-read sequencing data from individuals representing different breeds of cattle. These data are used to create reference-quality assemblies and derive structural variat

NIAID Data Ecosystem30

Chromothripsis is a frequent event and underlies typical genetic changes in early T-cell precursor lymphoblastic leukemia in adults

白血病基因组

染色体碎裂分析

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

NIAID Data Ecosystem50

COLO829 SV benchmark (v2)

结构变异检测

基因组基准测试

Files used to create a new Structural Variant (SV) benchmark colo the cell line COLO829 in reference genome coordinates GRCh38 and CHM13-T2T

Zenodo2024-01-01 更新40