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<p>Structural variants identified using Nanopore long-read data.</p>

NIAID Data Ecosystem2026-05-10 收录

数据链接：

https://figshare.com/articles/dataset/_p_Structural_variants_identified_using_Nanopore_long-read_data_p_/30915886 数据链接链接失效反馈

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资源简介：

Structural variants identified using Nanopore long-read data.

应用场景：

创建时间：

2025-12-18

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

NIAID Data Ecosystem60

Raw Fast5 data for "Microbiota profiling with long amplicons using Nanopore sequencing: full-length 16S rRNA gene and the 16S-ITS-23S of the rrn operon" - PART I

微生物组

Nanopore长读长测序

Raw Fast5 data for "Microbiota profiling with long amplicons using Nanopore sequencing: full-length 16S rRNA gene and the 16S-ITS-23S of the rrn operon". See Supplementary Table 2 for associating each

NIAID Data Ecosystem40

Additional file 16 of Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies

癌症基因组数据

结构变异检测

Additional file 16: Supplementary Table S15. Summary of BND events characterized by multiple software tools from PacBio, ONT, HiC, Illumina, 10X and Bionano data sets.

Figshare2024-08-13 更新30

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

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