NanoVar Simulation Datasets
收藏NIAID Data Ecosystem2026-03-11 收录
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资源简介：
The data stored here were used for benchmarking long-read structural variant (SV) callers in the publication: Tham, CY., Tirado-Magallanes, R., Goh, Y. et al. NanoVar: accurate characterization of patients’ genomic structural variants using low-depth nanopore sequencing. Genome Biol 21, 56 (2020). https://doi.org/10.1186/s13059-020-01968-7 The data consist of six simulated SV genomes generated using various open source tools and comprise also of simulated long-read FASTA files and ground truth SV information. More information can be found in the README.md.
创建时间：
2020-03-09
