NanoVar Simulation Datasets
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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. <em>et al.</em> NanoVar: accurate characterization of patients’ genomic structural variants using low-depth nanopore sequencing. <em>Genome Biol</em> <strong>21, </strong>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.
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Zenodo创建时间：
2019-12-28
