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Benchmarking datasets for assembly-based variant calling using high-fidelity long reads
BACKGROUND: Recent advances in long-read sequencing technologies have enabled accurate identification of all genetic variants in individuals or cells; this procedure is known as variant calling. However, benchmarking studies on variant calling using different long-read sequencing technologies are st...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045170/ https://www.ncbi.nlm.nih.gov/pubmed/36973656 http://dx.doi.org/10.1186/s12864-023-09255-y |