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...

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Detalles Bibliográficos
Autores principales: Lee, Hyunji, Kim, Jun, Lee, Junho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
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

Internet

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

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