NanoVar: accurate characterization of patients’ genomic structural variants using low-depth nanopore sequencing

The recent advent of third-generation sequencing technologies brings promise for better characterization of genomic structural variants by virtue of having longer reads. However, long-read applications are still constrained by their high sequencing error rates and low sequencing throughput. Here, we...

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Detalles Bibliográficos
Autores principales: Tham, Cheng Yong, Tirado-Magallanes, Roberto, Goh, Yufen, Fullwood, Melissa J., Koh, Bryan T.H., Wang, Wilson, Ng, Chin Hin, Chng, Wee Joo, Thiery, Alexandre, Tenen, Daniel G., Benoukraf, Touati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055087/
https://www.ncbi.nlm.nih.gov/pubmed/32127024
http://dx.doi.org/10.1186/s13059-020-01968-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055087/
https://www.ncbi.nlm.nih.gov/pubmed/32127024
http://dx.doi.org/10.1186/s13059-020-01968-7

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