HAT: haplotype assembly tool using short and error-prone long reads

MOTIVATION: Haplotypes are the set of alleles co-occurring on a single chromosome and inherited together to the next generation. Because a monoploid reference genome loses this co-occurrence information, it has limited use in associating phenotypes with allelic combinations of genotypes. Therefore,...

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Detalles Bibliográficos
Autores principales: Shirali Hossein Zade, Ramin, Urhan, Aysun, Assis de Souza, Alvaro, Singh, Akash, Abeel, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750119/
https://www.ncbi.nlm.nih.gov/pubmed/36308461
http://dx.doi.org/10.1093/bioinformatics/btac702

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9750119/
https://www.ncbi.nlm.nih.gov/pubmed/36308461
http://dx.doi.org/10.1093/bioinformatics/btac702

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