GapPredict – A Language Model for Resolving Gaps in Draft Genome Assemblies

Short-read DNA sequencing instruments can yield over 10(12) bases per run, typically composed of reads 150 bases long. Despite this high throughput, de novo assembly algorithms have difficulty reconstructing contiguous genome sequences using short reads due to both repetitive and difficult-to-sequen...

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Detalles Bibliográficos
Autores principales: Chen, Eric, Chu, Justin, Zhang, Jessica, Warren, René L., Birol, Inanc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772386/
https://www.ncbi.nlm.nih.gov/pubmed/34478378
http://dx.doi.org/10.1109/TCBB.2021.3109557

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8772386/
https://www.ncbi.nlm.nih.gov/pubmed/34478378
http://dx.doi.org/10.1109/TCBB.2021.3109557

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