PGcloser: Fast Parallel Gap-Closing Tool Using Long-Reads or Contigs to Fill Gaps in Genomes

Assembled draft genomes usually contain many gaps because of the length limit of next-generation sequencing. Although many gap-closing tools have been developed, most of them still attempt to fill gaps on the basis of next-generation sequencing reads (always < 200 bp). Hence, the gap-filling effe...

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Detalles Bibliográficos
Autores principales: Lu, Peng, Jin, Jingjing, Li, Zefeng, Xu, Yalong, Hu, Dasha, Liu, Jiajun, Cao, Peijian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Parallel Computing in Evolutionary Bioinformatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180314/
https://www.ncbi.nlm.nih.gov/pubmed/32362739
http://dx.doi.org/10.1177/1176934320913859

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180314/
https://www.ncbi.nlm.nih.gov/pubmed/32362739
http://dx.doi.org/10.1177/1176934320913859

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