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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Bibliographic Details
Main Authors: Peng Lu, Jingjing Jin, Zefeng Li, Yalong Xu, Dasha Hu, Jiajun Liu, Peijian Cao
Format: Article
Language:English
Published: SAGE Publishing 2020-04-01
Series:Evolutionary Bioinformatics
Online Access:https://doi.org/10.1177/1176934320913859

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