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GAPPadder: a sensitive approach for closing gaps on draft genomes with short sequence reads

BACKGROUND: Closing gaps in draft genomes is an important post processing step in genome assembly. It leads to more complete genomes, which benefits downstream genome analysis such as annotation and genotyping. Several tools have been developed for gap closing. However, these tools don’t fully utili...

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Foilsithe in:BMC Genomics
Main Authors: Chu, Chong, Li, Xin, Wu, Yufeng
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2019
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6551238/
https://ncbi.nlm.nih.gov/pubmed/31167639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-019-5703-4
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