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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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| Udgivet i: | BMC Genomics |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2019
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| Fag: | |
| Online adgang: | 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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