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RFfiller: a robust and fast statistical algorithm for gap filling in draft genomes
Numerous published genomes contain gaps or unknown sequences. Gap filling is a critical final step in de novo genome assembly, particularly for large genomes. While certain computational approaches partially address the problem, others have shortcomings regarding the draft genome’s dependability and...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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PeerJ Inc.
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575681/ https://www.ncbi.nlm.nih.gov/pubmed/36262414 http://dx.doi.org/10.7717/peerj.14186 |