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...
| Hlavní autoři: | , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
PeerJ Inc.
2022-10-01
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| Edice: | PeerJ |
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| On-line přístup: | https://peerj.com/articles/14186.pdf |