NGmerge: merging paired-end reads via novel empirically-derived models of sequencing errors
Abstract Background Advances in Illumina DNA sequencing technology have produced longer paired-end reads that increasingly have sequence overlaps. These reads can be merged into a single read that spans the full length of the original DNA fragment, allowing for error correction and accurate determin...
Kaydedildi:
| Yazar: | |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2018-12-01
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| Seri Bilgileri: | BMC Bioinformatics |
| Konular: | |
| Online Erişim: | http://link.springer.com/article/10.1186/s12859-018-2579-2 |
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