Evaluation of the impact of Illumina error correction tools on de novo genome assembly
Abstract Background Recently, many standalone applications have been proposed to correct sequencing errors in Illumina data. The key idea is that downstream analysis tools such as de novo genome assemblers benefit from a reduced error rate in the input data. Surprisingly, a systematic validation of...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2017-08-01
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| Σειρά: | BMC Bioinformatics |
| Θέματα: | |
| Διαθέσιμο Online: | http://link.springer.com/article/10.1186/s12859-017-1784-8 |
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