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Repeat-aware modeling and correction of short read errors
BACKGROUND: High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome...
Tallennettuna:
| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3044310/ https://ncbi.nlm.nih.gov/pubmed/21342585 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-S1-S52 |
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