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Denoising DNA deep sequencing data—high-throughput sequencing errors and their correction
Characterizing the errors generated by common high-throughput sequencing platforms and telling true genetic variation from technical artefacts are two interdependent steps, essential to many analyses such as single nucleotide variant calling, haplotype inference, sequence assembly and evolutionary s...
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| Publicado no: | Brief Bioinform |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4719071/ https://ncbi.nlm.nih.gov/pubmed/26026159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbv029 |
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