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Edge effects in calling variants from targeted amplicon sequencing
BACKGROUND: Analysis of targeted amplicon sequencing data presents some unique challenges in comparison to the analysis of random fragment sequencing data. Whereas reads from randomly fragmented DNA have arbitrary start positions, the reads from amplicon sequencing have fixed start positions that co...
Tallennettuna:
| Julkaisussa: | BMC Genomics |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4302139/ https://ncbi.nlm.nih.gov/pubmed/25480444 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-1073 |
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