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Gencore: an efficient tool to generate consensus reads for error suppressing and duplicate removing of NGS data
BACKGROUND: Removing duplicates might be considered as a well-resolved problem in next-generation sequencing (NGS) data processing domain. However, as NGS technology gains more recognition in clinical application, researchers start to pay more attention to its sequencing errors, and prefer to remove...
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| Udgivet i: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6933617/ https://ncbi.nlm.nih.gov/pubmed/31881822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-3280-9 |
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