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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...
Shranjeno v:
| izdano v: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2019
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| Teme: | |
| Online dostop: | 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 |
| Oznake: |
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