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Tracy: basecalling, alignment, assembly and deconvolution of sanger chromatogram trace files
BACKGROUND: DNA sequencing is at the core of many molecular biology laboratories. Despite its long history, there is a lack of user-friendly Sanger sequencing data analysis tools that can be run interactively as a web application or at large-scale in batch from the command-line. RESULTS: We present...
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| I publikationen: | BMC Genomics |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7071639/ https://ncbi.nlm.nih.gov/pubmed/32171249 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-020-6635-8 |
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