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NSBDiagnosis Toolkit
A software suite automating the diagnostic steps from Sanger Trace Files (ABIFs) and FASTAs. Namely, this tool is (or will be) capable of:
- Improved consensus conflict resolution via a peak strength metric
- Automatic reporting on variations from a reference file
- Automatic annotating based off pre-existing GenBank data from NCBI
- Automatic pulling GenBank Data
- Automatic querying of Institut Pasteur's MLST databases
- Automatic export of spreadsheet file in the form of a CSV
- User friendly, and automatable (Galaxy compatible) command-line interface
- Interactive Web UI
Description
Takes FASTA sequence and generates output containing multi-locus sequence type and individual alleles.
Languages
Python
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