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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.
Readme 2.1 MiB
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Python 100%