sabre

Browse sequence alignments.

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mismatch ambiguous consensus leading/trailing gap

            
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How to use sabre
  1. Paste a FASTA alignment or upload a FASTA/FASTA.gz file.
  2. Adjust “Characters per line” to control alignment wrapping.
  3. Click Launch Analysis to render the alignment.
  4. Use Load Example to try a bundled demo dataset.
Tips
  • Only DNA alignments are supported at the moment.
  • Hover over characters to see alignment/sequence positions and metadata.
  • The legend highlights mismatches, ambiguous consensus calls, and end gaps.