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Biological Sequence & Alignment Viewer

ChatGPT plugin

Inspect, analyze, and compare biological sequences and alignments.

View in ChatGPT directory

Biological Sequence & Alignment Viewer helps you inspect, analyze, safely edit, and compare FASTA, GenBank, EMBL, FASTQ, multiple sequence alignments, Sanger ABIF/SCF traces, and supported SnapGene DNA files. Navigate linear or circular records, manage annotations, translate with the right genetic code, find ORFs, explore primers and restriction digests, inspect measured chromatogram signals, align or edit copies, build graphical guide trees, load mapped variant/read evidence, export reproducible artifacts, restore sessions, and ask follow-up questions grounded in authoritative live viewer state. Unsupported binary revisions and source metadata are reported explicitly.

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Rank by placement

#2311of 8,79336places up24h171places up7d
#2,234#2,465#2,696#2,927#3,158Sep 27Oct 3Oct 9Oct 15Oct 21Oct 26

Rank in Scientific research

#13of 34024h07d
#12#13Sep 27Oct 3Oct 9Oct 15Oct 21Oct 26

8 listing changes logged · latest Oct 25: Version, One-liner. See what changed

In its category

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Scientific research13th of 34 by placement
#PluginPosition7d
11Molecular Structure Viewer#1857208places up
12Boltz#200067places down
13Biological Sequence & Alignment ViewerThis page#2311171places up
14Biohub ESM#2807148places up
15Slide Viewer#293040places up

All 34 Scientific research plugins

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Example prompts

  • “Fetch ENA DRR037765 first 500 reads to active workspace; open and report live length range, GC, Q30, and subset provenance”
  • “Fetch UniProt P01116/P01111/P01112 alignment; map conserved motifs to KRAS, compute distances/tree, publish Newick to workspace”
  • “Fetch NCBI NC_001416.1 to active workspace; open it, map cI to OR1–OR3, and translate cI with code 11”

Skills

  • biological-sequence-viewer

    Open, inspect, analyze, safely edit copies of, and export local biological sequences and alignments in Codex's interactive workbench. Use for FASTA/FASTQ, GenBank/EMBL, MSA formats, ABIF/SCF chromatograms, SnapGene DNA, annotations, variants, or regional read evidence.

Categories
Made by
OpenAI · Website
Sign-in
On Install
Capabilities
Interactive, Read, Write
Availability
Available
Version
0.1.53
Keywords
sequence, alignment, msa, fasta, fastq, genbank, embl, snapgene, sanger, abif, scf, a3m, stockholm, bioinformatics
Created
August 6, 2026
More info
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