← Biological Sequence & Alignment ViewerCONTENT HISTORY

Update to Biological Sequence & Alignment Viewer

Snapshot Oct 27, 2026 · 00:20 UTC · version 0.1.53

WHAT CHANGED

Package or technical metadata updated

Package or technical metadata updated

Observed in package metadata. These changes alone do not establish a new customer-facing feature.

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Is v2 template

Before

Oct 24, 2026 · 13:04 UTC

Not present

After

Oct 27, 2026 · 00:20 UTC

false

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Full technical diff · 1 changed fields

added /is_v2_template

BEFORE
Field was absent
AFTER
false
Full snapshot data
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  "connector_id": null,
  "created_at": "2026-08-06T02:42:01.886962Z",
  "discoverability": "LISTED",
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  "is_template": false,
  "is_template_instance": false,
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  "name": "sequence-viewer",
  "release": {
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    "app_manifest": null,
    "app_templates": [],
    "description": "Inspect, analyze, safely edit, and compare biological sequences and alignments.",
    "display_name": "Biological Sequence & Alignment Viewer",
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    "interface": {
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      "capabilities": [
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      "category": "Scientific Research",
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      "composer_icon_url": "https://files.openai.com/content?id=file_00000000e21c81f795e54809feb9ec66",
      "default_prompt": "Fetch ENA DRR037765 first 500 reads to active workspace; open and report live length range, GC, Q30, and subset provenance",
      "default_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"
      ],
      "developer_name": "OpenAI",
      "logo_url": "https://files.openai.com/content?id=file_00000000aa28820c9928c8bfa150c88f",
      "logo_url_dark": null,
      "long_description": "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.",
      "plugin_category_id": "scientific research",
      "privacy_policy_url": "https://openai.com/policies/privacy-policy/",
      "screenshot_urls": [],
      "short_description": "Inspect, analyze, and compare biological sequences and alignments.",
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        "interface": {
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  "status": "ENABLED"
}

SHA-256 of public snapshot: 978c7b0dc671c2ce7fbf435362740d3de28f33b4d45e6701a16ba5c4f9232df9