Pathogen Variant Surveillance
Query live pathogen genomic surveillance data through the GenSpectrum LAPIS API to find which viral lineages are circulating now, how fast they are growing, and what mutations they carry. Use whenever a question depends on the current state of a pathogen population rather than on remembered facts - which SARS-CoV-2 variant is dominant, whether a Pango lineage is still designated or has been withdrawn, what clade or genotype of H5N1 is in a host or region, whether a PCR primer or assay target still matches circulating sequence, or how a lineage's prevalence has moved week to week. Triggers include "variant surveillance", "genomic surveillance", "what variant is circulating", "dominant variant", "Pango lineage", "lineage prevalence", "growth advantage", "SARS-CoV-2 variant", "XFG", "clade 2.3.4.4b", "H5N1 genotype", "influenza clade", "RSV/mpox/measles/dengue lineage", "CoV-Spectrum", "LAPIS", "Nextclade", "pango-designation", and any request to report what a pathogen population looks like today.
- Skill ID
- k-dense-ai/scientific-agent-skills/pathogen-variant-surveillance
- Publisher
- k-dense-ai
- Repository
- scientific-agent-skills
- Installs
- 0
- Files
- 9
- License
- MIT
- Requires
- Requires Python 3.11+. Scripts use only the standard library - no third-party packages. Needs network access to the public GenSpectrum LAPIS instances (lapis.cov-spectrum.org, lapis.genspectrum.org, lapis.pathoplexus.org) and to raw.githubusercontent.com for pango-designation. No API key.
- Synced
- Sep 23, 2026
Open any RiverX project, open the Skills panel in the chat, and search for this identifier. The files are fetched from the source repository at install time.
k-dense-ai/scientific-agent-skills/pathogen-variant-surveillanceInstalls these files- SKILL.md
- references/lapis-api.md
- references/lineage-nomenclature.md
- references/surveillance-caveats.md
- scripts/lapis_client.py
- scripts/lineage_prevalence.py
- scripts/mutation_profile.py
- scripts/reporting_lag.py
- scripts/resolve_lineage.py
What this skill tells the agent
Pathogen Variant Surveillance
When to use
Any time an answer depends on what a pathogen population looks like now: which lineages are circulating, whether one is growing, what a lineage name currently means, or whether an assay target still matches.
The rule
Never state what is circulating, and never write a lineage name, from memory.
Three things go wrong at once, and only the first is an ordinary knowledge-cutoff problem:
- Names post-date training. The Pango designation list carries over 6,200 names and grows continuously.
- The nomenclature is a live data structure, not a convention.
XFGis a recombinant that only resolves throughalias_key.json;PQ.17unaliases toXDV.1.5.1.1.8.1.17. Neither expansion is derivable by reasoning — the mapping is a file that changes. - Prior knowledge gets retracted, not just outdated. 294 names in the current
lineage_notes.txtare withdrawn or redesignated.PC.2is nowLF.7.9;XFG.20was withdrawn outright. A remembered lineage fact is not merely stale, it can be actively wrong.
Every number this skill reports is a count returned by a live instance, stamped with the data version it came from.
Scope
Surveillance data analysis for research. This skill describes sequences that were collected and submitted; it does not produce clinical interpretations, outbreak-response recommendations, or public-health guidance, and sequence counts are not case counts.
Instances
One API shape covers every pathogen. --instance names a verified deployment; --base-url reaches any other LAPIS instance.
| Instance | Host | Lineage column | Indexed |
|---|---|---|---|
sars-cov-2 | lapis.cov-spectrum.org (open GenBank data) | pangoLineage | yes |
h5n1, h3n2, h1n1pdm, influenza-a | lapis.genspectrum.org | clade | no |
rsv-a, rsv-b, mpox, measles, dengue, west-nile, hmpv, ebola-zaire, ebola-sudan, cchf | lapis.pathoplexus.org | varies | varies |
Field names differ per instance and are never assumed. Every script reads /sample/databaseConfig at run time and picks the collection-date, submission-date and lineage columns from what the instance actually declares. dateFrom= is correct on SARS-CoV-2 and a hard 400 on H5N1, whose collection date is sampleCollectionDateRangeLower.
Scripts
cd skills/pathogen-variant-surveillance/scripts| Script | Question answered |
|---|---|
resolve_lineage.py | Does this name still exist, what does it expand to, what is it descended from? |
lineage_prevalence.py | What share of sequences is this lineage, week by week, and is it growing? |
mutation_profile.py | What mutations does it carry, and how does it differ from another lineage? |
reporting_lag.py | How far back does the data have to go before it can be trusted? |
All four take --format table|tsv|json and print provenance (instance, data version, resolved field names, filters) to stderr, so > out.tsv keeps the data clean and the provenance visible.
Start from the data, not from a remembered list
# no names: discover what is actually circulating in the window
python3 lineage_prevalence.py --top 5 --where country=USA --weeks 12note: discovered the 5 most common pangoLineage values in the window: XFG.1.1, XFG.23.1.3, PY.1.1.1, XFJ.3.1.2, PQ.17
This is the right first command for "what is circulating". Naming lineages up front presumes you already know which ones matter, which is the assumption this skill exists to remove.
Check a name before using it
python3 resolve_lineage.py XFG.23.1.3 PQ.17 PC.2 NOTALINEAGEquery status unaliased parent recombinant_of descendants sequences detail
XFG.23.1.3 current XFG.23.1.3 XFG.23.1 LF.7+LP.8.1.2 6 317 S:A1174V, on C29137T branch
PQ.17 current XDV.1.5.1.1.8.1.17 NB.1.8.1 23 931 Alias of XDV.1.5.1.1.8.1.17
PC.2 withdrawn B.1.1.529.2.86.1.1.16.1.7.2.1.2 LF.7.2.1 4 25 now LF.7.9; Redesignated as LF.7.9
NOTALINEAGE unknown NOTALINEAGE 0 n/a no such name in the live nomenclature(detail abridged; each real row also cites the lineage proposal it came from.)
Exit code is 1 if any name is withdrawn or unknown, so it gates a manuscript's lineage list. Note PC.2: withdrawn upstream, yet 25 sequences still carry the label because the instance's assignments lag designation. Both facts are true and both matter.
Prevalence and growth
python3 lineage_prevalence.py "XFG.1.1*" "XFJ*" --where country=USA --weeks 16 --growthlineage week n total proportion ci_low ci_high coverage
XFG.1.1* 2026-05-04 42 80 0.5250 0.4170 0.6308 ok
XFG.1.1* 2026-06-15 3 49 0.0612 0.0210 0.1652 ok
XFG.1.1* 2026-06-29 1 30 0.0333 0.0059 0.1667 low
XFG.1.1* 2026-07-13 0 0 lowProportions carry Wilson intervals because surveillance weeks are small. Weeks whose denominator has not filled in yet are flagged low and excluded from the growth fit unless --include-incomplete.
The window is widened to whole ISO weeks, and says so when it does. A window starting mid-week would give a first row covering three days and a last row covering four, neither comparable to the full weeks between them.
--growth reports a weighted least-squares slope of log-odds against time. It is descriptive: it absorbs every change in who is sequencing, where, and how fast they report. It is not a fitness or transmissibility estimate. No slope is printed for a lineage with too few observations — see the trap table for why that guard exists.
Mutations, and whether an assay still matches
python3 mutation_profile.py "XFJ*" --versus "XFG*" --gene S --since 2026-01-01mutation gene position verdict prop_a prop_b n_a n_b
S:L441R S 441 gained 1.000 0.000 66 0
S:A475V S 475 gained 1.000 0.000 68 0
S:K444R S 444 lost 0.000 0.996 0 5031
S:Q493E S 493 lost 0.000 0.998 0 5359Works the same on a segmented genome — --instance h5n1 --gene HA or --gene seg4. Use --nucleotide for primer and probe questions, where the codon is not the unit that matters.
Decide how far back to trust
python3 reporting_lag.py --where country=USAlag_days mean_complete min_complete max_complete cohorts
14 0.456 0.332 0.557 6
30 0.677 0.580 0.822 6
60 0.868 0.802 0.949 6
90 0.939 0.916 1.000 690% of a cohort has arrived by 90 days. Trust collection dates up to 2026-04-28; treat anything later as provisional.
Run this before quoting any recent prevalence. The curve differs sharply by pathogen and country: on H5N1 the same measurement returns 0% complete at 14 days and 15% at 30 days, so a "current" H5N1 picture is effectively blind for two months.
Traps that produce silently wrong answers
All verified against the live API on 2026-07-27. These are why this skill ships scripts rather than a recipe; full detail in references/lapis-api.md.
| Trap | Consequence |
|---|---|
| A bare lineage name excludes its descendants | pangoLineage=XFG returns 4 sequences; XFG* returns 640 |
A trailing * needs a lineage index | On H5N1 clade=2.3.4.4b returns 62,413 and clade=2.3.4.4b* returns 0 — the same syntax, the opposite meaning |
| Field names are per-instance | dateFrom is a 400 on H5N1; the collection date is sampleCollectionDateRangeLower |
More from k-dense-ai
Use this skill in a project
Open any RiverX project, search the Skills panel for k-dense-ai/scientific-agent-skills/pathogen-variant-surveillance, and install it in one click.
