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Get Started Free →Search the PRIDE Archive v3 REST API for proteomics datasets: discover projects by keyword + faceted filters (organism, instrument, disease, software), fetch project metadata, list and download RAW/PEAK/RESULT/FASTA files (with FTP/Aspera URLs), look up which projects mention a UniProt accession, and find similar projects. PRIDE v3 no longer exposes peptide/PSM-level identification endpoints — for spectrum-level data download the project's RESULT files. Use uniprot-protein-database for protein s
.claude/skills/jaechang-hits-pride-database/SKILL.md| Test case | Without → With | Effect | Δ tokens | Δ turns |
|---|---|---|---|---|
| case-15 | ✗→✓ | ▲ Improved | 223% | 0% |
| case-04 | ✗→✓ | ▲ Improved | 243% | 0% |
| case-05 | ✗→✓ | ▲ Improved | 258% | 0% |
| case-06 | ✗→✓ | ▲ Improved | 307% | 0% |
| case-07 | ✗→✓ | ▲ Improved | 441% | 0% |
The PRIDE Archive (ProteomicsIDEntifications database) at EMBL-EBI is the world's largest public mass-spectrometry proteomics repository — 39,000+ projects and 3.4M+ deposited files as of 2026. Programmatic access is via a JSON REST API at https://www.ebi.ac.uk/pride/ws/archive/v3/. No authentication is required. The OpenAPI/Swagger spec is at https://www.ebi.ac.uk/pride/ws/archive/v3/v3/api-docs. PRIDE v3 returns plain JSON arrays for list endpoints (no HAL+JSON _embedded envelope) and intentionally does not expose per-peptide or per-PSM identification endpoints — for spectrum-level identifications, download the project's RESULT files (mzIdentML, MaxQuant txt, etc.) and parse them locally.
uniprot-protein-databaseinterpro-database — PRIDE only reports project-level occurrence, not domain-level features/peptides, /psms, or /proteins?proteinAccession= endpoints — if you need peptide- or PSM-level data, download the RESULT files from /projects/{accession}/files and parse them with pyteomics or a search-engine-specific readerrequests, pandas, matplotlibPXD###### format) or a search keyword, optionally a UniProt accession for protein-occurrence lookuptime.sleep(0.3) in loopsbashpip install requests pandas matplotlib
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" # 1) Free-text search for cancer proteomics projects projects = requests.get(f"{PRIDE}/search/projects", params={"keyword": "prostate cancer", "pageSize": 5}, timeout=30).json() print(f"Top {len(projects)} projects:") for p in projects[:3]: instr = ", ".join(p.get("instruments", []))[:50] print(f" {p['accession']} {(p['title'] or '')[:70]} [{instr}]") # 2) Drill into one project acc = projects[0]["accession"] proj = requests.get(f"{PRIDE}/projects/{acc}", timeout=30).json() print(f"\n{proj['accession']}: {proj['title'][:70]}") print(f" Submitted: {proj.get('submissionDate')} DOI: {proj.get('doi')}") print(f" Organisms: {[o['name'] for o in proj.get('organisms', [])]}") print(f" Instruments: {[i['name'] for i in proj.get('instruments', [])]}") # 3) List files and total size files = requests.get(f"{PRIDE}/projects/{acc}/files/all", timeout=60).json() total_mb = sum(f.get("fileSizeBytes", 0) for f in files) / 1e6 print(f"\n {len(files)} files, {total_mb:.0f} MB total")
/search/projectsFree-text search with optional facet-based filtering, pagination, and sorting. Returns a plain JSON array of project records — there is no HAL+JSON _embedded/page wrapper.
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def search_projects(keyword=None, organism=None, instrument=None, disease=None, software=None, page_size=25, page=0, sort_field="submission_date", sort_direction="DESC"): """Search PRIDE v3 for projects. Filter syntax (for the `filter` arg) is `field==value, field==value` using `_facet` field names that are discoverable via /facet/projects.""" filters = [] if organism: filters.append(f"organisms_facet=={organism}") if instrument: filters.append(f"instruments_facet=={instrument}") if disease: filters.append(f"diseases_facet=={disease}") if software: filters.append(f"softwares_facet=={software}") params = {"pageSize": page_size, "page": page, "sortFields": sort_field, "sortDirection": sort_direction} if keyword: params["keyword"] = keyword if filters: params["filter"] = ",".join(filters) r = requests.get(f"{PRIDE}/search/projects", params=params, timeout=30) r.raise_for_status() return r.json() # plain list[dict] projects = search_projects(keyword="cancer", organism="Homo sapiens (human)", instrument="Q Exactive", page_size=5) df = pd.DataFrame([{ "accession": p["accession"], "title": (p.get("title") or "")[:70], "submission_date": p.get("submissionDate"), "diseases": ", ".join(p.get("diseases", []))[:60], "instruments": ", ".join(p.get("instruments", []))[:50], } for p in projects]) print(df.to_string(index=False))
python# Paginate through all matches for a keyword. The API doesn't return total counts inline; # walk pages until the next one is empty. def search_all_projects(keyword, page_size=100, max_pages=20): all_records, page = [], 0 while page < max_pages: batch = search_projects(keyword=keyword, page_size=page_size, page=page) if not batch: break all_records.extend(batch) if len(batch) < page_size: break # last page page += 1 return all_records results = search_all_projects("phosphoproteomics", page_size=100, max_pages=3) print(f"Phosphoproteomics projects collected (max 300): {len(results)}")
/facet/projectsBefore constructing a filtered search, query the facet endpoint to see which instrument / organism / disease / software values actually exist for a given keyword, along with their counts. The response is a dict of facet groups, each mapping {value: count}.
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def get_facets(keyword=None, facet_page_size=20): """Return facet counts for projects matching `keyword`. Keys are facet groups (instruments, organisms, diseases, softwares, experimentTypes, ...); values are dicts of {value: count}.""" params = {"facetPageSize": facet_page_size} if keyword: params["keyword"] = keyword r = requests.get(f"{PRIDE}/facet/projects", params=params, timeout=30) r.raise_for_status() return r.json() facets = get_facets(keyword="cancer", facet_page_size=10) print(f"Facet groups: {list(facets.keys())}") print(f"\nTop instruments for 'cancer':") for instr, n in sorted(facets.get("instruments", {}).items(), key=lambda kv: -kv[1])[:8]: print(f" {instr:<35} {n}") print(f"\nTop diseases:") for d, n in sorted(facets.get("diseases", {}).items(), key=lambda kv: -kv[1])[:6]: print(f" {d:<55} {n}")
/projects/{accession}Full metadata for a single project: submitters, labPIs, instruments, organisms (CV-coded), diseases, experiment types, references, DOI, submission/publication dates. Lists are CvParam-style objects with accession, cvLabel, name, optionally value.
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def get_project(accession): r = requests.get(f"{PRIDE}/projects/{accession}", timeout=30) r.raise_for_status() return r.json() p = get_project("PXD004131") print(f"Accession : {p['accession']}") print(f"Title : {p['title'][:80]}") print(f"Submission : {p.get('submissionDate')}") print(f"Publication : {p.get('publicationDate')}") print(f"DOI : {p.get('doi')}") print(f"License : {p.get('license')}") print(f"Type : {p.get('submissionType')}") print(f"Organisms : {[o['name'] for o in p.get('organisms', [])]}") print(f"Instruments : {[i['name'] for i in p.get('instruments', [])]}") print(f"Experiment : {[e['name'] for e in p.get('experimentTypes', [])]}") print(f"PIs : {[pi.get('name') for pi in p.get('labPIs', [])]}") print(f"References : {[r.get('doi') for r in p.get('references', [])[:3]]}")
/projects/{accession}/files + /files/allList the files associated with a project. Use the paginated endpoint for large projects; /files/all returns every file in one shot. Each file record carries fileCategory.value (one of RAW, PEAK, RESULT, FASTA, OTHER), fileSizeBytes (note the Bytes suffix — not fileSize), and a list of publicFileLocations each labeled FTP Protocol or Aspera Protocol.
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def get_project_files(accession, file_type=None, page_size=100): """Walk paginated /files for a project. Optionally filter by category code (RAW, PEAK, RESULT, FASTA, OTHER). Returns a DataFrame.""" rows, page = [], 0 while True: r = requests.get(f"{PRIDE}/projects/{accession}/files", params={"pageSize": page_size, "page": page}, timeout=30) r.raise_for_status() batch = r.json() if not batch: break for f in batch: cat = f.get("fileCategory") or {} ftp = next((loc["value"] for loc in f.get("publicFileLocations", []) if loc.get("name") == "FTP Protocol"), "") asp = next((loc["value"] for loc in f.get("publicFileLocations", []) if loc.get("name") == "Aspera Protocol"), "") rows.append({ "file_name": f.get("fileName"), "category": cat.get("value"), # RAW/PEAK/RESULT/FASTA/OTHER "size_mb": round((f.get("fileSizeBytes") or 0) / 1e6, 2), "ftp_url": ftp, "aspera_url": asp, "downloads": f.get("totalDownloads"), }) if len(batch) < page_size: break page += 1 df = pd.DataFrame(rows) if file_type: df = df[df["category"] == file_type] return df files_df = get_project_files("PXD004131") print(f"Total files: {len(files_df)}") print(files_df.groupby("category")["size_mb"].agg(["count", "sum"]).round(1).to_string()) raw_only = files_df[files_df["category"] == "RAW"] print(f"\nRAW files: {len(raw_only)}; combined {raw_only['size_mb'].sum():.0f} MB") print(raw_only[["file_name", "size_mb", "downloads"]].head(5).to_string(index=False))
python# /files/all returns every file in one response — convenient for small projects files = requests.get(f"{PRIDE}/projects/PXD000001/files/all", timeout=60).json() print(f"PXD000001 files (all): {len(files)}") for f in files[:4]: print(f" [{f.get('fileCategory',{}).get('value','?'):<6}] {f['fileName']} " f"{f.get('fileSizeBytes',0)/1e6:.2f} MB")
/files/sdrf/{projectAccession}PRIDE projects that follow the modern submission standard include an SDRF (Sample-Data Relationship Format) TSV that maps each MS run to its biological sample, treatment, label, fraction, etc. Pull it once, parse it as a TSV.
pythonimport requests, pandas as pd, io PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def get_sdrf(accession): """Fetch the SDRF sample-to-run mapping for a project (404 if not provided).""" r = requests.get(f"{PRIDE}/files/sdrf/{accession}", timeout=30) if r.status_code == 404: return None r.raise_for_status() return pd.read_csv(io.StringIO(r.text), sep="\t") # Many older projects have no SDRF — newer ones typically do sdrf = get_sdrf("PXD000001") if sdrf is None or sdrf.empty: print("No SDRF available for this project") else: print(f"SDRF rows: {len(sdrf)} cols: {len(sdrf.columns)}") print(f"First columns: {list(sdrf.columns)[:8]}")
/proteins/{accession}PRIDE v3's protein endpoint returns only the list of project accessions that contain identifications for the given UniProt accession. It does not return PSM counts, peptide counts, or sequence coverage — those are not exposed at the API surface in v3. For depth metrics you must download a project's RESULT files and parse them locally.
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def get_protein_projects(uniprot_acc): """Return the list of PRIDE project accessions that mention this UniProt accession. No PSM/peptide/coverage counts are available at this endpoint.""" r = requests.get(f"{PRIDE}/proteins/{uniprot_acc}", timeout=30) if r.status_code == 404: return None r.raise_for_status() data = r.json() return data.get("projects", []) tp53 = get_protein_projects("P04637") print(f"TP53 (P04637) is reported in {len(tp53)} PRIDE projects") print(f"First 8: {tp53[:8]}") unknown = get_protein_projects("Q99999") print(f"\nQ99999 (no real protein): " f"{'no PRIDE evidence' if not unknown else f'{len(unknown)} projects'}")
/projects/{accession}/similarProjects returns projects with related metadata signatures (organism, instrument, experiment type, tags). /search/autocomplete?keyword=... returns project titles starting with the prefix — useful to suggest searches.
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" # Find similar projects to one of interest similar = requests.get(f"{PRIDE}/projects/PXD004131/similarProjects", params={"pageSize": 5}, timeout=30).json() print(f"Similar to PXD004131: {len(similar)} projects") for p in similar[:5]: print(f" {p['accession']} {(p.get('title') or '')[:70]}") # Autocomplete suggestions for a project-title prefix suggestions = requests.get(f"{PRIDE}/search/autocomplete", params={"keyword": "tp53"}, timeout=30).json() print(f"\nAutocomplete for 'tp53': {len(suggestions)} suggestions") for s in suggestions[:5]: print(f" {s}")
/projects/count, /files/countGet total counts across the repository — useful for status displays and sanity checks. Both endpoints return a plain integer body (no JSON object wrapper).
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" n_projects = int(requests.get(f"{PRIDE}/projects/count", timeout=30).text) n_files = int(requests.get(f"{PRIDE}/files/count", timeout=30).text) print(f"PRIDE Archive current scale:") print(f" Projects: {n_projects:,}") print(f" Files: {n_files:,}")
PRIDE v3 list endpoints return plain JSON arrays — for example /search/projects returns [{...}, {...}, ...] directly. There is no _embedded.compactprojects, no page.totalElements/totalPages, no _links.next.href. Older PRIDE v2 clients that parsed data["_embedded"]["compactprojects"] will silently return empty against the current API. To paginate, walk page=0, 1, 2, ... until you get an empty array (or a partial page shorter than pageSize).
The endpoint families below no longer exist in v3 (and v2 is now an alias for v3 internally — error messages from /v2/peptides literally report path: "/pride/ws/archive/v3/peptides"):
| Removed endpoint | Status in v3 | Replacement | |---|---|---| | GET /peptides?projectAccessions=X | 404 | None — download project's RESULT files and parse | | GET /psms?projectAccessions=X | 404 | None — download RESULT files | | GET /proteins?proteinAccession=X (query-param style) | 404 | GET /proteins/{accession} (path-param) | | HAL+JSON _embedded/page wrapper | Gone | Plain JSON array | | /projects?keyword=...&organisms=...&tissues=... filters | Silently ignored | /search/projects?keyword=...&filter=field==value |
/search/projectsThe filter query parameter takes a comma-separated list of field==value constraints. Field names use the _facet suffix (the underlying Solr-style field). Discover valid field names and values via /facet/projects before constructing the filter:
python# Valid filter forms "organisms_facet==Homo sapiens (human)" "instruments_facet==Q Exactive" "diseases_facet==Prostate adenocarcinoma" "softwares_facet==MaxQuant" # Combine with commas filter="organisms_facet==Homo sapiens (human),instruments_facet==Orbitrap Fusion Lumos"
Each file in a project carries a fileCategory CV-param. The .value is a category code; the .name is the human-readable label:
| value code | Description | Common formats | |---|---|---| | RAW | Unprocessed instrument output | .raw (Thermo), .d (Bruker/Agilent), .wiff (Sciex) | | PEAK | Centroided / deconvoluted spectra | .mzML, .mzXML, .mgf | | RESULT | Identification results | .mzid, .mzTab, MaxQuant txt, PRIDE XML | | FASTA | Protein sequence database used in search | .fasta | | OTHER | Supplementary / scripts / tables | .txt, .xlsx, .csv |
For reanalysis pipelines, RESULT is the cheapest entry point — pre-identified peptides without re-searching spectra. PEAK lets you re-search with a different engine. RAW is only needed for full vendor-format reprocessing.
PRIDE project accessions follow ProteomeXchange format PXD######. These are stable across PRIDE, MassIVE, jPOST, and iProX. File accessions inside PRIDE are SHA-256-style hashes (e.g., 5bda360133398f66021c8889e01dce921cb51300c7269e1f2b0f20368ab20af6) — opaque identifiers; use fileName for human-readable filenames.
Goal: Start from a disease keyword, see which instruments and softwares are common in matching datasets via facet counts, then pull a filtered project list using one of the top values.
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" disease_kw = "colorectal cancer" # 1) Inspect facet counts to learn which filter values dominate facets = requests.get(f"{PRIDE}/facet/projects", params={"keyword": disease_kw, "facetPageSize": 10}, timeout=30).json() top_instr = sorted(facets.get("instruments", {}).items(), key=lambda kv: -kv[1])[:5] top_org = sorted(facets.get("organisms", {}).items(), key=lambda kv: -kv[1])[:3] print(f"Top instruments for '{disease_kw}':") for k, v in top_instr: print(f" {k:<35} {v}") print(f"Top organisms:") for k, v in top_org: print(f" {k:<35} {v}") # 2) Build a filtered search using one top instrument target_instr = top_instr[0][0] projects = requests.get(f"{PRIDE}/search/projects", params={"keyword": disease_kw, "filter": f"organisms_facet==Homo sapiens (human),instruments_facet=={target_instr}", "pageSize": 50, "sortFields": "submission_date", "sortDirection": "DESC"}, timeout=30).json() df = pd.DataFrame([{ "accession": p["accession"], "title": (p.get("title") or "")[:70], "submission_date": p.get("submissionDate"), "tissues": ", ".join(p.get("organismsPart", []))[:40], "submitter": (p.get("submitters") or [""])[0] if p.get("submitters") else "", } for p in projects]) print(f"\nFiltered projects: {len(df)} (target instrument: {target_instr})") print(df.head(10).to_string(index=False)) df.to_csv(f"{disease_kw.replace(' ', '_')}_{target_instr.replace(' ', '_')}_projects.csv", index=False)
Goal: Pull the file list for a project, filter to the categories you actually want (RAW + RESULT), and emit an aria2c-ready URL list for parallel FTP download.
pythonimport requests, pandas as pd from pathlib import Path PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" accession = "PXD004131" keep_categories = {"RAW", "RESULT"} output_dir = Path(f"/data/pride/{accession}") files = requests.get(f"{PRIDE}/projects/{accession}/files/all", timeout=120).json() manifest = [] for f in files: cat = (f.get("fileCategory") or {}).get("value") if cat not in keep_categories: continue ftp = next((loc["value"] for loc in f.get("publicFileLocations", []) if loc.get("name") == "FTP Protocol"), None) if not ftp: continue manifest.append({ "file_name": f["fileName"], "category": cat, "size_mb": round((f.get("fileSizeBytes") or 0) / 1e6, 2), "ftp": ftp, }) mdf = pd.DataFrame(manifest).sort_values(["category", "file_name"]) print(f"{accession}: keeping {len(mdf)}/{len(files)} files " f"({mdf['size_mb'].sum():.0f} MB total)") print(mdf.groupby("category")[["size_mb"]].sum().round(0)) # aria2c -i pride_dl.list -d /data/pride/PXD004131 -x 8 -j 4 with open("pride_dl.list", "w") as fh: fh.write("\n".join(mdf["ftp"])) print(f"\nWrote pride_dl.list with {len(mdf)} URLs (use aria2c -i)")
Goal: For a candidate protein panel (e.g., from a differential-expression analysis), look up how many PRIDE projects mention each one and shortlist the most-evidenced proteins. Note: this is a project-count signal only — there are no PSM/peptide counts at the API surface in v3, so a high project count is breadth, not depth.
pythonimport requests, time, pandas as pd, matplotlib.pyplot as plt PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" candidates = { "P04637": "TP53", "P38398": "BRCA1", "P31749": "AKT1", "P40763": "STAT3", "O15530": "PDPK1", "P10275": "AR", } rows = [] for acc, sym in candidates.items(): r = requests.get(f"{PRIDE}/proteins/{acc}", timeout=30) projs = r.json().get("projects", []) if r.status_code == 200 else [] rows.append({"uniprot": acc, "symbol": sym, "n_projects": len(projs)}) time.sleep(0.3) df = pd.DataFrame(rows).sort_values("n_projects", ascending=False) print(df.to_string(index=False)) fig, ax = plt.subplots(figsize=(8, 3.5)) bars = ax.bar(df["symbol"], df["n_projects"], color="#3182BD") ax.bar_label(bars, fmt="%d", fontsize=9, padding=2) ax.set_ylabel("# PRIDE projects mentioning the protein") ax.set_title("PRIDE project-level occurrence — candidate panel") plt.tight_layout() plt.savefig("pride_protein_occurrence.png", dpi=150, bbox_inches="tight") print("Saved pride_protein_occurrence.png")
| Parameter | Endpoint | Default | Range / Options | Effect | |---|---|---|---|---| | keyword | /search/projects, /facet/projects, /search/autocomplete | — | free-text string | Full-text search across title, description, tags | | filter | /search/projects | — | field_facet==value, field_facet==value | Server-side filter using facet field names | | pageSize | /search/projects, /projects, /projects/{acc}/files, /projects/{acc}/similarProjects | 100 | positive integer | Results per page | | page | same as above | 0 | 0-indexed integer | Page number (no metadata returned — walk pages until empty) | | sortFields | /search/projects | submission_date | comma-separated field names | Sort key(s) | | sortDirection | /search/projects | DESC | ASC or DESC | Sort order | | facetPageSize | /facet/projects | 20 | positive integer | Values returned per facet group | | dateGap | /search/projects, /facet/projects | — | e.g. +1MONTH, +1YEAR | Date-range aggregation granularity | | (path) accession | /projects/{acc}, /projects/{acc}/files, /projects/{acc}/similarProjects, /proteins/{acc} | required | PXD###### or UniProt acc | Identifies the resource |
/search/projects for searching, not /projects. Plain /projects is a paginated listing endpoint and silently ignores keyword / organism / disease filters. Filtering only works through /search/projects with the filter=field_facet==value syntax./facet/projects before filtering. Facet field values must match exactly (e.g., organisms_facet==Homo sapiens (human), parentheses and all). The facet endpoint tells you which values exist and how many projects each has — saves a lot of trial-and-error.pyteomics, pyOpenMS, or a search-engine reader (MaxQuant, ProteomeDiscoverer, etc.).FTP Protocol and Aspera Protocol URLs. FTP is more universally supported; pair it with aria2c -x 8 -j 4 for parallel chunks. Use Aspera only if you have an Aspera client and need >100 Mbit transfer speeds.fileSizeBytes. The current v3 field is fileSizeBytes, not fileSize (old v2 docs may say fileSize). Sizes are in bytes — divide by 1e6 for MB, 1e9 for GB.fileCategory.value. A project can have hundreds of files spanning RAW (GB-scale) and OTHER (KB-scale). Always filter to the categories you actually need before queueing downloads — otherwise you'll easily download tens of gigabytes of vendor RAW files when you only wanted the identification tables.totalElements/totalPages. Iterate page=0, 1, 2, ... and stop when a page returns an empty array, or when its length is less than pageSize.pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def project_file_summary(accession): files = requests.get(f"{PRIDE}/projects/{accession}/files/all", timeout=60).json() by_cat = {} for f in files: cat = (f.get("fileCategory") or {}).get("value", "OTHER") by_cat.setdefault(cat, [0, 0]) by_cat[cat][0] += 1 by_cat[cat][1] += (f.get("fileSizeBytes") or 0) / 1e6 print(f"\n{accession} file summary:") for cat, (n, mb) in sorted(by_cat.items()): print(f" {cat:<8} {n:>4} file(s) {mb:>10.1f} MB") total_mb = sum(mb for _, mb in by_cat.values()) total_n = sum(n for n, _ in by_cat.values()) print(f" {'TOTAL':<8} {total_n:>4} file(s) {total_mb:>10.1f} MB") project_file_summary("PXD000001")
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" def pride_evidence(uniprot_acc): """Return (has_evidence, n_projects). PRIDE v3 only exposes project list, no PSM counts.""" r = requests.get(f"{PRIDE}/proteins/{uniprot_acc}", timeout=30) if r.status_code != 200: return False, 0 projs = r.json().get("projects", []) return bool(projs), len(projs) for acc in ["P04637", "Q99999"]: has, n = pride_evidence(acc) print(f"{acc}: evidence={has} projects={n}")
pythonimport requests, pandas as pd PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" r = requests.get(f"{PRIDE}/search/projects", params={"keyword": "single-cell proteomics", "sortFields": "submission_date", "sortDirection": "DESC", "pageSize": 15}, timeout=30) recent = r.json() df = pd.DataFrame([{ "submission_date": p.get("submissionDate"), "accession": p["accession"], "title": (p.get("title") or "")[:80], } for p in recent]).sort_values("submission_date", ascending=False) print(df.to_string(index=False))
pythonimport requests PRIDE = "https://www.ebi.ac.uk/pride/ws/archive/v3" for prefix in ["alzheimer", "single cell", "brca"]: s = requests.get(f"{PRIDE}/search/autocomplete", params={"keyword": prefix}, timeout=30).json() print(f"\n'{prefix}' → {len(s)} suggestions:") for sug in s[:3]: print(f" · {sug[:80]}")
| Problem | Cause | Solution | |---|---|---| | Parsing returns empty list even when r.json() has data | Code is doing data["_embedded"]["compactprojects"] — old HAL+JSON wrapper that v3 no longer returns | Parse the response directly as a list: projects = r.json() | | HTTP 404 on /peptides, /psms, or /proteins?proteinAccession=X | These endpoints were removed in v3 | For peptide/PSM data, download the project's RESULT files and parse locally. For protein lookup, use /proteins/{accession} (path param) | | /projects?keyword=cancer returns the same 100 results as /projects with no keyword | The /projects endpoint only accepts pageSize / page — keyword and other filters are silently ignored | Use /search/projects?keyword=...&filter=... instead | | /projects/{acc}/files shows file size 0 | Reading fileSize instead of fileSizeBytes | The v3 field is fileSizeBytes (bytes); compute MB via fileSizeBytes / 1e6 | | Filter has no effect | Facet value doesn't exactly match a real value | Call /facet/projects?keyword=... first to enumerate valid values (Homo sapiens (human), not Homo sapiens) | | pageSize beyond the actual result set returns an empty array | Normal pagination behavior | Stop iterating when the returned array length is < pageSize, or when it is empty | | findAllOrganismsCount returns HTTP 406 Not Acceptable | The endpoint requires a non-JSON Accept header | Skip this endpoint — facet counts via /facet/projects cover the same need | | HTTP 429 or ConnectionError on bursts | Shared EBI infrastructure | Add time.sleep(0.3) in loops; retry on 5xx with exponential backoff |
uniprot-protein-database — UniProt sequences, Swiss-Prot annotations, ID mapping; pair with PRIDE protein lookups to enrich each UniProt accession with sequence and functional informationinterpro-database — Protein domain architecture (Pfam, SMART, PANTHER) for proteins reported in PRIDEpdb-database — Resolved 3D structures for proteins with PRIDE evidencepyteomics (off-skill Python library) — Parse mzIdentML / mzML / mzTab files downloaded from /projects/{accession}/files; the path for spectrum- and PSM-level analysis now that the REST API no longer exposes those/files/sdrf/{projectAccession}| Case | Status | Duration (ms) | Turns | Tokens | Tool calls | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Without | With | Δ | Without | With | Δ | Without | With | Δ | Without | With | Δ | ||
case-15 | fail→pass | 15,852 | 5,208 | -67% | 1 | 1 | 0% | 3,292 | 10,643 | +223% | 0 | 0 | — |
case-01 | pass→pass | 10,907 | 12,021 | +10% | 1 | 1 | 0% | 2,292 | 11,328 | +394% | 0 | 0 | — |
case-02 | pass→pass | 13,766 | 14,664 | +7% | 1 | 1 | 0% | 2,645 | 12,200 | +361% | 0 | 0 | — |
case-03 | pass→pass | 17,550 | 10,323 | -41% | 1 | 1 | 0% | 3,831 | 11,844 | +209% | 0 | 0 | — |
case-04 | fail→pass | 18,217 | 11,915 | -35% | 1 | 1 | 0% | 3,524 | 12,095 | +243% | 0 | 0 | — |
case-05 | fail→pass | 14,314 | 7,184 | -50% | 1 | 1 | 0% | 3,109 | 11,137 | +258% | 0 | 0 | — |
case-06 | fail→pass | 15,010 | 10,546 | -30% | 1 | 1 | 0% | 2,899 | 11,801 | +307% | 0 | 0 | — |
case-07 | fail→pass | 10,669 | 4,433 | -58% | 1 | 1 | 0% | 1,922 | 10,393 | +441% | 0 | 0 | — |
case-08 | pass→pass | 13,338 | 31,331 | +135% | 1 | 1 | 0% | 2,766 | 11,550 | +318% | 0 | 0 | — |
case-09 | fail→pass | 16,626 | 7,284 | -56% | 1 | 1 | 0% | 2,932 | 10,953 | +274% | 0 | 0 | — |
case-10 | fail→pass | 12,081 | 8,915 | -26% | 1 | 1 | 0% | 2,348 | 11,336 | +383% | 0 | 0 | — |
case-11 | fail→pass | 12,814 | 7,146 | -44% | 1 | 1 | 0% | 2,371 | 10,876 | +359% | 0 | 0 | — |
case-12 | fail→pass | 16,732 | 12,350 | -26% | 1 | 1 | 0% | 3,601 | 12,037 | +234% | 0 | 0 | — |
case-13 | fail→pass | 11,799 | 8,159 | -31% | 1 | 1 | 0% | 2,418 | 11,138 | +361% | 0 | 0 | — |
case-14 | fail→pass | 16,801 | 16,955 | +1% | 1 | 1 | 0% | 3,509 | 10,916 | +211% | 0 | 0 | — |
case-16 | fail→pass | 17,203 | 7,344 | -57% | 1 | 1 | 0% | 3,564 | 11,077 | +211% | 0 | 0 | — |
case-17 | fail→pass | 17,163 | 5,955 | -65% | 1 | 1 | 0% | 3,378 | 10,607 | +214% | 0 | 0 | — |
case-18 | pass→pass | 10,755 | 7,773 | -28% | 1 | 1 | 0% | 2,254 | 11,191 | +396% | 0 | 0 | — |
case-19 | fail→pass | 12,609 | 3,102 | -75% | 1 | 1 | 0% | 2,423 | 10,236 | +322% | 0 | 0 | — |
case-20 | fail→pass | 14,406 | 9,935 | -31% | 1 | 1 | 0% | 2,789 | 11,691 | +319% | 0 | 0 | — |
case-21 | fail→pass | 8,326 | 3,501 | -58% | 1 | 1 | 0% | 1,724 | 10,316 | +498% | 0 | 0 | — |
case-22 | pass→pass | 10,432 | 16,891 | +62% | 1 | 1 | 0% | 2,055 | 10,762 | +424% | 0 | 0 | — |
DecimalAI ran this skill against gemini-3.6-flash twice over the same eval suite — once with the skill loaded and once without — and compared the two runs case by case. 22 cases were attempted. The headline lift of +73 percentage points is the difference between those two pass rates over the 22 comparable cases.
Without the skill loaded, the model failed this case. With it loaded, the same prompt on the same model passed. This is one improved case from the latest verified run; every case, including any that regressed, is in the table above.
Other measured skills in the registry, with their headline benchmark lift.