Skip to content
cccskills
FreePublished on GitHub

metabolomics-workbench-database

Query Metabolomics Workbench REST API (4,200+ NIH studies) for metabolite ID, study discovery, RefMet standardization, m/z precursor searches, and gene/protein annotations. Quirks: compound input_item rejects `name` (use pubchem_cid/kegg_id/inchi_key/etc.); free-text → compound is a two-step refmet/match→refmet/name flow; moverz endpoint returns TSV text, not JSON. Use hmdb-database for local XML; pubchem-compound-search for general compound lookup.

The English summary is being prepared. Showing the original description.

See how to install

Files included (1)

  • SKILL.md20.8 KB

SKILL.md (original)

Review the instructions the agent will receive before you install.

Metabolomics Workbench Database — REST API Access

Overview

The Metabolomics Workbench (MW) REST API at https://www.metabolomicsworkbench.org/rest/ exposes 4,200+ metabolomics studies hosted at UCSD under NIH Common Fund sponsorship. URL pattern is /{context}/{input_item}/{input_value}/{output_item}/{format}. Contexts include compound, refmet, moverz, study, analysis, metabolite, gene, protein. Notable quirks discovered live:

  • compound/name/{x} is rejected — name is not an allowed input_item. Use pubchem_cid, kegg_id, inchi_key, hmdb_id, regno, lm_id, formula, smiles, or abbrev. For free-text input, go through refmet/match/{x} first.
  • refmet/name/{x}/all requires the exact RefMet name (e.g. Glucose, not D-glucose); use refmet/match/{x} for fuzzy normalisation first.
  • moverz/{REFMET|LIPIDS|MB}/{mz}/{ion}/{tol}/txt returns TSV text (no JSON variant).
  • The metstat/filter/... endpoint shown in older examples returns [] — replace with study/{context}/{value}/summary (or /metabolites) + client-side filtering.

No authentication required.

When to Use

  • Searching metabolite records by PubChem CID, KEGG ID, InChIKey, HMDB ID, formula, or SMILES
  • Discovering studies by species, disease, last_name, institute, analysis_type, or polarity
  • Standardising metabolite names to RefMet nomenclature for cross-study integration
  • Identifying unknown compounds from MS m/z values with adduct-aware matching (moverz)
  • Retrieving experimental metabolite tables (analyses, abundances) from published studies
  • Querying gene/protein annotations linked to metabolomics pathways
  • Downloading raw mwTab files for local analysis
  • For local 220K-metabolite XML parsing with NMR/MS spectra use hmdb-database instead
  • For live 110M-compound property lookups use pubchem-compound-search instead

Prerequisites

  • Python packages: requests, pandas
  • No API key required: publicly accessible
  • Rate limits: MW does not enforce strict limits; add time.sleep(0.3) between bulk requests
  • Base URL: https://www.metabolomicsworkbench.org/rest
pip install requests pandas

Quick Start

import requests

BASE = "https://www.metabolomicsworkbench.org/rest"

# Two-step free-text → compound (the API rejects compound/name/...)
def lookup_by_name(name):
    # 1) Normalise to RefMet name
    r = requests.get(f"{BASE}/refmet/match/{name}", timeout=30)
    r.raise_for_status()
    refmet = r.json()
    if not refmet.get("refmet_name"):
        return None
    # 2) Pull full compound record by RefMet name (or by pubchem_cid)
    r2 = requests.get(f"{BASE}/refmet/name/{refmet['refmet_name']}/all", timeout=30)
    rec = r2.json() if r2.json() else {}
    return rec if isinstance(rec, dict) else None

c = lookup_by_name("glucose")
print(f"{c['name']}: formula={c['formula']}, PubChem CID={c['pubchem_cid']}, "
      f"InChIKey={c['inchi_key']}")
# Glucose: formula=C6H12O6, PubChem CID=5793, InChIKey=WQZGKKKJIJFFOK-GASJEMHNSA-N

Core API

Module 1: Compound Queries

compound/{input_item}/{input_value}/all/json — input_item must be one of regno, formula, inchi_key, lm_id, pubchem_cid, hmdb_id, kegg_id, smiles, abbrev. The legacy name input is rejected by the server.

import requests

BASE = "https://www.metabolomicsworkbench.org/rest"

# By PubChem CID
r = requests.get(f"{BASE}/compound/pubchem_cid/5793/all/json", timeout=30)
glucose = r.json()
print(f"PubChem 5793 -> {glucose['name']}, formula={glucose['formula']}, "
      f"HMDB={glucose.get('hmdb_id')}, KEGG={glucose.get('kegg_id')}")

# By KEGG ID
r = requests.get(f"{BASE}/compound/kegg_id/C00031/all/json", timeout=30)
print("KEGG C00031 ->", r.json()["name"])

# By InChIKey
r = requests.get(f"{BASE}/compound/inchi_key/WQZGKKKJIJFFOK-GASJEMHNSA-N/all/json", timeout=30)
print("InChIKey -> regno:", r.json()["regno"])
# Compound by formula returns a paged dict (multiple matches)
import requests
BASE = "https://www.metabolomicsworkbench.org/rest"
r = requests.get(f"{BASE}/compound/formula/C6H12O6/all/json", timeout=30)
matches = r.json()
print(f"Compounds with formula C6H12O6: {len(matches)}")
for k in list(matches)[:3]:
    print(f"  regno={matches[k]['regno']}  name={matches[k]['name']}")

Module 2: Study Discovery

study/{input_item}/{input_value}/{output} — input_item includes study_id, study_title, last_name, institute, analysis_id, metabolite_id, kegg_id, refmet_name. output includes summary, metabolites, factors, data, available_studies, species, disease. summary for study_id returns a dict (keyed by accession when multiple); for last_name/institute it returns a list.

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

# Single-study summary — `study/study_id/{id}/summary` returns a flat dict
# (keys: study_id, study_title, species, institute, analysis_type, ...)
r = requests.get(f"{BASE}/study/study_id/ST000001/summary", timeout=30)
s = r.json()
print(f"{s['study_id']}: {s['study_title'][:60]}")
print(f"  Species : {s.get('species')}  Institute: {s.get('institute')}")
print(f"  Submit  : {s.get('submission_date')}")
# Studies that detected a metabolite — `study/refmet_name/{x}/summary` returns
# a thin index of (refmet_name, kegg_id, study_id) rows. Chain study_id → full summary
# to get title and species.
import requests, pandas as pd
BASE = "https://www.metabolomicsworkbench.org/rest"
r = requests.get(f"{BASE}/study/refmet_name/Glucose/summary", timeout=60)
d = r.json()
rows = list(d.values()) if isinstance(d, dict) else d
print(f"Studies referencing 'Glucose': {len(rows)}")
print(pd.DataFrame(rows).head(5).to_string(index=False))
# refmet_name kegg_id  study_id
#     Glucose  C00031  ST000001
#     Glucose  C00031  ST000002
#     ...

Module 3: RefMet Standardisation

refmet/match/{user_text} is a fuzzy normaliser — returns the standard RefMet record (no pubchem_cid/kegg_id though). refmet/name/{exact_refmet_name}/all returns the full record including IDs. Use them as a two-step pipeline.

import requests

BASE = "https://www.metabolomicsworkbench.org/rest"

def normalise_to_refmet(user_text):
    r = requests.get(f"{BASE}/refmet/match/{user_text}", timeout=30)
    r.raise_for_status()
    m = r.json()
    if not m or not m.get("refmet_name"):
        return None
    return m["refmet_name"]

def refmet_full(refmet_name):
    r = requests.get(f"{BASE}/refmet/name/{refmet_name}/all", timeout=30)
    r.raise_for_status()
    rec = r.json()
    return rec if isinstance(rec, dict) and rec else None

name = normalise_to_refmet("alpha-D-glucose")  # -> 'Glucose'
print(f"Normalised: {name}")
rec = refmet_full(name)
print(f"  PubChem CID : {rec['pubchem_cid']}")
print(f"  InChIKey    : {rec['inchi_key']}")
print(f"  Super class : {rec['super_class']} / {rec['main_class']} / {rec['sub_class']}")

Module 4: Study Filtering (replaces broken metstat)

The older metstat/filter/... endpoint returns []. Use the study context endpoints with client-side filtering instead.

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

def study_ids_for_metabolite(refmet_name):
    """Return the study_id list that report a given RefMet name."""
    r = requests.get(f"{BASE}/study/refmet_name/{refmet_name}/summary", timeout=60)
    r.raise_for_status()
    d = r.json()
    rows = list(d.values()) if isinstance(d, dict) else d
    return sorted({row["study_id"] for row in rows if row.get("study_id")})

def study_summary(study_id):
    """Pull full summary (title, species, institute, dates) for one study_id.
    Response is a flat dict with keys study_id/study_title/species/institute/..."""
    return requests.get(f"{BASE}/study/study_id/{study_id}/summary", timeout=30).json()

# Find glucose studies, then enrich the first few
ids = study_ids_for_metabolite("Glucose")
print(f"Studies referencing 'Glucose': {len(ids)}")
rows = [study_summary(sid) for sid in ids[:5]]
df = pd.DataFrame(rows)
print(df[["study_id", "study_title", "species"]].head().to_string(index=False))

Module 5: m/z Precursor Search (moverz)

moverz/{REFMET|LIPIDS|MB}/{mz}/{ion}/{tolerance}/txt returns tab-separated text (not JSON). The first DB selector (REFMET, LIPIDS, or MB) is required — mz as the first segment is rejected.

import requests, io, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

def moverz_search(db, mz, ion, tolerance=0.005):
    """Search precursor m/z in REFMET / LIPIDS / MB and return a DataFrame.
    Response is TSV text — no JSON variant."""
    assert db in {"REFMET", "LIPIDS", "MB"}
    r = requests.get(f"{BASE}/moverz/{db}/{mz}/{ion}/{tolerance}/txt", timeout=30)
    r.raise_for_status()
    return pd.read_csv(io.StringIO(r.text), sep="\t")

df = moverz_search("REFMET", 180.063, "M+H", 0.005)
print(f"Candidates at m/z 180.063 [M+H]+ (REFMET): {len(df)}")
print(df.head(5).to_string(index=False))
# Same query against the LIPIDS database
import requests, io, pandas as pd
BASE = "https://www.metabolomicsworkbench.org/rest"
r = requests.get(f"{BASE}/moverz/LIPIDS/760.585/M+H/0.01/txt", timeout=30)
df_lipids = pd.read_csv(io.StringIO(r.text), sep="\t")
print(f"Lipid candidates at m/z 760.585: {len(df_lipids)}")
print(df_lipids.head(3).to_string(index=False))

Module 6: Genes and Proteins

import requests

BASE = "https://www.metabolomicsworkbench.org/rest"

r = requests.get(f"{BASE}/gene/gene_symbol/HMGCR/all", timeout=30)
g = r.json()
print(f"{g['gene_symbol']} -> MGP: {g.get('mgp_id')}  ({g.get('gene_name', '')[:60]})")

# Protein by UniProt accession
r2 = requests.get(f"{BASE}/protein/uniprot_id/P04035/all", timeout=30)
p = r2.json()
print(f"UniProt P04035: {p.get('protein_name', '')[:60]}  organism={p.get('organism')}")

Key Concepts

Allowed input_item Values per Context

ContextValid input_itemNotes
compoundregno, formula, inchi_key, lm_id, pubchem_cid, hmdb_id, kegg_id, smiles, abbrevname is rejected — go via refmet/match first
refmetmatch, name, formula, exactmass, inchi_key, pubchem_cid, regnomatch is fuzzy; name requires the canonical RefMet name
studystudy_id, study_title, last_name, institute, analysis_id, metabolite_id, kegg_id, refmet_namesummary for study_id is a dict keyed by accession; for last_name/institute it's a list
moverz(path) REFMET / LIPIDS / MBFirst segment is the DB, not mz
genegene_id, gene_symbol, gene_name, mgp_idReturns a dict
proteinmgp_id, gene_id, uniprot_id, gene_symbolReturns a dict

Output Type Conventions

  • output=summary returns a dict when the input identifier is unique (e.g. study_id), a list when it isn't (e.g. last_name).
  • Appending /json to study/.../summary flips the response to TSV. Omit the format suffix — JSON is the default.
  • moverz only emits /txt (TSV); there is no JSON variant.

refmet/match vs refmet/name

  • refmet/match/{user_text} — fuzzy. Always returns a single dict with refmet_name, formula, exactmass, classification. Does not include pubchem_cid/inchi_key.
  • refmet/name/{exact_refmet_name}/all — requires the canonical RefMet name. Returns the full record including IDs. Returns an empty list if the name isn't canonical.

Common Workflows

Workflow 1: Free-Text → Full Compound Record

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

def resolve_to_compound(user_text):
    # 1) Normalise via refmet/match
    rm = requests.get(f"{BASE}/refmet/match/{user_text}", timeout=30).json()
    if not rm.get("refmet_name"):
        return None
    name = rm["refmet_name"]
    # 2) Fetch full RefMet record (includes pubchem_cid / inchi_key)
    full = requests.get(f"{BASE}/refmet/name/{name}/all", timeout=30).json()
    if not isinstance(full, dict) or not full:
        return None
    # 3) Optionally pull the matching compound record via PubChem CID
    cid = full.get("pubchem_cid")
    compound = None
    if cid:
        compound = requests.get(f"{BASE}/compound/pubchem_cid/{cid}/all/json",
                                timeout=30).json()
    return {
        "input": user_text,
        "refmet_name": name,
        "formula": full.get("formula"),
        "pubchem_cid": cid,
        "hmdb_id": compound.get("hmdb_id") if compound else None,
        "kegg_id": compound.get("kegg_id") if compound else None,
        "inchi_key": full.get("inchi_key"),
    }

queries = ["glucose", "alpha-D-glucose", "L-tyrosine", "cholesterol"]
df = pd.DataFrame([resolve_to_compound(q) for q in queries])
print(df.to_string(index=False))
df.to_csv("name_resolution.csv", index=False)

Workflow 2: Annotate MS Hit List

Goal: Take a list of measured m/z values and assign RefMet candidate compounds.

import requests, io, pandas as pd, time

BASE = "https://www.metabolomicsworkbench.org/rest"

def annotate_peaks(mz_values, ion="M+H", tolerance=0.005):
    out = []
    for mz in mz_values:
        r = requests.get(f"{BASE}/moverz/REFMET/{mz}/{ion}/{tolerance}/txt", timeout=30)
        if r.status_code != 200 or not r.text.strip():
            time.sleep(0.3); continue
        df = pd.read_csv(io.StringIO(r.text), sep="\t")
        for _, row in df.iterrows():
            out.append({
                "query_mz": mz,
                "matched_mz": row["Matched m/z"],
                "delta": row["Delta"],
                "name": row["Name"],
                "formula": row["Formula"],
                "ion": row["Ion"],
                "main_class": row.get("Main class"),
            })
        time.sleep(0.3)
    return pd.DataFrame(out)

peaks = [180.063, 166.086, 90.055]   # glucose, phenylalanine, alanine
df_ann = annotate_peaks(peaks)
print(df_ann.head(10).to_string(index=False))
df_ann.to_csv("ms_annotations.csv", index=False)

Workflow 3: Find Studies Detecting a Metabolite

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

def studies_with(refmet_name, enrich_n=20):
    """Return a DataFrame: study_id rows that report the metabolite, enriched with
    title + species for the first `enrich_n` IDs (via study/study_id/.../summary)."""
    r = requests.get(f"{BASE}/study/refmet_name/{refmet_name}/summary", timeout=60)
    r.raise_for_status()
    d = r.json()
    rows = list(d.values()) if isinstance(d, dict) else d
    ids = sorted({row["study_id"] for row in rows if row.get("study_id")})
    enriched = []
    for sid in ids[:enrich_n]:
        enriched.append(requests.get(
            f"{BASE}/study/study_id/{sid}/summary", timeout=30).json())
    return pd.DataFrame(enriched)

df = studies_with("Glucose", enrich_n=20)
print(f"Glucose-detecting studies (first 20 enriched): {len(df)}")
print(df.groupby("species").size().sort_values(ascending=False).head(8))

Key Parameters

ParameterEndpointDefaultRange / OptionsEffect
contextpathrequiredcompound, refmet, moverz, study, analysis, metabolite, gene, proteinAPI context selector
input_itempathrequireddepends on context (see "Allowed input_item Values per Context")Identifier type
input_valuepathrequiredstringThe actual identifier or value
output_itempathallall, summary, metabolites, factors, data, etc.What aspect to return
formatpath(varies)json, txtmoverz only emits txt; do NOT append /json to study/.../summary
mz / ion / tolerancemoverz pathrequiredfloat / M+H, M-H, M+Na, M+K, etc. / floatMass tolerance in Da

Best Practices

  1. Use refmet/match first for free-text input. compound/name/... is rejected by the server (name is not an allowed input_item).
  2. moverz is TSV-only. Parse with pd.read_csv(io.StringIO(r.text), sep="\t") — never call .json() on the response.
  3. Don't append /json to study/.../summary. The default is JSON; the suffix flips the response to TSV.
  4. refmet/name/{x}/all needs the canonical RefMet name. If you have user text, run it through refmet/match first.
  5. Compound results paged by formula come keyed '1','2',... — iterate dict.values() or pass to pd.DataFrame.from_dict(orient="index").
  6. Always time.sleep(0.3) in batch loops — no rate limit is published but the server is shared.

Common Recipes

Recipe: Cross-Database ID Mapping (PubChem ↔ KEGG ↔ HMDB)

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"

def cross_refs(refmet_name):
    rm = requests.get(f"{BASE}/refmet/name/{refmet_name}/all", timeout=30).json()
    if not isinstance(rm, dict) or not rm:
        return None
    cid = rm.get("pubchem_cid")
    if not cid:
        return {"refmet": refmet_name, "pubchem_cid": None}
    c = requests.get(f"{BASE}/compound/pubchem_cid/{cid}/all/json", timeout=30).json()
    return {"refmet": refmet_name,
            "pubchem_cid": cid,
            "kegg_id": c.get("kegg_id"),
            "hmdb_id": c.get("hmdb_id"),
            "inchi_key": rm.get("inchi_key")}

df = pd.DataFrame([cross_refs(n) for n in ["Glucose", "L-Tyrosine", "Cholesterol"]])
print(df.to_string(index=False))

Recipe: Pull a Study's Metabolite Table

import requests, pandas as pd

BASE = "https://www.metabolomicsworkbench.org/rest"
r = requests.get(f"{BASE}/study/study_id/ST000001/metabolites", timeout=60)
r.raise_for_status()
rows = list(r.json().values())
df = pd.DataFrame(rows)
print(f"ST000001 metabolites: {len(df)}")
print(df[["analysis_id", "analysis_summary", "metabolite_name", "refmet_name"]].head(5).to_string(index=False))

Recipe: Gene → Metabolomics Pathways

import requests

BASE = "https://www.metabolomicsworkbench.org/rest"
g = requests.get(f"{BASE}/gene/gene_symbol/HMGCR/all", timeout=30).json()
print({k: g.get(k) for k in ["gene_symbol", "gene_id", "mgp_id",
                              "gene_name", "gene_synonyms"]})

Troubleshooting

ProblemCauseSolution
"This input item (name) is not allowed..."compound/name/... is rejectedUse one of the allowed input_item values (pubchem_cid, kegg_id, inchi_key, hmdb_id, etc.); for free text, go through refmet/match/{x} first
JSONDecodeError on moverz responsemoverz returns TSV text, not JSONParse with pd.read_csv(io.StringIO(r.text), sep="\t")
Empty list from refmet/name/{x}/allNeed the canonical RefMet name (case-sensitive)Normalise via refmet/match/{user_text} first, then plug refmet_name into refmet/name/.../all
metstat/filter/... returns []Endpoint syntax is non-functionalUse `study/{refmet_name
study/.../summary returns TSV instead of JSONThe /json suffix flips to TSVDrop the trailing /json — JSON is the default
Compound query by formula returns a dict, not a listServer pages multiple matches as {'1': {...}, '2': {...}}Iterate dict.values() (or pd.DataFrame.from_dict(d, orient='index'))
refmet/match response lacks pubchem_cidmatch returns the lightweight recordUse refmet/name/{refmet_name}/all for the full record

Related Skills

  • hmdb-database — Local HMDB XML (220K metabolites, NMR/MS spectra, disease links) for offline queries
  • pubchem-compound-search — General compound property lookups (110M+ compounds) via PubChemPy
  • kegg-database — Pathway and orthology data complementary to MW's study/metabolite hits
  • chembl-database-bioactivity — Bioactivity data for the same compounds

References

Reviews

No reviews yet. Tell others what you thought.

Comments

No login needed. Share how it worked for you, ask a question, or note where it did not run.

No comments yet. Be the first to write one.

Comments are published right away. Do not include personal information such as email addresses or phone numbers. Up to 2 URLs.

0 / 1,000 characters

This form is protected by reCAPTCHA, and the Google Privacy Policy and Terms of Service apply.

More skills from this repository

API + Python SDK for ordering cell-free protein expression and binding assays. Submit sequences for expression (10–100 µg), measure binding affinity (KD) against targets, track status, and retrieve results programmatically — no wet-lab setup. Built for ML-guided directed evolution and antibody/nanobody optimization. Requires Adaptyv account and API key.

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

aeon

Free

scikit-learn compatible Python toolkit for time series ML: classify, cluster, regress, segment, transform with 30+ algorithms (ROCKET, InceptionTime, KNN-DTW, HIVE-COTE, WEASEL). Handles panel, multivariate, and unequal-length series. Maintained successor to sktime. Alternatives: sktime (larger ecosystem), tslearn (fewer algorithms), catch22 (features only).

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

AiZynthFinder retrosynthetic route planning (CASP) from AstraZeneca Molecular AI. Monte Carlo tree search guided by a template-based neural expansion policy recursively disconnects a target SMILES until precursors are found in a purchasable stock. Covers config.yml (v4 format), aizynthcli batch screening, the AiZynthFinder/AiZynthExpander Python API, one-step disconnections, custom stocks via smiles2stock, scorers, Retro*/breadth-first/DFPN search alternatives, and reading output.json.gz / trees.json. Use for synthesis route planning, synthesizability screening, and building-block/precursor search. For reaction barriers use neb-irc-activation-energy; for 2D reaction scheme drawing use rdkit-chemdraw-cdxml.

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

Access AlphaFold DB's 200M+ predicted structures by UniProt ID. Download PDB/mmCIF, analyze pLDDT/PAE, bulk-fetch proteomes via Google Cloud. For experimental structures use PDB; for prediction use ColabFold or ESMFold.

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

Annotated matrices for single-cell genomics. Stores X with obs/var metadata, layers, embeddings (obsm/varm), graphs (obsp/varp), uns. Use for .h5ad/.zarr I/O, concatenation, scverse integration. For analysis use scanpy; for probabilistic models use scvi-tools.

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

GRN inference from expression via GRNBoost2 (gradient boosting) or GENIE3 (Random Forest). Load matrix, filter by TFs, infer TF-target-importance links, save network. Dask-parallelized to single-cell scale. Core SCENIC component.

The English summary is being prepared. Showing the original description.

jaechang-hits/SciAgent-Skills380Updated Oct 16, 2026

See all skills by jaechang-hits

Report a problem with this skill