Stomach Adenocarcinoma
The Cancer Genome Atlas-Stomach Adenoarcinoma (TCGA-STAD) data collection is part of a larger effort to enhance the TCGA data set with characterized radiological images. The Cancer Imaging Program (CIP) with the cooperation of several of the TCGA tissue-contributing institutions are working to archive a large portion of the radiological images of the genetically-analyzed STAD cases. Please see the TCGA-STAD page to learn more about the radiology images and to obtain any supporting metadata for this collection. Please see the DICOM converted Slide Microscopy images for the TCGA-STAD collection page to learn more about the histopathology images and to obtain any supporting metadata for this collection.
Can it answer your research question?
6 of 6 supportedOverall survival
SupportedVital status and time are populated; median follow-up 1.2 years; 440 cases with follow-up; endpoints: overall survival, progression-free interval.API
Progression or recurrence
SupportedA time to event is derivable: progression-free interval;
progression_or_recurrenceis informative for 26% of cases.APITreatment response
Supporteddisease_responseis populated for 92% of cases; criteria: complete response, partial response.APIWhich drug was given
Supportedtherapeutic_agentsis recorded for 43% of cases.APIStage-adjusted modelling
Supportedajcc_pathologic_stageis informative for 94% of cases.APIAnalysis by race or ethnicity
SupportedRace is informative for 86% of cases.API
At a glance
Every percentage is the repository’s own record of what is filled inSubjectCALC
As filed by the repository
Who is in the cohortAPI
- Sex285 male · 158 female
- Race278 white · 89 asian · 13 black or african american · 1 1 other · 50 not reported · 12 unknown
- Ethnicity318 not hispanic or latino · 5 hispanic or latino · 115 not reported · 5 unknown
- Vital status268 alive · 175 dead
Age at diagnosis
What was measured, and on how many
- Whole exome sequencing443 of 443 · 100%
- SNP genotyping array (copy number, germline)443 of 443 · 100%
- DNA methylation array443 of 443 · 100%
- Clinical443 of 443 · 100%
- DICOM medical imaging443 of 443 · 100%
- microRNA sequencing436 of 443 · 98%
- Whole genome sequencing436 of 443 · 98%
- Somatic Structural Variation430 of 443 · 97%
- Whole-slide diagnostic images416 of 443 · 94%
- Bulk RNA sequencing415 of 443 · 94%
- Reverse phase protein array357 of 443 · 81%
- ATAC sequencing (chromatin accessibility)21 of 443 · 5%
Platform, files and data levels
| Assay | Platform | Files | Levels |
|---|---|---|---|
| Whole exome sequencingAPI | illumina | 7,086 | - |
| SNP genotyping array (copy number, germline)API | illumina | 5,846 | - |
| DNA methylation arrayAPI | illumina | 1,410 | - |
| ClinicalAPI2 | - | 906 | - |
| DICOM medical imagingAPI | - | - | DICOM series |
| microRNA sequencingAPI | illumina | 1,473 | - |
| Whole genome sequencingAPI2 | illumina | 7,936 | - |
| Somatic Structural VariationAPI | - | 1,789 | - |
| Whole-slide diagnostic imagesAPI2 | illumina | 442 | - |
| Bulk RNA sequencingAPI | illumina | 4,032 | - |
| Reverse phase protein arrayAPI | illumina | 357 | - |
| ATAC sequencing (chromatin accessibility)API | illumina | 21 | - |
How complete all 29 clinical fields are - 16 informative for at least 80% of cases
Outcome
Follow-up
Treatment
Diagnosis
Demographics
Access
Data Access Request through dbGaP using an eRA Commons account; institutional signing official approval required
- Open components
- 11,791 open-access files
- Controlled components
- 19,813 controlled-access files
- Typical turnaround
- days to a few weeks after signing official approval
- License
- NIH Genomic Data Sharing Policy terms
- Citation requirement
- Cite the dataset accession and the program's publication guidelines; see the GDC publication policy.
What it is good for
Written and checked by a reviewer, not generated from metadata.
No reviewed research questions yet. The measurements and field completeness above are machine-extracted and still useful for judging fit.
What it cannot tell you
Written by a reviewer against the source, not inferred from what is missing.
No reviewed limitations yet. Check the field completeness chart above before committing to an analysis. Low coverage on an endpoint you need is the most common blocker.
Who has used it
Articles that analyzed these data, counted separately from articles that only cited the paper. Only the first counts as reuse.
What articles did with it
- Cited the paper5,063
- Mentioned the dataset112
- Accession found in text0
- Declared using it143
- Analyzed the data1,405
Against comparable datasets
- Analyzed it1,405
- Expected~293
- Reuse is within the expected range for comparable datasets (index +2.26).
Original publication
Articles that analyzed the data
Community examples
Share your exampleAnalyses someone ran on these data end to end, each with a receipt recording when it ran, against which packages and for how long.
Nobody has shared an analysis of this dataset yet. The examples on other datasets cover the common patterns and can be adapted - and if you adapt one, it belongs here.
Start here
Starter code generated from this record’s own identifiers, then the access steps.
Get the data in code
GDC: list open files and download thempython
import json, requests
PROJECT = "TCGA-STAD"
filters = {"op": "and", "content": [
{"op": "in", "content": {"field": "cases.project.project_id", "value": [PROJECT]}},
{"op": "in", "content": {"field": "access", "value": ["open"]}},
]}
params = {"filters": json.dumps(filters),
"fields": "file_id,file_name,data_category,data_type,file_size",
"size": "10000", "format": "JSON"}
files = requests.get("https://api.gdc.cancer.gov/files", params=params, timeout=60).json()["data"]["hits"]
print(len(files), "open files")
# Write a manifest and fetch with the GDC client (https://gdc.cancer.gov/access-data/gdc-data-transfer-tool)
with open("manifest.txt", "w") as fh:
fh.write("id\n" + "\n".join(f["file_id"] for f in files))
# $ gdc-client download -m manifest.txtGDC: clinical table for every casepython
import json, requests
filters = {"op": "in", "content": {"field": "project.project_id", "value": ["TCGA-STAD"]}}
params = {"filters": json.dumps(filters), "size": "5000", "format": "TSV",
"fields": ",".join([
"submitter_id", "demographic.vital_status", "demographic.days_to_death",
"diagnoses.days_to_last_follow_up", "diagnoses.ajcc_pathologic_stage",
"diagnoses.treatments.treatment_type", "diagnoses.treatments.treatment_outcome"])}
tsv = requests.get("https://api.gdc.cancer.gov/cases", params=params, timeout=60).text
open("TCGA-STAD_clinical.tsv", "w").write(tsv)IDC: pull the DICOM collection with idc-indexpython
from idc_index import IDCClient
COLLECTION = "tcga_stad"
client = IDCClient()
series = client.index[client.index["collection_id"] == COLLECTION] # one row per DICOM series
print(len(series), "series,", series["PatientID"].nunique(), "patients,",
round(series["series_size_MB"].sum() / 1024, 1), "GB")
print(series["Modality"].value_counts().to_dict())
# Everything above is an index lookup and costs nothing. Uncomment to pull the pixels;
# the client refuses up front if the disk cannot hold them.
# client.download_from_selection(collection_id=COLLECTION, downloadDir="./tcga_stad")This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-tcga-stad.json | python3 -c '
import json, sys
r = json.load(sys.stdin)
for l in r["limitations"]:
print(l["severity"].upper(), "-", l["statement"][:120])
print("survival endpoint:", r["longitudinal"]["has_survival_endpoint"], "| treatment response:", r["longitudinal"]["has_treatment_response"])'Access steps
- Open the project in the GDC Data PortalFor people
Check the portal's current case and file counts before requesting anything; the cohort can change after this record was built.
https://portal.gdc.cancer.gov/projects/TCGA-STAD - Download the open files without an accountFor people
11,791 open-access files are marked open access. Add them to a portal cart, export a manifest, and fetch it with the GDC Data Transfer Tool.
https://gdc.cancer.gov/access-data/gdc-data-transfer-toolgdc-client download -m gdc_manifest.txt - Request controlled access through dbGaPFor people
19,813 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000178.
https://gdc.cancer.gov/access-data/obtaining-access-controlled-data - Download controlled files with your tokenFor people
An approved request yields a token. The same manifest fetches nothing controlled without it.
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000178gdc-client download -m gdc_manifest.txt -t gdc-user-token.txt - Query the project from code, with no credentialsFor agents
The file index is public even where files are not, so an agent can size the cohort before anyone requests access.
https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/curl -s 'https://api.gdc.cancer.gov/files' --get \ --data-urlencode 'filters={"op":"in","content":{"field":"cases.project.project_id","value":["TCGA-STAD"]}}' \ --data-urlencode 'fields=file_id,file_name,data_type' \ --data-urlencode 'size=10000' --data-urlencode 'format=TSV' - Pass the token when the agent needs controlled filesFor agents
Without a token, an API query may return only the open subset. Compare returned counts with the record before treating them as the whole cohort.
https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/curl -H "X-Auth-Token: $GDC_TOKEN" https://api.gdc.cancer.gov/data/<file_id>
Provenance
All of it, and more, is in this record’s JSON.
Identifiers
Versions and verification
- Released
- 1 Jan 2013
- Metadata retrieved
- 18 Sept 2026
- Review status
- Machine-extracted
- Data generation funding
- Funded data generation
Funding
Funded data generation
- U24CA180951Cloud Based Resource for Data Hosting, Visualization and Analysis Using UCSC CancDAVID H HAUSSLERAPI
- U24CA144025Harvard Genome Characterization CenterRaju S. KucherlapatiAPI
- U24CA143883Integrative Pipeline for Analysis & Translational Application of TCGA Data (GDAC)Rehan Akbani, GORDON B. MILLSAPI
- U24CA143882The USC-JHU Cancer Epigenome Characterization CenterSTEPHEN B. BAYLIN, Daniel Joseph WeisenbergerAPI
- U24CA143867Genome Characterization Center (GCC)Stacey Gabriel, Matthew L. MeyersonAPI
- U24CA143866Cancer transcriptome characterization using massively parallel DNA sequencingMarco Antonio MarraAPI
- U24CA143858UCSC-Buck Inst. Genome Data Analysis Center for TCGA Research Network (GDAC)Christopher Benz, DAVID H HAUSSLERAPI
- U24CA143848Gene Expression Patterns in Human Tumors Identified Using Transcript SequencingDavid N Hayes, CHARLES M PEROUAPI
- U24CA143845The Cancer Genome Atlas Data Analysis CenterLYNDA CHIN, GAD A GETZAPI
- U24CA143843The BCM Tumor Genome Characterization CenterRICHARD A GIBBS, David Andrew WheelerAPI
Funded reuse of these data
- R01CA265026Defining the role of histone H3K4 mono-methyltransferase dysfunction in urothelial carcinomaYu ChenAPI
- R01CA228216Epigenetic mechanisms of transcriptional activation of a novel oncogenic ALK variant in cancerPing ChiAPI
- R01CA208100Understanding the role of an aberrant hepatic nuclear transcription circuit in prostate cancer tumorigenesis and castration resistanceYu ChenAPI
- R01CA193837Role of ETS factors in specifying prostate luminal cell identity and androgen receptor dependenceCHARLES L. SAWYERSAPI
Funded infrastructure or harmonization
- U54CA224079Project 2: Reversing resistance caused by lineage plasticity through epigenetic therapyYu Chen, CHARLES L. SAWYERSAPI
- U01CA224044Patient-Derived Models of Prostate Cancer for Personalized MedicineYu Chen, PHILLIP ANDREW FUTREALAPI
- P50CA221745Biospecimen Repository CoreHikmat Al-Ahmadie, David B. SolitAPI
- P50CA217694Project 3: Identifying Targetable Epigenetic and Immuno-Oncologic Vulnerabilities in Synovial SarcomaMarc Ladanyi, SAMUEL SINGERAPI
- P50CA092629SPORE in Prostate CancerYu Chen, MICHAEL J MORRISAPI
- P30CA008748Antitumor AssessmentElisa de Stanchina, FRANCESCA M GANYAPI