CPTAC-Breast, Colon, Ovary
Can it answer your research question?
2 of 6 supportedOverall survival
Not supportedVital status is recorded for every case and informative for none.API
Progression or recurrence
Not supportedprogression_or_recurrenceis informative for no case in the harmonized records.APITreatment response
Not supportedtreatment_outcomeis populated for no case in the harmonized records.APIWhich drug was given
Not supportedtherapeutic_agentsis recorded for no case in the harmonized records.APIStage-adjusted modelling
Supportedajcc_pathologic_stageis informative for 65% of cases.APIAnalysis by race or ethnicity
SupportedRace is informative for 97% 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
- Sex287 female · 43 male · 12 unknown
- Race254 white · 44 asian · 31 black or african american · 2 1 other · 11 not reported
- Ethnicity297 not hispanic or latino · 13 hispanic or latino · 32 not reported
- Vital status342 not reported
Age at diagnosis
What was measured, and on how many
- Whole exome sequencing340 of 342 · >99%
- microRNA sequencing310 of 342 · 91%
- Bulk RNA sequencing340 of 342 · >99%
- Structural Variation340 of 342 · >99%
How complete all 29 clinical fields are - 7 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
- 1,288 open-access files
- Controlled components
- 7,956 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
- Mentioned the dataset2
- Accession found in text8
- Declared using it6
- Analyzed the data8
Against comparable datasets
- Analyzed it8
- Expected~12
METHODS:"phs000892"), so every dataset in the corpus is counted the same way and the numbers can be compared. The 10 articles listed below were retrieved and graded one at a time, and an article counts as having analyzed the data wherever the accession sits in the analysis - methods, results, tables, figures or supplement - under any of this dataset’s accessions. Read the list as the evidence about these articles, and the count as the number that is comparable across datasets.- Reuse is within the expected range for comparable datasets (index -0.56).
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 = "CPTAC-2"
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": ["CPTAC-2"]}}
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("CPTAC-2_clinical.tsv", "w").write(tsv)This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-cptac-2.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/CPTAC-2 - Download the open files without an accountFor people
1,288 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
7,956 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000892.
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=phs000892gdc-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":["CPTAC-2"]}}' \ --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.
Versions and verification
- Released
- 1 Jan 2020
- Metadata retrieved
- 18 Sept 2026
- Review status
- Machine-extracted
- Data generation funding
- Funded data generation
Funding
Funded reuse of these data
- T32CA203690Translational Breast Cancer Research Training ProgramSuzanne AW Fuqua, Mothaffar Fahed RimawiAPI
- R50CA211499A proteomics research specialist in developing targeted mass spectrometry methods for quantifying proteins important in cancerJeff WhiteakerAPI
- R33CA173300Advanced development of immuno-MRM technology to analyze archived cancer tissuesAMANDA G PAULOVICHAPI
- R01CA235575Clinical translation of a NexGen platform for quantifying protein networks in human biospecimensAMANDA G PAULOVICHAPI
- F32CA246894Top-down proteomic characterization of MEK/ERK in MAPK-driven cancersBryon Shane DrownAPI
Funded infrastructure or harmonization
- U24CA210986Center of Excellence for High Throughput Proteogenomic CharacterizationSTEVEN A CARR, MICHAEL A GILLETTEAPI
- U24CA210979Integrated high throughput proteogenomic data analysis center for CPTACChet Birger, GAD A GETZAPI
- U24CA210972Proteogenomic Data Analysis for Cancer Systems Biology and Clinical TranslationLi Ding, David FenyoAPI
- U24CA210955PNNL Proteome Characterization CenterTao Liu, RICHARD D SMITHAPI
- U24CA210954iPGDAC, An Integrative Proteogenomic Data Analysis Center for CPTACBing ZhangAPI
- U24CA160034Proteo-genomic Discovery, Prioritization and Verification of Cancer BiomarkersSTEVEN A CARR, AMANDA G PAULOVICHAPI
- U01CA214125MICROSCALED PROTEOGENOMICS FOR CANCER CLINICAL TRIALSMeenakshi Anurag, STEVEN A CARRAPI
- U24CA160036Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchDANIEL Wanyui CHAN, ZHEN ZHANGAPI
- U24CA160019PNNL Clinical Proteome Characterization CenterKarin D Rodland, RICHARD D SMITHAPI
- U01CA214114Proteogenomic studies aimed at understanding ovarian tumor responses to agents targeting the DNA damage response and translating this knowledge into clinical benefitMichael Birrer, AMANDA G PAULOVICHAPI