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Datasets/TCGA-SARC

Sarcoma

MixedMachine-extracted
TCGAAvailable from GDC and IDC

The Cancer Genome Atlas-Sarcoma Cancer (TCGA-SARC) 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 SARC cases. Please see the TCGA-SARC 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-SARC collection page to learn more about the histopathology images and to obtain any supporting metadata for this collection.

Can it answer your research question?

3 of 6 supported
  • Overall survival

    Supported

    Vital status and time are populated; median follow-up 2.6 years; 261 cases with follow-up; endpoints: overall survival, progression-free interval.API

  • Progression or recurrence

    Supported

    A time to event is derivable: progression-free interval; progression_or_recurrence is informative for 46% of cases.API

  • Treatment response

    Limited

    disease_response is populated for 100% of cases.API

  • Which drug was given

    Not supported

    therapeutic_agents is recorded for no case in the harmonized records.API

  • Stage-adjusted modelling

    Not supported

    ajcc_pathologic_stage is informative for 2% of cases.API

  • Analysis by race or ethnicity

    Supported

    Race is informative for 97% of cases.API

Judged from the repository’s own field completeness (thresholds). “Not measured” means we have not probed that field for this record, not that the data lack it.

At a glance

Every percentage is the repository’s own record of what is filled in
CasesAPI2
261
Measurement types
11
16,404 files, 130 TB
Follow-upAPI
2.6 years
for 261 of 261 cases; overall survival, progression-free interval
Treatment responseAPI
Not recorded

SubjectCALC

Soft tissue

As filed by the repository

Lipomatous NeoplasmsFibromatous NeoplasmsSynovial-like NeoplasmsMyomatous NeoplasmsNerve Sheath TumorsSoft Tissue Tumors and Sarcomas, NOSBones, joints and articular cartilage of limbsChest-Abdomen-PelvisColonConnective, subcutaneous and other soft tissuesCorpus uteriKidney

Who is in the cohortAPI

A usable value“Not reported” or “unknown”No value recorded
  • Sex142 female · 119 male
  • Race228 white · 18 black or african american · 6 asian · 6 not reported · 3 unknown
  • Ethnicity223 not hispanic or latino · 5 hispanic or latino · 20 not reported · 13 unknown
  • Vital status162 alive · 99 dead

Age at diagnosis

Median 61, middle half 53–71, range 6–90 years across 260 cases.

What was measured, and on how many

11 measurement types, 5 covering the whole cohort.

  • SNP genotyping array (copy number, germline)261 of 261 · 100%
  • DNA methylation array261 of 261 · 100%
  • Whole-slide tissue images261 of 261 · 100%
  • Clinical261 of 261 · 100%
  • DICOM medical imaging261 of 261 · 100%
  • Bulk RNA sequencing259 of 261 · >99%
  • microRNA sequencing259 of 261 · >99%
  • Whole exome sequencing255 of 261 · 98%
  • Whole genome sequencing223 of 261 · 85%
  • Reverse phase protein array223 of 261 · 85%
  • Somatic Structural Variation215 of 261 · 82%
Platform, files and data levels
AssayPlatformFilesLevels
SNP genotyping array (copy number, germline)APIillumina3,364-
DNA methylation arrayAPIillumina807-
Whole-slide tissue imagesAPI2illumina290-
ClinicalAPI2-576-
DICOM medical imagingAPI--DICOM series
Bulk RNA sequencingAPIillumina2,385-
microRNA sequencingAPIillumina789-
Whole exome sequencingAPIillumina4,101-
Whole genome sequencingAPI2illumina2,734-
Reverse phase protein arrayAPIillumina226-
Somatic Structural VariationAPI-609-
How complete all 29 clinical fields are - 13 informative for at least 80% of cases

A field counts as informative only when it holds a real value. “Not reported” blocks an analysis just as a missing field does. Fields marked 1:n can hold several records per case, so they show the share of cases with any record.

Informative - a usable valuePresent but uninformative - “not reported” or “unknown”Absent - no value recorded

Outcome

  • Vital statusAPI100%
  • Cause of deathAPI0%
  • Progression or recurrenceAPI0%
  • Last known disease statusAPI0%

Follow-up

  • Disease response at follow-up1:nAPI>99%
  • Progression at follow-upAPI46%
  • ECOG performance statusAPI0%

Treatment

  • Prior treatment1:nAPI100%
  • Treatment typeAPI14%
  • Treatment givenAPI12%
  • Therapeutic agentsAPI0%
  • Treatment outcomeAPI0%
  • Regimen or line of therapyAPI0%

Staging

  • AJCC pathologic stageAPI2%
  • AJCC clinical stageAPI0%

Diagnosis

  • Primary diagnosis1:nAPI100%
  • Tissue or organ of origin1:nAPI100%
  • Prior malignancyAPI>99%
  • Synchronous malignancyAPI>99%

Pathology

  • Morphology (ICD-O)1:nAPI100%
  • Classification of tumor1:nAPI100%
  • Tumor gradeAPI0%

Demographics

  • Sex at birthAPI100%
  • Country of residenceAPI100%
  • RaceAPI97%
  • EthnicityAPI87%
  • Population groupAPI0%

Exposure

  • Tobacco smoking statusAPI0%
  • Alcohol historyAPI0%

Access

MixedSome components are open; others need approval.API

Data Access Request through dbGaP using an eRA Commons account; institutional signing official approval required

Open components
6,613 open-access files
Controlled components
9,791 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.

Analyzed the dataCALC2
192
accession in the methods; 100% of a 29-article sample really cited it
Declared using it
30
named in a data availability statement
Cited the paper
891
attention to the publication, not reuse of the data
Against expectation
As expected or above
about 109 articles expected; index 0.81

What articles did with it

Only the last row counts as reuse. Where the accession appears in an article tells us what the authors did with the data.

  • Cited the paper891
  • Mentioned the dataset23
  • Accession found in text0
  • Declared using it30
  • Analyzed the data192

Against comparable datasets

192 articles analyzed these data. About 109 would be expected. The expectation comes from a model of size, age, breadth and access tier.

  • Analyzed it192
  • Expected~109
Reuse assessment
  • Reuse is within the expected range for comparable datasets (index +0.81).

Compared against 132 datasets in this corpus with a citable accession and sufficient metadata. See Methods for the model.

Articles that analyzed the data

Examples, not the full list. 83 articles matching this dataset's accession search were retrieved and graded individually; these are the strongest of those.

Deep-review sample: author overlap and funding were checked only for the 10 articles listed here, not for every article examined. Of the 10 that analyzed the data, 10 of the 10 we could check had no author in common with the generating team, and 2 of the 10 we could check were themselves NCI-funded. These are sample counts, not population estimates.

Community examples

Share your example

Analyses 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

Open-access files need no account. Controlled files need an approved dbGaP request and a token passed to gdc-client.

import json, requests

PROJECT = "TCGA-SARC"
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.txt
GDC: clinical table for every casepython
import json, requests

filters = {"op": "in", "content": {"field": "project.project_id", "value": ["TCGA-SARC"]}}
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-SARC_clinical.tsv", "w").write(tsv)
IDC: pull the DICOM collection with idc-indexpython

pip install idc-index. Images are public; the package uses s5cmd under the hood.

from idc_index import IDCClient

COLLECTION = "tcga_sarc"
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_sarc")
This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-tcga-sarc.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

  1. 1
    Open the project in the GDC Data PortalFor people5 minutes

    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-SARC

    Generated from repository policy. Check the linked policy before downloading.

  2. 2
    Download the open files without an accountFor peopleminutes to hours, by cohort size

    6,613 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.

    gdc-client download -m gdc_manifest.txt
    https://gdc.cancer.gov/access-data/gdc-data-transfer-tool

    Generated from repository policy. Check the linked policy before downloading.

  3. 3
    Request controlled access through dbGaPFor peopledays to a few weeks after signing official approval

    9,791 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs000178.

    Requires: eRA Commons account, institutional signing official approval, dbGaP data access request for phs000178

    https://gdc.cancer.gov/access-data/obtaining-access-controlled-data

    Generated from repository policy. Check the linked policy before downloading.

  4. 4
    Download controlled files with your tokenFor people

    An approved request yields a token. The same manifest fetches nothing controlled without it.

    Requires: approved dbGaP request, GDC authentication token

    gdc-client download -m gdc_manifest.txt -t gdc-user-token.txt
    https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000178

    Generated from repository policy. Check the linked policy before downloading.

  5. 5
    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.

    curl -s 'https://api.gdc.cancer.gov/files' --get \
      --data-urlencode 'filters={"op":"in","content":{"field":"cases.project.project_id","value":["TCGA-SARC"]}}' \
      --data-urlencode 'fields=file_id,file_name,data_type' \
      --data-urlencode 'size=10000' --data-urlencode 'format=TSV'
    https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/

    Generated from repository policy. Check the linked policy before downloading.

  6. 6
    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.

    Requires: GDC authentication token

    curl -H "X-Auth-Token: $GDC_TOKEN" https://api.gdc.cancer.gov/data/<file_id>
    https://docs.gdc.cancer.gov/API/Users_Guide/Getting_Started/

    Generated from repository policy. Check the linked policy before downloading.

Provenance

All of it, and more, is in this record’s JSON.

Identifiers

Versions and verification

Released
1 Jan 2017
Metadata retrieved
18 Sept 2026
Review status
Machine-extracted
Data generation funding
Funded data generation

Funding

Awards resolved through NIH RePORTER. Awards that paid to generate these data are listed apart from awards that paid to reuse them. Both are returns on NCI investment, but different ones.

Funded data generation

  • U24CA210999Global Infrastructure for Collaborative High-throughput Cancer Genomics AnalysisGAD A GETZFY2016-2020API
  • U24CA210990UCSC-Buck Specialized Genomic Data Analysis Center for the Genomic Data Analysis NetworkJOSHUA Michael STUARTFY2016-2020API
  • U24CA210974Visualization hub for genomics data exploration and translational discoveryEric Collisson, DAVID H HAUSSLERFY2016-2020API
  • U24CA210969Integrative Cancer Epigenomic Data Analysis Center (ICE-DAC)PETER W LAIRD, Benjamin P BermanFY2016-2020API
  • U24CA210957OHSU Center for Specialized Data Analysis as part of the GDANEmek Demir, PAUL T. SPELLMANFY2016-2020API
  • U24CA210950Integrated analysis of protein expression data from the Reverse Phase Protein Array (RPPA) platformRehan Akbani, GORDON B. MILLSFY2016-2020API
  • U24CA210949Batch effects in molecular profiling data on cancers: detection, quantitation, interpretation, and correctionRehan Akbani, GORDON B. MILLSFY2016-2020API
  • U24CA199461Next-Generation Clustered Heat Maps for fluent, interactive exploration of omic dataBradley McIntosh Broom, John N WeinsteinFY2015-2019API
  • U24CA194362Advanced Development of an Open-source Platform for Web-based Integrative Digital Image Analysis in CancerLee Cooper, David Andrew GutmanFY2015-2019API
  • U24CA144025Harvard Genome Characterization CenterRaju S. KucherlapatiFY2009-2016API

and 13 more

Funded reuse of these data

  • T32CA009071Molecular Targets for Cancer Detection and TreatmentMary Y Armanios, Nilofer S. AzadFY1985-2026API
  • R01CA229688The role and regulation of Hippo pathway in sarcomagenesisTzipora Sarah Karin eisingerFY2019-2023API
  • K08CA245181Targeting Radiation-Induced Myeloid Cells to Promote T cell Immunity in Undifferentiated Pleomorphic SarcomaAnusha KalbasiFY2020-2025API

Funded infrastructure or harmonization

  • U54CA283762PDX CoreJENNIFER E KOBLINSKI, Jose G. TrevinoFY2023-2026API
  • U54CA210173Computational CoreSEAN X SUN, Sharon GerechtFY2016-2020API
  • P30CA016520Hematologic Malignancies ProgramEdward A Stadtmauer, STEPHAN A. GRUPPFY1985-2026API

For softwarerecord JSON