Cancer Cell Line Encyclopedia (Broad, 2019)
Cancer Cell Line Encyclopedia from the Broad Institute and Novartis, updated 2019. Data downloaded from the Broad CCLE Portal. For more info about the proteomics data, see the README.
Can it answer your research question?
1 of 6 supportedOverall survival
Not supportedNo usable overall-survival endpoint: vital status or follow-up time is missing.API
Progression or recurrence
Not measuredThis field was not among those probed for this repository.
Treatment response
Not supportedNo treatment response is recorded in the harmonized records.API
Which drug was given
Not measuredThis field was not among those probed for this repository.
Stage-adjusted modelling
Not measuredThis field was not among those probed for this repository.
Analysis by race or ethnicity
SupportedETHNICITY is informative for 60% 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
- Sex508 Male · 407 Female · 824 no value recorded
- Race359 Caucasian · 181 Asian · 33 African_American · 6 5 other · 1,160 no value recorded
- Ethnicity670 Caucasian · 306 Asian · 61 African_american · 702 no value recorded
What was measured, and on how many
- Mutation calls (panel, exome or genome)1,570 of 1,739 samples · 90%
- Copy number alterations1,030 of 1,739 samples · 59%
- RNA sequencing expression1,156 of 1,739 samples · 66%
- Mass spectrometry proteomics375 of 1,739 samples · 22%
- Structural variants / fusions
How complete all 5 clinical fields are - 1 informative for at least 80% of cases
Access
Processed data download from the cBioPortal study page or its public REST API; no account required. Primary raw data remain wherever the original investigators deposited them.
- Open components
- harmonized mutation, copy-number, expression and clinical files
- License
- Per-study terms; cBioPortal asks that the original study be cited
- Citation requirement
- Cite the original publication, and cite cBioPortal if the portal's harmonized files were used.
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.
- Not assessed: this dataset has no accession specific enough for citation-based reuse tracing, so a shortfall cannot be measured.
Original publication
Articles that analyzed the data
Not searchable. See the note above.
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
cBioPortal: clinical data and the full study bundlepython
import requests, pandas as pd
STUDY = "ccle_broad_2019"
base = "https://www.cbioportal.org/api"
clin = requests.get(f"{base}/studies/{STUDY}/clinical-data",
params={"clinicalDataType": "PATIENT", "projection": "SUMMARY"}, timeout=60).json()
patients = pd.DataFrame(clin).pivot_table(index="patientId", columns="clinicalAttributeId",
values="value", aggfunc="first")
print(patients.shape)
profiles = requests.get(f"{base}/studies/{STUDY}/molecular-profiles", timeout=60).json()
print([p["molecularProfileId"] for p in profiles])
# Whole study as flat files: https://cbioportal-datahub.s3.amazonaws.com/ccle_broad_2019.tar.gzThis page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/cbio-ccle-broad-2019.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 study in cBioPortalFor people
Harmonized molecular and clinical files are open. Cite the original publication, and cite cBioPortal if the portal's harmonized files were used.
https://www.cbioportal.org/study/summary?id=ccle_broad_2019 - Download the whole study as a zipFor people
The datasets page carries the staging files used by the portal.
https://www.cbioportal.org/datasets - Or pull the staging files with git-lfsFor people
Study folders are named by study id under public/.
https://github.com/cBioPortal/datahubgit clone https://github.com/cBioPortal/datahub.git && cd datahub git -c lfs.fetchexclude="" lfs pull -I public/ccle_broad_2019 - Read the study straight from the REST APIFor agents
No key is required; pace requests when sweeping many studies.
https://docs.cbioportal.org/web-api-and-clients/curl -s 'https://www.cbioportal.org/api/studies/ccle_broad_2019/clinical-data?clinicalDataType=PATIENT&projection=SUMMARY'
Provenance
All of it, and more, is in this record’s JSON.
Identifiers
- cBioPortal studyccle_broad_2019API
Versions and verification
- Metadata retrieved
- 18 Sept 2026
- Review status
- Machine-extracted
- Data generation funding
- Funded data generation
Funding
Funded data generation
- U54CA224068An integrated translational approach to overcome drug resistanceRyan Bruce Corcoran, KEITH T FLAHERTYAPI
- U24CA210950Integrated analysis of protein expression data from the Reverse Phase Protein Array (RPPA) platformRehan Akbani, GORDON B. MILLSAPI
- U24CA210949Batch effects in molecular profiling data on cancers: detection, quantitation, interpretation, and correctionRehan Akbani, GORDON B. MILLSAPI
- U24CA180922Trinity: Transcriptome assembly for genetic and functional analysis of cancerBrian Haas, Eric BanksAPI
- U01CA217842Integrative bioinformatics and functional characterization of oncogenic driver aberrations in cancerBenjamin Deneen, GORDON B. MILLSAPI
- U01CA176058The Dana-Farber Cancer Institute Cancer Target Discovery and Development CenterWilliam C. Hahn, TODD R. GOLUBAPI
- R50CA221675Functional Proteomics by Reverse Phase Protein Array in CancerYILING LUAPI
- R50CA211461Open Software and Resource Development Leveraging Next-gen Sequencing Data to Facilitate Computational Analysis of Cancer BiologyBrian HaasAPI
- R37CA225191Targeting blastic plasmacytoid dendritic cell neoplasm (BPDCN)Andrew A LaneAPI
- R01CA219943Characterizing TP53 and PPM1D mutations as resistance drivers to radiation therapy in Diffuse Intrinsic Pontine GliomasRAMEEN BEROUKHIM, KEITH LLOYD LIGONAPI