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Datasets/BEATAML1.0-COHORT

Functional Genomic Landscape of Acute Myeloid Leukemia

MixedMachine-extracted
BEATAML1.0Available from GDC

Can it answer your research question?

2 of 6 supported
  • Overall survival

    Limited

    Vital status is informative for 85% of cases, but too few events or no time to event.API

  • Progression or recurrence

    Supported

    progression_or_recurrence is informative for 95% of cases.API

  • Treatment response

    Not supported

    treatment_outcome is populated for no case in the harmonized records.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 no case in the harmonized records.API

  • Analysis by race or ethnicity

    Supported

    Race is informative for 64% 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
CasesAPI
826
Measurement types
5
16,794 files, 39 TB
Follow-upAPI
None recorded
no survival endpoint
Treatment responseAPI
Not recorded

SubjectCALC

Myeloid

As filed by the repository

Myeloid LeukemiasLeukemias, NOSUnknownChronic Myeloproliferative DisordersPlasma Cell TumorsMyelodysplastic SyndromesHematopoietic and reticuloendothelial systems

Who is in the cohortAPI

A usable value“Not reported” or “unknown”No value recorded
  • Sex448 male · 354 female · 24 unknown
  • Race478 white · 23 black or african american · 15 asian · 13 3 other · 294 unknown · 3 not reported
  • Ethnicity406 not hispanic or latino · 39 hispanic or latino · 381 unknown
  • Vital status452 dead · 249 alive · 125 unknown

Age at diagnosis

Median 62, middle half 49–71, range 0–88 years across 779 cases.

What was measured, and on how many

5 measurement types, none covering the whole cohort.

  • Whole exome sequencing534 of 826 · 65%
  • Targeted DNA panel sequencing264 of 826 · 32%
  • Bulk RNA sequencing653 of 826 · 79%
  • Single-cell RNA sequencing8 of 826 · <1%
  • Structural Variation653 of 826 · 79%
Platform, files and data levels
AssayPlatformFilesLevels
Whole exome sequencingAPIillumina7,478-
Targeted DNA panel sequencingAPIillumina2,653-
Bulk RNA sequencingAPIillumina6,615-
Single-cell RNA sequencingAPIillumina48-
Structural VariationAPI-2,940-
How complete all 29 clinical fields are - 6 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

  • Progression or recurrenceAPI95%
  • Vital statusAPI85%
  • Cause of deathAPI0%
  • Last known disease statusAPI0%

Follow-up

  • Disease response at follow-upAPI0%
  • Progression at follow-upAPI0%
  • ECOG performance statusAPI0%

Treatment

  • Prior treatmentAPI0%
  • Treatment typeAPI0%
  • Treatment givenAPI0%
  • Therapeutic agentsAPI0%
  • Treatment outcomeAPI0%
  • Regimen or line of therapyAPI0%

Staging

  • AJCC pathologic stageAPI0%
  • AJCC clinical stageAPI0%

Diagnosis

  • Tissue or organ of originAPI100%
  • Primary diagnosisAPI96%
  • Prior malignancyAPI0%
  • Synchronous malignancyAPI0%

Pathology

  • Morphology (ICD-O)API96%
  • Tumor gradeAPI0%
  • Classification of tumorAPI0%

Demographics

  • Sex at birthAPI97%
  • RaceAPI64%
  • EthnicityAPI54%
  • Population groupAPI0%
  • Country of residenceAPI0%

Exposure

  • Tobacco smoking statusAPI0%
  • Alcohol historyAPI0%

Access

MixedSome components are open; others need approval.

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

Open components
1,276 open-access files
Controlled components
15,518 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
22
accession in the methods section
Declared using it
21
named in a data availability statement
Cited the paper
1,161
attention to the publication, not reuse of the data
Against expectation
Somewhat below
about 40 articles expected; index -0.82

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 paper1,161
  • Mentioned the dataset1
  • Accession found in text27
  • Declared using it21
  • Analyzed the data22

Against comparable datasets

22 articles analyzed these data. About 40 would be expected. The expectation comes from a model of size, age, breadth and access tier.

  • Analyzed it22
  • Expected~40
Well known, little used
The publication has 1,161 citations, about 53 for every article that analyzed the data. The finding travelled further than the resource did.
Reuse assessment
  • Reuse is within the expected range for comparable datasets (index -0.82).

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

Original publication

Articles that analyzed the data

Examples, not the full list. 47 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 5 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 = "BEATAML1.0-COHORT"
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": ["BEATAML1.0-COHORT"]}}
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("BEATAML1.0-COHORT_clinical.tsv", "w").write(tsv)
This page as data: limitations firstbash
curl -s https://cd2s.vercel.app/data/datasets/gdc-beataml1.0-cohort.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/BEATAML1.0-COHORT

    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

    1,276 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

    15,518 controlled-access files require an approved data access request. The request starts at dbGaP, not in the portal. The relevant study is phs001657.

    Requires: eRA Commons account, institutional signing official approval, dbGaP data access request for phs001657

    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=phs001657

    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":["BEATAML1.0-COHORT"]}}' \
      --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 2018
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

  • U54CA224019Architecture and Trajectory of Acquired Resistance to Therapy in AMLBRIAN J DRUKER, Shannon K. McWeeneyFY2017-2026API
  • U01CA217862Functional Genomic Discovery of Pathway Targeted and Immune Modulatory Therapeutic Combinations in Hematologic MalignanciesBRIAN J DRUKER, Jeffrey Wallace TynerFY2017-2021API
  • R01CA214428An Academic-Industry Partnership to Advance Functional Genomics for Personalized Oncology.CHRISTOPHER J KEMPFY2018-2022API
  • R01CA183974Pathogenetic Mechanism and Clinical Targeting of CSF3R-Driven CancerJeffrey Wallace TynerFY2014-2018API
  • R00CA237630Characterizing the pathogenesis and targeted therapeutics of Wilms' Tumor 1 (WT1) mutations in AMLHaijiao ZhangFY2021-2023API
  • P30CA069533Translational Oncology Research ProgramJeffrey Wallace Tyner, Mindy RobertsFY2019-2026API
  • K99CA237630Characterizing the pathogenesis and targeted therapeutics of Wilms' Tumor 1 (WT1) mutations in AMLHaijiao ZhangFY2019-2020API

Funded reuse of these data

  • R01CA225231Identification of therapeutic targets for leukemia stem cells in AML-iPSC modelsMichael Kharas, Eirini PapapetrouFY2018-2022API
  • R01CA193842Characterizing the MSI2 network in leukemiaMichael KharasFY2015-2025API
  • R01CA186702Mechanisms of epitranscriptomic regulation in cancerSAMIE R JAFFREY, Michael KharasFY2014-2026API
  • R01CA166835Targeted therapy for t(8;21)+ AMLStephen D. NimerFY2012-2026API
  • R01CA249002Fibroblast Heterogeneity in Pancreatic CancerDavid A TuvesonFY2021-2025API
  • R01CA229699Targeting aberrant enhancer landscapes in pancreatic cancerChristopher VakocFY2019-2025API
  • R01CA188134Nrf2 Regulation of Ductal Pancreatic Cancer Etiology and Treatment ResponseDavid A TuvesonFY2017-2021API
  • P20CA1929962/2 Partnership to Study Racial/Ethnic Differences in GI Cancer BiologyWilliam Richard McCombie, David A TuvesonFY2015-2018API
  • R01CA275007Therapeutic targeting of IRAK4 in MDSDaniel Starczynowski, Amit K. VermaFY2022-2026API
  • R01CA253981Modeling myelodysplasiaH. LEIGHTON GRIMES, Stephanie HaleneFY2021-2025API

and 7 more

Funded infrastructure or harmonization

  • U24CA196172ECOG-ACRIN Biospecimen Bank to Support NCTNSTANLEY R. HAMILTON, Scott D JewellFY2015-2026API
  • U10CA180899Children's Oncology Group Statistics and Data CenterTODD A ALONZO, Meenakshi DevidasFY2014-2026API
  • U10CA180888SWOG Network Group Operations Center of the NCTNDAWN HERSHMAN, PRIMO N. LARAFY2014-2026API
  • U10CA180886COG NCTN Network Group Operations CenterDouglas S. Hawkins, Richard AplencFY2014-2026API
  • U10CA180820Member Site CorePeter J ODwyer, MITCHELL D. SCHNALLFY2014-2026API
  • U10CA180794ECOG-ACRIN Network Group Statistics and Data Management CenterPAUL J CATALANO, CONSTANTINE A. GATSONISFY2014-2026API
  • P30CA008748Antitumor AssessmentElisa de Stanchina, FRANCESCA M GANYFY1985-2026API
  • P30CA240139Behavioral and Community-Based Research Shared ResourceOlveen Carrasquillo, David Benner LombardFY2019-2026API
  • U01CA224013CSHL-JAX Patient-Derived Models of Pancreatic Cancer as Systems for Investigating Tumor HeterogeneityPaul Robson, David A TuvesonFY2018-2022API
  • U01CA210240Pancreatic Cancer Detection ConsortiumMichael A. HollingsworthFY2017-2026API

and 6 more

For softwarerecord JSON