Research reading room
Pediatric Acute Lymphoid Leukemia - Phase II (TARGET, 2018)
Summary
Pediatric Acute Lymphoid Leukemia - Phase II (TARGET, 2018) is a study catalogued by cBioPortal DataHub under the cancer-type code bll. EvidenceHelix groups it with blood, lymph and bone marrow studies.
Study description
Whole genome or whole exome sequencing on 298 Pediatric Acute Lymphoid Leukemia - Phase II samples. Comprehensive profiling of ALL Phase 2 samples. TARGET data is intended exclusively for biomedical research using pediatric data (i.e., the research objectives cannot be accomplished using data from adults) that focus on the development of more effective treatments, diagnostic tests, or prognostic markers for childhood cancers. Moreover, TARGET data can be used for research relevant to the biology, causes, treatment and late complications of treatment of pediatric cancers, but is not intended for the sole purposes of methods and/or tool development (please see Using TARGET Data (https://ocg.cancer.gov/programs/target/using-target-data) section of the OCG website). If you are interested in using TARGET data for publication or other research purposes, you must follow the TARGET Publication Guidelines (https://ocg.cancer.gov/programs/target/target-publication-guidelines).
Text as published in the source's study metadata.
Citation & PubMed
The source lists no citation or PubMed id for this study.
Source & licence
Metadata from cBioPortal DataHub at e1b75cd25b, available under the ODC Open Database License (ODbL) 1.0. See the Source metadata tab for every field.
Source metadata
- Study identifier
- all_phase2_target_2018_pub
- Short name
- ALL-Phase II (TARGET, 2018)
- Source cancer-type code
- bll
- Reference genome
- not given
- Source access groups
- NCI-TARGET;PUBLIC
- Original study
- View on cBioPortal
- Metadata file
- meta_study.txt at e1b75cd25b
- Database licence
- ODC Open Database License (ODbL) 1.0
Study-level metadata only (title, description, cancer-type code, citation, PubMed ids). No patient, sample, mutation or clinical data, and no publication full text, is included. Individual studies may carry their own terms; follow each study's source links before reusing its data.
Citations
The source lists no citation or PubMed id for this study.
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