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Divergent mutational processes distinguish hypoxic and normoxic tumours
PCAWG Consortium
McDonnell Genome Institute (MGI)
Department of Genetics
Division of Oncology
Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
DBBS - Cancer Biology
DBBS - Computational and Systems Biology
DBBS - Developmental, Regenerative and Stem Cell Biology
DBBS - Molecular Genetics and Genomics
Section of Computational Biology
Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
Siteman Cancer Center
Section of Medical Oncology
DBBS - Human and Statistical Genetics
Institute of Clinical and Translational Sciences (ICTS)
Rheumatic Diseases Research Resource-Based Center
DBBS - Immunology
Section of Stem Cell Biology
Section of Bone Marrow Transplant & Leukemia
Division of Gynecologic Oncology
Research output
:
Contribution to journal
›
Article
›
peer-review
88
Scopus citations
Overview
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Keyphrases
Tumor
100%
Hypoxia
100%
Normoxic
100%
Mutational Processes
100%
Cancer Types
40%
Hypoxic Tumors
40%
Driver Genes
20%
Primary Tumor
20%
Tumor Subtype
20%
Genomic Landscape
20%
Whole Genome
20%
Tumor Hypoxia
20%
Unknown Etiology
20%
Tumor Protein p53 (TP53)
20%
Whole-genome Sequence Data
20%
Gene Level
20%
Pan-cancer
20%
Driver mutations
20%
Gene Feature
20%
Pan-cancer Analysis
20%
Mutational Signatures
20%
Hypoxia Tumor
20%
Evolutionary Trajectory
20%
Molecular Oxygen
20%
Evolutionary Distinctiveness
20%
Mutational Load
20%
Evolutionary Landscape
20%
Non-coding Drivers
20%
Biochemistry, Genetics and Molecular Biology
Evolution
100%
Pan-cancer
66%
Whole Genome Sequencing
33%
Mutational Load
33%
Tumor Hypoxia
33%
Genomics
33%