-
INCLIVA-CC-panel DAC
Dac
EGAC50000000061
-
OICR-DAC, Ontario Institute for Cancer Research
Dac
EGAC00001000591
-
OICR-DAC, Ontario Institute for Cancer Research
Dac
EGAC00001000710
-
MESA colorectal cancer data access committee
Dac
EGAC00001002798
-
Exceptional Outcomes in a Phase Ib Study Combining PARP and MEK Inhibition, With or Without Anti-PD-L1, for BRCA-Wildtype Platinum-Sensitive Recurrent Ovarian Cancer
Study
EGAS00001007496
-
Converging and evolving immuno-genomic routes towards immune escape in breast cancer
Dac
EGAC50000000074
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer - Data Access Committee
Dac
EGAC00001002905
-
Cancer Epigenetics Group
Dac
EGAC00001003349
-
Netherlands Cancer Institute (NKI-AVL) general DAC
Dac
EGAC50000000055
-
Cancer Registry of Norway - NIPH Data Access Committee for CRCbiome datasets
Dac
EGAC50000000121
-
SCANDARE MACARON project
Dac
EGAC50000000104
-
Access to dataset, "Feasibility of Functional Precision Medicine for Guiding Treatment of Relapsed/Refractory Pediatric Cancers"
Dac
EGAC50000000124
-
This DAC takes care of requests for data for the Swiss epigenetic colorectal cancer cohort study, SWEPIC
Dac
EGAC00001003471
-
Division of Molecular Oncology, National Cancer Center Research Institute Data Access Committee
Dac
EGAC00001003030
-
Singapore Gastric Cancer Consortium Data Access Committee
Dac
EGAC00001003138
-
DAC for noninvasive lung cancer subtyping
Dac
EGAC00001003474
-
Ultra-deep targeted sequencing for studying the accumulation of somatic mutations in cancer-free human skin
Study
EGAS00001004279
-
Oncogenic Ectodomain deletion of FGFR1 caused by Breakage-Fusion-Bridges in Squamous Cell lung Cancer
Study
EGAS00001005059
-
Mutant p53 confers gain-of-function transcriptional activity in liver cancer
Study
EGAS00001005779
-
Unraveling the genetics of transformed splenic marginal zone lymphoma
Study
EGAS00001006389
-
Leukemia sequencing study
Study
EGAS00001006901
-
Detection of rare mutations, copy number variation, and DNA methylation in the same template DNA molecules
Study
EGAS00001006839
-
Targeted sequence of MDS cases treated with azacitidine
Study
EGAS00001007030
-
Sequencing of Ovarian Cancer
Study
EGAS00001007489
-
Sequencing of Breast Cancer
Study
EGAS00001007490
-
Lung cancer cfDNA dataset DAC
Dac
EGAC00001002994
-
Ovarian cancer cfDNA dataset DAC
Dac
EGAC00001003234
-
INCLIVA-CC-WES DAC
Dac
EGAC50000000156
-
Metastatic Breast Cancer Data Access Committee
Dac
EGAC00001003074
-
Genomic gain of EBV's LMP-1 in NKTCL
Study
EGAS50000000260
-
The genomic imprint of cancer therapies helps timing the formation of metastases
Study
EGAS00001003416
-
Enhancing OSCC Prediction: The Prognostic Power of WPOI and Tumor Budding, and the Limited Impact of Molecular Resection Margins
Study
EGAS50000000074
-
The tissue origin of highly elevated cell-free DNA in patients with and without cancer
Study
EGAS00001005400
-
Evaluation of Ancestry Admixture among Chileans
Study
phs001385
-
High Density SNP Association Analysis of Melanoma: Case-Control and Outcomes Investigation
Study
phs000187
-
Genome-Wide Association Study of Sporadic and Familial Testicular Germ Cell Tumors
Study
phs001303
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study
Study
phs001101
-
A Multiethnic Genome-wide Scan of Prostate Cancer
Study
phs000306
-
Genomic Sequencing of Pediatric Rhaboid Cancers
Study
phs000508
-
STAMPEED: Whole Genome Association Analysis of Hematopoietic Cell Transplant (HCT) Outcomes
Study
phs001918
-
Gastric Cancer Genetic Analysis of Metastasis
Study
phs000795
-
Study on longer adjuvant chemotherapy in Women with Early Breast Cancer
Study
phs000807
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
Exploiting New Patterns of Genome Damage in Triple Negative Breast Cancer
Study
phs003038
-
Genomic Sequencing of Solitary Fibrous Tumors
Study
phs000568
-
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Study
phs000435
-
Next generation sequencing of diffuse intrinsic pontine glioma samples to identify recurrent mutations, variations, and expression patterns to define novel therapies
Study
phs001526
-
Genome-Wide Predictors of Treatment-Related Toxicities in SWOG S0221 Trial
Study
phs001428
-
Bladder Cancer Organoids as a Functional System to Model Different Disease Stages and Therapy Response
Study
phs003149
-
DNA Methylation Markers and Pancreatic Cancer Risk in 3 Cohort Studies (NHS, PHS, HPFS)
Study
phs001917