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Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
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Molecular evolution and clinical trajectories of prostate cancer identifies novel markers for risk stratification
Study
EGAS00001002923
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Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Study
EGAS00001004235
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Comprehensive cancer predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
Dataset
EGAD00001004088
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ENCORAFENIB COMBINED WITH BINIMETINIB FOR BRAFV600E-MUTATED RELAPSED/REFRACTORY MULTIPLE MYELOMA: THE PHASE II GMMG-BIRMA TRIAL (Hipo_K08K)
Study
EGAS00001005973
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Repli-seq data for 'Replication timing alterations are associated with mutation acquisition during tumour evolution in breast and lung cancer'
Study
EGAS00001007773
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Sequence data for study: Mobilization of tissue-resident memory CD4+ T lymphocytes from bone marrow and their contribution to a systemic secondary immune reaction
Study
EGAS00001005475
-
Single-cell RNA-seq and spatial transcriptomics data for the sarcoidosis baseline project
Study
EGAS00001006970
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MINCR is a MYC-induced lncRNA able to modulate MYC’s transcriptional network in Burkitt lymphoma cells
Dataset
EGAD00001001441
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Exome sequencing of blastic plasmacytoid dendritic cell neoplasms
Dataset
EGAD00001000406
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Preferential infiltration of unique Vγ9Jγ2‐Vδ2 T cells into glioblastoma multiforme
Dataset
EGAD00001004862
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Dataset for colorectal_cancer-RNA
Dataset
EGAD00001008855
-
Dataset for head_and_neck_cancer-RNA
Dataset
EGAD00001008861
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MutWP5: CRUK Mutographs of Cancer: Cancer Mastectomy (Exome)(Novaseq)
Dataset
EGAD00001010117
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Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Dataset
EGAD00001011122
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Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Study
phs000948
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The Atherosclerosis Risk in Communities (ARIC) Study
Study
phs000090
-
PRE-DETERMINE: Biologic Markers and MRI SCD Cohort Study
Study
phs002940
-
Single Cell and Spatial Transcriptomics Studies of Fibrosis in Prospective Registry in IBD Study at MGH and GI Disease and Endoscopy Registry
Study
phs003943
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Comparison of the treated celiac disease microbiome to that of controls
Study
EGAS50000000959
-
RNA-seq of DF149 cells – a patient-derived xenograft model of ascites-derived, homologous recombination repair-proficient, high-grade serous ovarian carcinoma – cultured in vitro and isolated after 8 hours treatment with DMSO control (3 x biological replicates) and 2.5 µM CBL0137 (3 x biological replicates)
Study
EGAS00001006662
-
Whole Genome Study for De Novo Mutation Rates
Study
phs001055
-
Reading about genomic analysis of pan-neuroblastoma
Blog
genomic-analysis-of-pan-neuroblastoma
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Development of a fully human glioblastoma-in-brain-spheroid model for accelerated translational research
Study
EGAS50000000757
-
WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG)
Study
EGAS00001002398
-
The cellular immune and airway epithelial profile throughout childhood and in response to COVID-19 at multi-omic single cell level.
Dataset
EGAD00001007718
-
Dataset for hepatopancreaticobiliary_malignancy-RNA
Dataset
EGAD00001008863
-
Deep whole genome ctDNA chronology of treatment-resistant prostate cancer
Dataset
EGAD00001008460
-
Genomic Advances in Sepsis (GAinS): RNA-seq
Dataset
EGAD00001008730
-
cell-free DNA Whole Genome Sequencing of 3784 samples on MGI and Illumina platform
Dataset
EGAD00001009335
-
Somatic mutation and selection at epidemiological scale - Sanger_NanoSeq_RandD
Dataset
EGAD00001015624
-
Genetics of Human Inherited Retinal Diseases (GHIRD)
Study
phs001517
-
Nanobody-Tethered Transposition Allows for Multifactorial Chromatin Profiling at Single-Cell Resolution
Study
phs003068
-
Whole Genome Sequencing for Metastatic Mutational Burden in Extraskeletal Myxoid Chondrosarcoma
Study
phs003305
-
NHLBI TOPMed: Trans-Omics Analysis for Congestive Heart Failure (TOPCHeF)
Study
phs002038
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
UK10K_COHORT_ALSPAC REL-2011-12-01
Dataset
EGAD00001000195
-
Tumor transcriptome profiling from the OAK and POPLAR randomized clinical trials of atezolizumab in 2L NSCLC
Dataset
EGAD00001007703
-
Dataset for neuroendocrine_adrenal_tumor-RNA
Dataset
EGAD00001008862
-
Targeted and Whole Exome Sequencing for Validation of PGDx elio tissue complete
Dataset
EGAD00001008099
-
RNA-Seq of 584 DLBCL Cases of Non-China Cohort from Phoenix Clinical Trial
Dataset
EGAD00001008131
-
Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea
Study
phs001260
-
The Genomic Landscape of Mongolian Hepatocellular Carcinoma
Study
phs002000
-
GECCO: Detecting Common and Rare Genetic Loci and GxE Interactions in Colorectal Cancer
Study
phs001315
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD) Clinical Trial
Study
phs001411
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
VCRC Imaging Protocol for Magnetic Resonance and Positron Emission Tomography in Large-Vessel Vasculitis (Takayasu's Arteritis): Development as Clinical Trial Outcome Measures Vasculitis Clinical Research Consortium
Study
phs001715
-
Trisomy21: Risk Factors for Chromosome Nondisjunction (T21NDJ)
Study
phs000718
-
The last addition to the list of clonal evolution studies in the EGA
Blog
the-last-addition-to-the-list-of-clonal-evolution-studies-in-the-ega
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NPC genome-wide human SNP array data
Dataset
EGAD00010002296