-
Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Dataset
EGAD00001000974
-
hereditary BrEAst Case CONtrol study (BEACCON)
Dataset
EGAD00001007025
-
WGS dataset for Genomic rearrangements in Pediatric Cancer
Dataset
EGAD00001008272
-
sWGS of core biopsies from localized breast cancer patients
Dataset
EGAD00001008397
-
Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing
Dataset
EGAD00001006088
-
META-PRISM
Dataset
EGAD00001009684
-
CNS Embryonal tumors
Dataset
EGAD50000000298
-
National Cancer Institute - Population Structure and Natural Selection in the Epidemiology of Burkitt Lymphoma in East African Children and Minors (EMBLEM) study in Uganda
Study
phs001705
-
Identification of RNA biomarkers in Parkinson's disease patients
Study
JGAS000119
-
LCLF1.0 Data
Study
phs003187
-
CAGE-seq analysis of osteoblast derived from cleidocranial dysplasia human induced pluripotent stem cells
Study
JGAS000248
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
APOBEC mutagenesis is a common process in normal human small intestine
Dataset
EGAD00001008764
-
Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
Study
JGAS000052
-
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Study
phs001222
-
Phase 1 CX-5461 Trial (Canadian Cancer Trials Group Trial IND.231)
Study
EGAS00001006173
-
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Study
EGAS00001003892
-
Molecular subsets in renal cancer determine outcome to checkpoint and angiogenesis blockade
Study
EGAS00001004353
-
The evolution of hematopoietic cells under cancer therapy
Study
EGAS00001005234
-
UK renal cancer samples genotyped on Illumina OmniExpress BeadChip
Study
EGAS00001002336
-
Accumulation of copy number alterations and clinical progression across advanced prostate cancer
Study
EGAS00001006251
-
Constitutional and somatic genomic rearrangements coherently restructure chromosome 21 in acute lymphoblastic leukaemia
Dataset
EGAD00001000658
-
Natural history of clonal haematopoiesis (2017-09-04)
Dataset
EGAD00001003703
-
Molecular diagnosis of albinism (2018-03-14)
Dataset
EGAD00001004039
-
Spiradenocarcinoma (2018-10-29)
Dataset
EGAD00001004426
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Dataset
EGAD00001005938
-
ANGIOPREDICT - an FP7-funded project enabling personalised medicine for patients with metastatic colorectal cancer.
Dataset
EGAD00001008463
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
Genetic Determinants of EGFR-Driven Lung Cancer Growth and Therapeutic Response In Vivo
Study
phs002334
-
Spatial Transcriptomics Reveals Discrete Tumor Microenvironments and Autocrine Loops Within Ovarian Cancer Subclones
Study
phs003561
-
Identification and targeting of extremely high-risk gamma delta T-ALL in children
Study
EGAS50000000018
-
The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer
Study
EGAS00001005984
-
Genomic determinants of response and resistance to inotuzumab in B-ALL
Study
EGAS50000000067
-
Oncogenic FOXL2C134W has gain-of-function chromatin remodeling activity that reprograms glucocorticoid receptor occupancy to promote ovarian granulosa cell tumor growth
Study
EGAS50000000622
-
Comprehensive genomic and transcriptomic analysis of three synchronous primary tumours and a recurrence from a head and neck cancer patient
Study
EGAS00001004857
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. WES
Study
EGAS50000000568
-
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Study
EGAS00001005108
-
Pyjacker identifies enhancer hijacking events in acute myeloid leukemia including MNX1 activation via deletion 7q
Study
EGAS50000000743
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
CSER: South-Seq: DNA Sequencing for Newborn Nurseries in the South
Study
phs002307
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
Discrepancies in Tumour Mutation Burden (TMB) reporting from sequential Endobronchial ultrasound trans bronchial needle aspiration (EBUS TBNA) samples within single lymph node stations
Study
EGAS00001007484
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Clinical outcomes in ctDNA-positive urothelial carcinoma patients treated with adjuvant immunotherapy
Study
EGAS00001004997
-
Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Dataset
EGAD00001009076
-
Mechanisms_of_patient_response_to_Dabrafenib_in_Melanoma
Study
EGAS00001000946
-
Tumor transcriptome profiling from the OAK and POPLAR randomized clinical trials of atezolizumab in 2L NSCLC
Dataset
EGAD00001007703
-
Single-cell profiling of neoantigen-specific T cells in lung cancers treated with neoadjuvant PD-1 blockade
Dataset
EGAD00001007728
-
Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Dataset
EGAD00001007858