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Germline WES of serrated polyposis syndrome
Study
EGAS50000000765
-
ACUITI
Study
EGAS50000000962
-
IDH- and H3-wildtype high-grade gliomas in teenagers and young adults
Study
EGAS50000000641
-
WES - Characterization of a Breast Patient-derived Tumor Organoid biobank from an underserved population of patients.
Study
EGAS50000000684
-
Sensitive neoantigen discovery by real-time mutanome-guided immunopeptidomics - WES
Study
EGAS50000000976
-
Whole Exome Sequencing of Human Gastro-esophageal Cancer PDXs
Study
EGAS50000000966
-
Whole-exome variant calling of individuals from the study of sepsis and acute distress respiratory syndrome in Spain
Study
EGAS50000001119
-
Expanding the SPTBN1 Spectrum: A Case of Neurodevelopmental Disorder with GI and Musculoskeletal Involvement
Study
EGAS50000001213
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Acute lymphoblastic leukemia in children produces endogenous T-cells targeting tumor associated antigens and neoantigens in peripheral blood
Study
EGAS50000000925
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PEVOsq
Study
EGAS50000000731
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
Whole Exome Sequencing of Waldenström Macroglobulinemia (WM) Precursor Conditions
Study
EGAS50000001249
-
Response to tumor-infiltrating lymphocyte adoptive therapy is associated with preexisting CD8+ T-myeloid cell networks in melanoma
Study
EGAS50000001217
-
WES-based association study of cefaclor-induced anaphylaxis
Study
EGAS50000001163
-
Excised DNA Circles from V(D)J Recombination Promote Relapsed Leukaemia
Study
EGAS50000001043
-
Exome Sequencing of familial and sporadic Meniere disease patients
Study
EGAS50000001178
-
Exome sequencing for identifying point mutations driving M haemophilum susceptibility
Study
EGAS50000001076
-
Disease recurrence after pathologic response (Recurrence DNAseq)
Study
EGAS50000000488
-
TRACERx NSCLC - Whole exome multiregion sequencing data
Study
EGAS00001006494
-
Integrated drug screening and molecular profiling in pediatric AML
Study
EGAS50000001083
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (Owen)
Study
EGAS00001005855
-
Lessons learned from the exome sequencing of nine cases of infertility and the way forward
Study
EGAS50000001320
-
Germline WES-data of pediatric cancer patients with variants in HBOC-related genes
Study
EGAS50000001073
-
ICARUS-BREAST01-ExomeSeq
Study
EGAS50000000542
-
Whole-exome variant calling of individuals from the study of familial pulmonary fibrosis in the Canary Islands
Study
EGAS50000000782
-
NOUS-209 off-the-shelf immunotherapy has the potential to hit primary and metachronous colorectal and urothelial cancer in Lynch syndrome
Study
EGAS50000001336
-
Genetic differences between primary colorectal cancer and its paired synchronous and metachronous metastases
Study
EGAS50000000996
-
Identification of putative multiple myeloma (MM) susceptibility genes
Study
EGAS50000001259
-
Whole exome sequencing of bladder tumors
Study
EGAS50000001248
-
WES analysis of paired tumor and non-tumoral DNA of 4 patients with non-muscle-invasive bladder cancer
Study
EGAS50000001382
-
Prevalence and association of microsatellite instability and Lynch syndrome Pan-Cancer and development of a personalized cancer risk prediction tool for Lynch syndrome carriers in India
Study
EGAS50000001449
-
Molecular profiles in early onset prostate cancer
Study
EGAS50000001467
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
WES sequencing of metastatic colorectal cancer patient-derived xenografts with known response to irinotecan.
Study
EGAS50000001484
-
Neoadjuvant immune checkpoint blockade in mismatch-repair proficient colon cancers
Study
EGAS50000000856
-
NAR-GAB 2025 deposit data
Study
EGAS50000001456
-
Identification of New Therapeutic Targets for Renal Medullary Carcinoma via Integrated Genomic and Transcriptomic Profiling
Study
EGAS50000001280
-
Variability in immune response genes and prediction of severe SARS-CoV-2 infection (INMUNGEN-Cov2 project)
Study
EGAS50000000066
-
Genomic Data from Patients with Advanced Rare Cancers Treated with Pembrolizumab
Study
EGAS50000001508
-
Germline Aberrations of PAX5 Cause Susceptibility to pre-B cell Acute Lymphoblastic Leukemia
Study
EGAS00001000447
-
ERDERA Diagnostic Research Workstream - WES reanalysis (distributed approach)
Study
EGAS50000001514
-
Whole Exome Sequencing of monomorphic epitheliotropic intestinal T-cell lymphoma and enteropathy associated T-cell lymphoma
Study
EGAS50000001126
-
A human induced pluripotent stem cell toolbox for studying sex chromosome effects-Whole exome seq
Study
EGAS50000000930
-
Proteomic Characterization of Intrahepatic Cholangiocarcinoma Identifies Risk-Stratifying Subgroups, Proteins Associated with Time-To-Recurrence, and mTOR Effector Molecule EIF4A1 as a Druggable Therapeutic Target
Study
EGAS50000001343
-
WES of Mino-VEN-R Mantle Cell Lymphoma Cells
Study
EGAS50000001088
-
Using Exome-sequencing to characterize the resistance to lirafugratinib
Study
EGAS50000001371
-
Rare germline variants in patients with personal and family history of colorectal cancer
Study
EGAS50000000606
-
Heritable pulmonary arterial hypertension - new genetic findings and environmental triggers
Study
EGAS50000001275
-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
Common origin and somatic mutation patterns of composite lymphomas and leukemias
Study
EGAS50000001017