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Genome and transcriptome sequence data from a neuroendocrine tumor patient
Dataset
EGAD00001011024
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Genome and transcriptome sequence data from a small cell lung carcinoma patient
Dataset
EGAD00001011026
-
Genome and transcriptome sequence data from a nasopharyngeal carcinoma patient
Dataset
EGAD00001011028
-
Genome and transcriptome sequence data from a colorectal carcinoma patient
Dataset
EGAD00001011029
-
Genome and transcriptome sequence data from a pancreatic adenocarcinoma patient
Dataset
EGAD00001011030
-
Genome and transcriptome sequence data from a urachal adenocarcinoma patient
Dataset
EGAD00001011031
-
Genome and transcriptome sequence data from a liposarcoma patient
Dataset
EGAD00001011032
-
Genome and transcriptome sequence data from a gastrointestinal stromal tumor patient
Dataset
EGAD00001011033
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Genome and transcriptome sequence data from a granulosa cell ovarian tumor patient
Dataset
EGAD00001011034
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Genome and transcriptome sequence data from a pancreatic adenocarcinoma patient
Dataset
EGAD00001011035
-
Genome and transcriptome sequence data from a papillary thyroid carcinoma patient
Dataset
EGAD00001011038
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Genome and transcriptome sequence data from a thymoma patient
Dataset
EGAD00001011039
-
Genome and transcriptome sequence data from a rectal adenocarcinoma patient
Dataset
EGAD00001011040
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Whole genome sequencing data of high-grade serous ovarian cancer samples (set 7a)
Dataset
EGAD00001010845
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An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - WGS
Dataset
EGAD00001011645
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
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Combination Immune Checkpoint Inhibition in Australian Rare Cancers_WES
Dataset
EGAD00001015465
-
WGS/WES analysis refines molecular subtypes of hepatocellular carcinoma
Dataset
EGAD00001015428
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Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
Study
JGAS000813
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genes
Study
phs003348
-
Genomic Basis of Phenotypic Variability of Complex Disorders
Study
phs002450
-
A circulating biomarker for severity of facioscapulohumeral muscular dystrophy
Study
EGAS00001007350
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Study
EGAS00001008073
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219
-
The Genomic Landscape of Endocrine Resistant Advanced Breast Cancers: Paired Pre- and Post-endocrine Therapy Samples.
Study
phs001674
-
Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas
Study
phs002380
-
High response rate to anti PD-1 therapy in desmoplastic melanoma
Study
phs001469
-
Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Study
phs000652
-
Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors
Study
phs001906
-
Whole Genome Association Study of Systemic Lupus Erythematosus
Study
phs000122
-
Whole Genome Sequencing for Metastatic Mutational Burden in Extraskeletal Myxoid Chondrosarcoma
Study
phs003305
-
A Therapeutic Vaccine for Fibrolamellar Hepatocellular Carcinoma
Study
phs003970
-
Vaccine-Expanded Plasmablast-like B Cells Are Associated with Response to Dendritic Cell Therapy in Metastatic Melanoma
Study
EGAS50000001177
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
-
Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
-
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
-
Dynamics of checkpoint receptors in γδ T cell subsets are associated with clinical responses during anti-PD-1 immunotherapies
Study
EGAS50000001270
-
Prediction of homologous recombination deficiency identifies colorectal tumors sensitive to PARP inhibition
Study
EGAS50000000426
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
Target gene sequencing for human normal endometrial glands
Study
EGAS00001005914
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
IFN-γ and TNF-α drive a CXCL10+ CCL2+ Macrophage Phenotype Expanded in Severe COVID-19 Lungs and Inflammatory Diseases with Tissue Inflammation
Study
phs002780
-
A Multimodal Atlas of Human Brain Cell Types
Study
phs001791
-
DNA and RNA sequencing of single human haploid germ cells
Study
phs002279
-
Anaplastic oligodendroglioma exome and RNA sequencing data
Study
EGAS00001001209
-
RNA sequencing CYLD cutaneous syndrome
Study
EGAS00001003841
-
Whole genome sequencing data from tumor and normal samples
Dataset
EGAD50000001909
-
13 WGS and 8 TCS data of ENKL patients treated with pembrolizumab.
Dataset
EGAD00001004140
-
Clonal haematopoiesis in patients with AAA (2019-04-03)
Dataset
EGAD00001004895
-
RNAseq of whole blood in 359 idiopathic pulmonary arterial hypertension patients reveals biological heterogeneity
Dataset
EGAD00001007981
-
Functional Significance of Prostate Cancer Risk-SNPs
Study
phs000985
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
Testicular large B-cell lymphoma is genetically similar to PCNSL and distinct from nodal DLBCL
Study
EGAS50000000521
-
Childhood Cancer Data Initiative (CCDI): CCDI Pediatric In Vivo Testing Program - Leukemia
Study
phs003164
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program – Sarcomas and other Solid Tumors
Study
phs003161
-
Application of targeted long-read methylation sequencing to dissected lung cancer tissues
Study
JGAS000757
-
BE_screens_of_WRN_gene_in_MSI_models
Study
EGAS00001006872
-
IMMUcan SCCHN1 cohort
Study
EGAS50000001533
-
Molecular biomarkers in progression from refractory celiac disease to the lethal cancer variety enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001006669
-
Chromosomal instability shapes the tumor microenvironment of oesophageal adenocarcinoma via a cGAS–chemokine–myeloid axis
Study
EGAS50000001561
-
The chemotherapeutic CX-5461 is extremely mutagenic and may increase cancer risk
Study
EGAS50000000023
-
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000813
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000812
-
Ballett
Study
EGAS50000000478
-
Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer
Study
EGAS50000000666
-
Amplicon_based_sequencing_of_drug_resistant_organoids
Study
EGAS00001001639
-
ENU_LS_411N_TripleTherapy
Study
EGAS00001001777
-
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Study
EGAS00001005078
-
Mutational_burden_in_human_hair_follicles
Study
EGAS00001004462
-
Transcriptomic predictors of survival for palbociclib + endocrine therapy vs. capecitabine in aromatase inhibitor-resistant breast cancer from GEICAM/2013-02 PEARL
Study
EGAS00001008177
-
Catalogue Statistics
Documentation
about/statistics/catalogue
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001895
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001894
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001893
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001892
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001891
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by shallow whole genome sequencing
Dataset
EGAD50000001889
-
Exome sequencing of patients with Ewings sarcoma
Dataset
EGAD00001000333
-
Whole genome analyses of the childhood cancer neuroblastoma
Dataset
EGAD00001000282
-
Genome and transcriptome sequence data from a metastatic cholangiocarcinoma patient
Dataset
EGAD00001002976
-
Genome and transcriptome sequence data from a rectal adenocarcinoma patient
Dataset
EGAD00001002973
-
Genome and transcriptome sequence data from a cholangiocarcinoma patient
Dataset
EGAD00001002991
-
Genome and transcriptome sequence data from a leiomyosarcoma patient
Dataset
EGAD00001002996
-
Constit Genome Sequencing
Dataset
EGAD00001003190
-
Whole exome and targeted DNA sequencing data for formalin-fixed paraffin embedded tissue from de novo small cell prostatic carcinoma cases
Dataset
EGAD00001004139
-
SPECTA: NGS Screening Program for Efficient Clinical Trial Access
Dataset
EGAD00001000894
-
Guardians of the genome: protecting DNA from endogenous sources of damage
Dataset
EGAD00001006055
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
Spatial transcriptome sequence data from cross section of cancer containing prostates
Dataset
EGAD00001008644