-
Dataset for breast_cancer-WHOLE_GENOME
Dataset
EGAD00001008867
-
Dataset for cancer_of_unknown_primary-WHOLE_GENOME
Dataset
EGAD00001008869
-
Dataset for synovial_sarcoma-WHOLE_GENOME
Dataset
EGAD00001008899
-
NLG-LBC-05 ctDNA project sequencing data
Dataset
EGAD00001009337
-
Single Cell Genome Sequence for DLP+ library A110660A
Dataset
EGAD00001009430
-
Single Cell Genome Sequence for DLP+ library A96213A
Dataset
EGAD00001009477
-
Single Cell Genome Sequence for DLP+ library A98181A
Dataset
EGAD00001009479
-
Single Cell Genome Sequence for DLP+ library A95621B
Dataset
EGAD00001009487
-
Breast cancer topographs
Dataset
EGAD00001010124
-
Machine Learning Guided Signal Enrichment for Plasma Tumor-burden Monitoring Dataset
Dataset
EGAD00001011352
-
Timing the Philadelphia chromosome and trajectory to chronic myeloid leukaemia
Dataset
EGAD00001015353
-
Structure and Diversity of Urinary Cell-Free DNA Informative of Host-Pathogen Interactions in Human Urinary Tract Infection
Study
phs001564
-
University of North Carolina at Chapel Hill (UNC) Hepatocellular Carcinoma Study by Exome Sequencing (HCCSES)
Study
phs000627
-
Longitudinal genome-wide analysis of progressive chronic lymphocytic leukemia under uniform front-line therapy of pentostatin, cyclophosphamide, and rituximab
Study
phs000794
-
Adoptive Cell Therapy of Autologous T cell Receptor-Engineered T Cells Targeting the p53 Neoantigens in Human Solid Tumors
Study
phs002928
-
Study of Tumor Recurrence Related to the Expression of the PAX3-FOXO1 Oncogenic Transcription Factor in Fusion-Positive Rhabdomyosarcoma
Study
phs002344
-
Pharmacokinetics and Pharmacogenomics of Ribociclib in Race-Based Cohorts (LEANORA)
Study
phs003770
-
Spatial transcriptomics analysis of triple negative breast cancers
Study
EGAS50000000475
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
-
Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Study
EGAS00001006218
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Distinct genomic profiles and clinical outcomes in constitutional mismatch repair deficiency-associated high-grade gliomas: insights into mutational signatures and clonal evolution
Study
EGAS50000001506
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
Efficacy and safety of entrectinib in patients with ROS1-positive advanced/metastatic non-small cell lung cancer (NSCLC) from the Blood First Assay Screening Trial (BFAST)
Study
EGAS50000000105
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Study
EGAS50000000191
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
Cancer cell and tumor microenvironment biomarkers associated with disease-free survival with adjuvant nivolumab in the phase 3 CheckMate 274 trial
Study
EGAS50000000560
-
IL-27 promotes tumour control by enhancing cytotoxic T cell function
Study
EGAS50000000694
-
The ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge
Study
EGAS00001002092
-
WGS of T-cell and NK-cell lymphoma for ICGC (NKTL-SG)
Study
EGAS00001002398
-
Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Study
EGAS00001005023
-
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD
Study
EGAS00001002896
-
DERMATLAS__Porocarcinoma_RNAseq
Study
EGAS00001005721
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis
Study
EGAS00001004373
-
early-stage ESCC sequencing study
Study
EGAS00001006126
-
Genomic Data of Pediatric MDS
Dataset
EGAD00001007856
-
Whole-genome sequencing of gastric cancer 81 samples in the Japanese population.
Dataset
EGAD00001008610
-
cell-free DNA Whole Genome Sequencing of 3784 samples on MGI and Illumina platform
Dataset
EGAD00001009335
-
Common early-life exposure of the colorectal epithelium to the microbiome-derived mutagen colibactin
Dataset
EGAD00001015830
-
Women's Health Initiative Clinical Trial and Observational Study
Study
phs000200
-
Single-cell bisulfite-seq analyses of 1-year-old prospermatogonia and adult spermatogonial stem cell
Study
JGAS000887
-
Single-cell bisulfite-seq analyses of 29-year-old prospermatogonia and adult spermatogonial stem cell
Study
JGAS000888
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
Validation of SNVs found by Exome-seq in S2-SF1, -SF5 and -SF9 hiPSCs
Dataset
EGAD00001000631
-
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Dataset
EGAD00001011349
-
Pediatric Low-Grade Glioma RNA and Targeted Sequencing
Study
EGAS00001004242
-
Transcriptome human nasal epithelium
Dataset
EGAD00001002226
-
Adult B-precursor acute lymphoblastic leukemia transcriptomes
Dataset
EGAD00001008633
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015379
-
Stand Up 2 Cancer (SU2C) Genomics-Enabled Medicine for Melanoma (GEMM) Trial
Study
phs001786
-
Exploring the evolution of atypical fibroxanthoma to pleomorphic dermal sarcoma: a genomic and pharmacological insight
Study
EGAS50000001741
-
Bulk_sequencing_study_for_human_male_germline
Study
EGAS00001005990
-
Axes of Biological Variation in Diffuse Large B-Cell Lymphoma
Study
EGAS50000001227
-
The_genomic_architecture_of_mesothelioma_
Study
EGAS00001000353
-
PTEN homozygous deletion is a negative prognostic factor in Tumor Treating Fields-treated glioblastoma, IDH wildtype patients
Study
EGAS50000001469
-
Mutational_Signatures_of_relapse_in_rectal_cancer_FFPE_samples_in_the_CR07_clinical_trial
Study
EGAS00001000651
-
Exploration_of__mutational_processes_in_human_cancer_cell_lines__Exome
Study
EGAS00001000790
-
Correlative Genomic Analysis of Durvalumab plus Pazopanib Combination in Patients with Advanced Soft Tissue Sarcomas
Study
EGAS50000000082
-
SOFT_study___sequencing_premenopausal_breast_cancer
Study
EGAS00001000983
-
Colorectal_Adenoma_Gene_Screen
Study
EGAS00001001261
-
FFPE, buffycoat and cell free DNA from N. German esophagus cancer patients - 2021
Study
EGAS00001006813
-
Clonal_selection_after_gene_therapy_in_SCD___Duplex_sequencing
Study
EGAS00001007253
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001898
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001897
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001896
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001890
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001888
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Dataset
EGAD50000001899
-
Whole-exome sequencing (WES) analysis of untreated head and neck cancer patient-derived xenografts (PDXs) matched patient tumor tissue and normal mucosa tissue.
Dataset
EGAD50000002325
-
Cergentis FFPE-TLC sequencing of colorectal carcinoma
Dataset
EGAD50000000618
-
Genomic Rearrangements in Pediatric Cancer
Dataset
EGAD00001007701
-
Monotherapy Breast Cancer
Dataset
EGAD00001000349
-
Somatic pseudogenes acquired during cancer development – Whole Exome sequencing
Dataset
EGAD00001000637
-
Somatic pseudogenes acquired during cancer development – Whole Genome sequencing
Dataset
EGAD00001000638
-
Somatic pseudogenes acquired during cancer development – RNAseq
Dataset
EGAD00001000639
-
RNAseq of patients with Ewings sarcoma
Dataset
EGAD00001000444
-
Matched Pair Cell Line Tumour RNAseq
Dataset
EGAD00001000630
-
FFPE CPA Accreditation Study Part 2
Dataset
EGAD00001000868
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)
Dataset
EGAD00001005017
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGBS)
Dataset
EGAD00001005018
-
Deep targeted DNA sequencing dataset for the study "Molecular characteristics in Burkitt lymphoma over age groups"
Dataset
EGAD00001007708
-
WGS and Avenio Surveillance Panel data to previously submitted data under study number EGAS00001004276 of ALK-rearranged lung cancer
Dataset
EGAD00001007818
-
Dataset for Ewing_sarcoma_PNET-WHOLE_GENOME
Dataset
EGAD00001008874
-
Dataset for colorectal_cancer-WHOLE_GENOME
Dataset
EGAD00001008872
-
Dataset for Ewing_sarcoma_PNET-EXON
Dataset
EGAD00001008873
-
Dataset for gynecologic_cancer-EXON
Dataset
EGAD00001008877
-
Dataset for liposarcoma-EXON
Dataset
EGAD00001008886
-
Dataset for melanoma-WHOLE_GENOME
Dataset
EGAD00001008889
-
Dataset for NSCLC-EXON
Dataset
EGAD00001008892
-
Dataset for synovial_sarcoma-EXON
Dataset
EGAD00001008898
-
WGS of cell-free DNA derived from plasma of CRC patients and healthy controls, and WGS of matched tumor tissue and saliva
Dataset
EGAD00001009309
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 3)
Dataset
EGAD00001009888
-
Genome and transcriptome sequence data from a melanoma patient
Dataset
EGAD00001011022
-
Genome and transcriptome sequence data from a follicular lymphoma patient
Dataset
EGAD00001011023