-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
-
Targeted sequencing of head and neck squamous cell carcinomas
Study
EGAS00001002979
-
Heritable pulmonary arterial hypertension in a large Iberian family
Study
EGAS00001003123
-
65 prostate cancer cases WGS and transcriptome sequencing project
Study
EGAS00001000888
-
Comparison of 3 protocols for deriving pancreatic progenitors from hPSC with RNA-seq and ATAC-seq
Study
EGAS00001003513
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Comprehensive Genomic and Transcriptomic Analysis of Rare Cancers for Guiding of Therapy (H021)
Study
EGAS00001004813
-
Immune trajectory of response and adverse effect in immunotherapy-treated hepatocellular carcinoma
Study
EGAS00001004843
-
Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
-
Longitudinal Single-Cell Profiling Reveals Molecular Heterogeneity and Tumor-Immune Evolution in Refractory Mantle Cell Lymphoma
Study
EGAS00001005019
-
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Study
EGAS00001003828
-
Molecular profiling of metastatic uveal melanoma
Study
EGAS00001004296
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas
Study
EGAS00001004461
-
Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
A microRNA-signature that correlates with cognition and is a target against cognitive decline
Study
EGAS00001005627
-
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD_Full_STDY
Study
EGAS00001003249
-
ENCORAFENIB COMBINED WITH BINIMETINIB FOR BRAFV600E-MUTATED RELAPSED/REFRACTORY MULTIPLE MYELOMA: THE PHASE II GMMG-BIRMA TRIAL (Hipo_K08K)
Study
EGAS00001005973
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Study
EGAS00001005982
-
A Proteogenomic Analysis of Clear Cell Renal Cell Carcinoma in a Chinese Population
Study
EGAS00001006005
-
Oncogenic cooperation in a human de novo T-ALL model
Study
EGAS00001006055
-
Exome sequencing of synchronous colorectal cancers
Study
EGAS00001003474
-
Combined gene expression and digital pathology identifies molecular mediators of T cell exclusion and immune suppression in ovarian cancer
Study
EGAS00001003487
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
Human genome-wide variations in the Massim region
Study
EGAS00001006010
-
Exome & MiSeq sequencing of individuals with Huntington's disease
Study
EGAS00001006383
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Tocilizumab treatment leads to early resolution of myeloid dysfunction and lymphopenia in patients hospitalized with COVID-19
Study
EGAS00001006688
-
Tracking early lung cancer metastatic dissemination in TRACERx using ctDNA
Study
EGAS00001006923
-
Blood transcriptome profiling links immunity to disease severity in myotonic dystrophy type 1 (DM1).
Study
EGAS00001006926
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA
Study
EGAS00001007259
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Genetic Heterogeneity of the familial gastric neuroendocrine tumors (2018-06-06)
Dataset
EGAD00001004153
-
Immune cell atlas of environmental and ancestral diversity in Indonesia [scRNAseq]
Study
EGAS50000001656
-
Immune cell atlas of environmental and ancestral diversity in Indonesia [WGS]
Study
EGAS50000001655
-
Single Cell RNA Transcriptomics of Mantle Cell Lymphoma Reveals the Presence of Treatment-Resistant Subclones at the Time of Diagnosis
Study
EGAS50000000825
-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Study
EGAS00001007327
-
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS)
Study
phs000327
-
The National Institute of Neurological Disorders and Stroke (NINDS) Human Genetics Resource Center: DNA and Cell Line Repository (the NINDS Repository): Motor Neuron/Amyotrophic Lateral Sclerosis (ALS) Study
Study
phs000006
-
Multisite_Breast_Cancer_Whole_Genome
Study
EGAS00001000890
-
Colorectal cancer GWAS on the Spanish population
Dataset
EGAD00010001715
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas for the study and all the datasets.
Dataset
EGAD00010001902
-
Exome Sequencing for brazilian patients with Idiopathic Collapsing Glomerulopathy
Dataset
EGAD50000000091
-
Whole genome bisulfite sequencing of prostate cancer samples upon oral pimonidazole administration
Study
EGAS50000000069
-
Molecular Genetics of Secondary Histiocytic/Dendritic Sarcoma
Study
phs001942
-
Improving Transcriptome Fidelity Following Synovial Tissue Disaggregation
Study
phs002991
-
Investigating differential diagnostic and prognostic biomarkers in primary cutaneous follicle center lymphoma and follicular lymphoma using low-coverage whole-genome sequencing
Dataset
EGAD50000000199
-
Whole-genome sequencing of primary mediastinal large B-cell lymphoma
Study
EGAS50000000340
-
Orthogonal proteogenomic analysis identifies the druggable PA2G4-MYC axis in 3q26 AML
Study
EGAS50000000347
-
Single nuclei RNAseq data from HGSOC primary tumour samples
Study
EGAS50000000249
-
TallFlow - multi-omics
Study
EGAS50000000358
-
Moroccan Genome Project: Sequencing Data from 109 Whole Genomes of Moroccan Individuals
Dataset
EGAD50000000750
-
Early and Late Onset Colorectal Cancer Genomic Data
Dataset
EGAD50000000774
-
Breast cancer risk SNPs converge on estrogen receptor binding sites commonly shared between breast tumors to locally alter estrogen signalling output
Study
EGAS50000000008
-
Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer
Dataset
EGAD50000000941
-
bulk mRNA-seq of iGRAN (CD14neg) cells from CMML patients and healthy donors
Study
EGAS50000000555
-
ATAC-seq, H3K27ac CUT&Tag, and UMI-4C in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Study
EGAS50000000499
-
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
Study
EGAS50000000303
-
HIV-phyloTSI: PANGEA (veSEQ-HIV)
Dataset
EGAD50000001309
-
HIV-phyloTSI: PANGEA (PCR amplicon)
Dataset
EGAD50000001308
-
Human Tumor Atlas Network (HTAN)
Study
phs002371
-
Genomic Characterization of HPV+ Oropharyngeal Tumors
Study
phs003925
-
Comparison between phenotypic-defined stage of blasts and transcriptional profile
Study
EGAS50000000336
-
Whole Exome Sequencing Data of indolent primary renal B-Cell lymphomas
Study
EGAS50000000774
-
WTCCC2 project controls - 1958 British Birth Cohort and National Blood Service
Study
EGAS00000000028
-
Phenotype and genotype correlation analysis in tuberous sclerosis complex
Study
JGAS000688
-
Single-cell RNA-sequencing for peripheral blood mononuclear cells and plasma proteomics data from COVID-19 patients and healthy controls of Japanese
Study
JGAS000783
-
Comprehensive molecular profiling with whole-exome sequencing (WES) and RNA sequencing (RNA-seq) of PDX tumors
Study
JGAS000707
-
Long-read and short-read RNA sequencing of human normal liver organoid with or without SF3B4 overexpression
Study
EGAS50000001131
-
Visium Spatial transcriptomics
Dataset
EGAD50000001506
-
GeoMx digital spatial profiling of NGS mRNA expression in pre-treatment biopsies from patients.
Dac
EGAC50000000774
-
RNA sequencing of skin tissue and peripheral blood mononuclear cells from patients with atopic dermatitis and healthy controls.
Study
JGAS000628
-
Different malignant tumor samples including lung cancer, colon cancer and breast cancer.
Study
JGAS000360
-
Total NF1 sequence in the patients with neurofaibromatosis type1
Study
JGAS000288
-
Multiple myeloma treated with T-cell redirecting immunotherapies
Study
EGAS50000000546
-
Whole-exome sequencing of intrahepatic cholangiocarcinoma tumors with matched normal tissue from the Medical Center – University of Freiburg
Dataset
EGAD50000001926
-
Whole genome sequencing of chondrosarcoma
Study
EGAS00001000505
-
Presence of bacterial infection in brains of patients with Huntington's disease (HD)
Study
EGAS00001003678
-
Clonal_human_oesophagus_punches
Study
EGAS00001007696
-
OCCAMS_Oesophageal_Cancer_Organoids_1
Study
EGAS00001001382
-
Targeted_NanoSeq_Buccal
Study
EGAS00001005925
-
Testing_the_feasibility_of_genome_scale_sequencing_in_routinely_collected_FFPE_cancer_specimens_versus_matched_fresh_frozen_samples
Study
EGAS00001000173
-
GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER
Study
EGAS00001002477
-
Whole_Genome_Sequencing_OMELib__Cord_blood_
Study
EGAS00001007453
-
Human T-bet governs innate and innate-like adaptive IFN-g immunity against mycobacteria.
Study
EGAS00001004504
-
WES used for direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry
Study
EGAS00001002050
-
Whole exome and transcriptome sequencing of biliary tract cancer
Study
EGAS00001000950
-
Chondromyxoid_fibroma
Study
EGAS00001000533
-
Sequencing_melanoma_germlines
Study
EGAS00001002081
-
Single-cell T-cell receptor sequencing of intraepithelial gammadelta T-cells in celiac disease
Study
EGAS00001003897
-
Genomic architecture and evolution of clear cell renal cell carcinomas defined by multiregion sequencing
Study
EGAS00001000667
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001001293
-
Poikiloderma_syndrome_RNAseq
Study
EGAS00001000250
-
Presence of bacterial infection in brains of patients with Parkinson's disease (PD)
Study
EGAS00001003643
-
Effect_of_FAM50_knockout_on_the_transcriptome
Study
EGAS00001004836