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Error-corrected flow-based sequencing at whole genome scale and its application to circulating cell-free DNA profiling
Study
EGAS50000000844
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Whole exome sequencing of bladder tumors
Study
EGAS50000001248
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MATISSE WES and bulk RNA-sequencing data
Study
EGAS50000001003
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Single-cell multidimensional profiling of tumor cell heterogeneity in supratentorial ependymomas
Study
EGAS50000001513
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Non-small cell lung cancer molecular subtypes and vulnerability to immunotherapy treatment combinations
Study
EGAS50000001272
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Dynamics of checkpoint receptors in γδ T cell subsets are associated with clinical responses during anti-PD-1 immunotherapies
Study
EGAS50000001270
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FLT3-targeting and places FLT3 as an ideal therapeutic target to selectively eradicate LSCs, while sparing HSC.
Study
EGAS50000000437
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Proteomic predictors of individualized nutrient-specific insulin secretion in health and disease
Study
EGAS00001007241
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Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis, modulating disease
Study
EGAS50000000894
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A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Study
EGAS50000001203
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Whole-genome methylation profiling of menstrual stem cells identifies novel biomarkers for endometriosis
Study
EGAS50000001640
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Non-canonical NF-κB signaling skews B cells away from germinal center to low-affinity effector fate
Study
EGAS50000001646
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Submitters and requesters Statistics
Documentation
about/statistics/community
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Adaptive Therapy Exploits Fitness Deficits in Chemotherapy-Resistant Ovarian Cancer to Achieve Long-Term Tumor Control Open Access
Study
EGAS50000001142
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Whole Genome Sequencing of Neuroblastoma
Study
EGAS00001000222
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Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
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Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
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Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
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Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma
Study
EGAS00001001953
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WTCCC2 Visceral Leishmaniasis (VL) samples
Study
EGAS00001000773
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Global Anaplastic Thyroid Cancer Initiative
Study
EGAS00001002234
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Field_effect_of_healthy_and_diseased_livers_WGS
Study
EGAS00001002413
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Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
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Duplexseq_of_the_interstrand_crosslinks_WGS
Study
EGAS00001006545
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SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons
Study
EGAS00001003436
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Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
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Spatial multi-omic map of human myocardial infarction
Study
EGAS00001006330
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scRNA-seq of HSPC treated with gemcitabine and carbplatin
Study
EGAS00001004381
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Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007602
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Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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SINGLE-CELL RNA SEQUENCING Single-cell RNA sequencing was performed on 13 ‘mild-moderate’ and 10 ‘critical’ COVID19 PBMC samples
Study
EGAS00001005039
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SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
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Transcriptomes of human CD4+ T lymphocytes - Metabolic project
Study
EGAS00001005565
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Single-nucleus transcriptomic profiling of aging Down Syndrome brains
Study
EGAS00001005691
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Increased mutation accumulation during fetal development in Down syndrome
Study
EGAS00001003982
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The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
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Cross-tissue transcriptomic analysis of human secondary lymphoid organ residing ILC3 reveals a default quiescent state in the absence of inflammation
Study
EGAS00001002636
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The identification of genetic vulnerabilities in head and neck cancers for the development of novel treatments.
Study
EGAS00001002682
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Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
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An alternative splicing modulator decreases mutant HTT and improves the molecular fingerprint in Huntington’s disease patient neurons
Study
EGAS00001006289
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Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
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UK10K_OBESITY_GS
Study
EGAS00001000242
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The mission of the BIOS Consortium is to create a large-scale data infrastructure and to bring together BBMRI researchers focusing on integrative omics studies in Dutch Biobanks.
Study
EGAS00001001077
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Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
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Genome-wide cell-free DNA fragmentation in patients with cancer
Study
EGAS00001003611
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Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
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Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
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Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736
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RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
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Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
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Oncoprint GSCCs
Study
EGAS00001007481
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Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
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Widespread DNA hypomethylation and differential gene expression in Turner syndrome
Study
EGAS00001002190
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Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
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We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670
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Gut microbiome modulates response to anti PD1 immunotherapy in metastatic melanoma patients
Study
EGAS00001002698
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Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
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SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS
Study
EGAS00001000764
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H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
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Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
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Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
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Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
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Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
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Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007604
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noninvasive lung cancer subtyping
Study
EGAS00001007717
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An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
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The Ovarian Cancer Association Consortium OncoArray genome-wide association study
Study
EGAS00001002305
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Whole Mitochondrial Sequencing of Gingivo-buccal Cancer: ICGC-India Project
Study
EGAS00001002425
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The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
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Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Study
EGAS00001002737
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Defective T-cell expansion in RASGRP1 deficiency
Study
EGAS00001002753
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Somatic IL4R Hotspot Mutations in Primary Mediastinal Large B-cell lymphoma lead to constitutive JAK-STAT activation
Study
EGAS00001002796
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Hominin-specific NOTCH2 paralogs expand human cortical neurogenesis through regulation of Delta/Notch interactions.
Study
EGAS00001002798
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PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Study
EGAS00001002903
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Japan PBC-GWAS Haplotype Study
Study
EGAS00001002915
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Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
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Ewings Sarcoma RNA-Seq
Study
EGAS00001003062
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Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
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Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis -Part II
Study
EGAS00001003357
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Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
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Integrative_genome_profiling_in_AML
Study
EGAS00001000858
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HCA_Thymus_Disease
Study
EGAS00001004310
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Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
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Clinical significance of novel subtypes of acute lymphoblastic leukemia in the context of minimal residual disease-directed therapy
Study
EGAS00001005084
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An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_
Study
EGAS00001000134
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Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (microarray)
Study
EGAS00001004755
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UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
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BIOKEY: A single-cell catalogue of the dynamic changes underlying Checkpoint Immunotherapy response in Early Breast Cancer
Study
EGAS00001004809
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Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Study
EGAS00001003286
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Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
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The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
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Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
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Identification of rare germline variants in familial multiple myeloma
Study
EGAS00001004734
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Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
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ARAF Mutations Confer Resistance to RAF Dimer Inhibitor Belvarafenib in NRAS- and BRAF- Mutant Melanoma
Study
EGAS00001005086
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Risk and modifying factors in Frontotemporal Dementia
Study
EGAS00001004895
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Comparative transcriptome of CD34+ hematopoietic progenitors from myeloproliferative patients and control donors
Study
EGAS00001005106
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Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Study
EGAS00001005144
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Epigenome wide DNA methylation assay of gingivo-buccal oral squamous cell carcinoma using single base resolution high throughput array
Study
EGAS00001003896
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Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Study
EGAS00001005196