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Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
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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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WTCCC2 Visceral Leishmaniasis (VL) samples
Study
EGAS00001000773
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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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UK10K_OBESITY_GS
Study
EGAS00001000242
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Genomic analysis of Smoothened inhibitor resistance in basal cell carcinoma
Study
EGAS00001000845
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Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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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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RNA sequencing and Illumina 2.5M SNP array data collected from 675 commonly used human cancer cell lines.
Study
EGAS00001000610
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Determination_of_cell_specific_regulatory_enhancers_in_hematopoetic_models
Study
EGAS00001000586
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Comprehensive molecular profiling identifies novel genetic drivers and subtypes underlying medulloblastoma
Study
EGAS00001001953
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SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS
Study
EGAS00001000764
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Widespread DNA hypomethylation and differential gene expression in Turner syndrome
Study
EGAS00001002190
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Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
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Whole genome and transcriptome analysis of medullary thyroid cancer
Study
EGAS00001001473
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Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
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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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An_exome_sequencing_study_of_the_HIV_elite_long_term_non_progressors_and_rapid_progressors__CASCADE_cohorts_
Study
EGAS00001000522
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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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Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
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Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
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An_evaluation_of_different_strategies_for_large_scale_pooled_sequencing_study_design_
Study
EGAS00001000134
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Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
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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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De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
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Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
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Whole genome sequencing of retinoblastoma reveals the diversity of rearrangements disrupting RB1 and uncovers a treatment related mutational signature
Dataset
EGAD00001006431
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Targeted and Whole Exome Sequencing for Validation of PGDx elio tissue complete
Dataset
EGAD00001008099
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FASTQ files of total RNA-Seq data of POPS control samples
Dataset
EGAD00001003457
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MutWP1: CRUK Grand Challenge Mutographs of Cancer: Oesophageal adenocarcinoma
Dataset
EGAD00001006083
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Changes in alternative splicing and associated neo-antigens due to therapy
Study
EGAS00001004524
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Transgenerational transmission of reproductive and metabolic dysfunction in the male progeny of polycystic ovary syndrome
Study
EGAS00001007079
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Global Anaplastic Thyroid Cancer Initiative
Study
EGAS00001002234
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Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
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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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Oncoprint GSCCs
Study
EGAS00001007481
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Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
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Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736
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Spatial multi-omic map of human myocardial infarction
Study
EGAS00001006330
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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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Duplexseq_of_the_interstrand_crosslinks_WGS
Study
EGAS00001006545
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MECOM represses myeloid differentiation through CEBPA downregulation in AML
Study
EGAS00001008005
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Genomic_Advances_in_Sepsis__GAinS__genotyping
Study
EGAS00001007786
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Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
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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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Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia
Study
EGAS00001006947
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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