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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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Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001004192
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Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Study
EGAS00001007108
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Osteosarcoma_Whole_Genome
Study
EGAS00001000147
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DPY30_ChIP_seq
Study
EGAS00001001132
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Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
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Whole_Genome_sequencing_of_individuals_from_Carlantino__Italy
Study
EGAS00001000460
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Egypt_Genome_Project___low_coverage_whole_genome_sequencing
Study
EGAS00001000480
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ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
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CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
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Analysis of DNA methylation in normal B cells and chronic lymphocytic leukemia
Study
EGAS00001000534
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Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
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Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
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A sequence-based genetic dissection of human immune cell types and implications for immune-related disease.
Study
EGAS00001000574
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Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
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Genome-wide SNP genotyping of Central African rainforest hunter-gatherers and neighbouring agriculturalists
Study
EGAS00001000605
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JMML targeted sequencing (2013)
Study
EGAS00001001324
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The molecular landscape of colorectal cancer (17 cases)
Study
EGAS00001002174
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Osteosarcoma_RNAseq
Study
EGAS00001000615
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BLUEPRINT ChIP-seq data for cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000326
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Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
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H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
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Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
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Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
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Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
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MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
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Identification_of_rare_variants_associated_with_cardiovascular_traits_in_Cilento_isolates
Study
EGAS00001000620
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Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
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Breast_Cancer_Matched_Pair_Cell_Line_Whole_Genomes
Study
EGAS00001000166
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Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
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Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
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Combination_therapies_for_personalized_cancer_medicine
Study
EGAS00001000655
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BASIS_RNAseq
Study
EGAS00001000707
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Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
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Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
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PAGE: Prenatal Assessment of Genomes and Exomes
Study
EGAS00001001713
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Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
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Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
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Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
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Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
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Assessment_of_epigenetic_variation_in_human_iPS_cells_Medip
Study
EGAS00001000741
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Pangenomic classification of pituitary adenomas
Study
EGAS00001003642
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Ashkenazi Jewish Leukoencephalopathy
Study
EGAS00001001767
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Whole genome sequencing of six ethnic groups from Burkina Faso, Cameroon, and Tanzania
Study
EGAS00001003648
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Systems biology of Colorectal Cancer
Study
EGAS00001000854
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UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
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Succession Of Transiently Active Tumour-Initiating Cell Clones inHuman Pancreatic Cancer
Study
EGAS00001000882
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Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Study
EGAS00001003736