-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
Immune landscape of oncohistone-mutant gliomas reveals diverse myeloid populations and tumor-promoting behavior
Study
EGAS00001007510
-
A clinically applicable connectivity signature for glioblastoma includes the tumor network driver CHI3L1
Study
EGAS00001007611
-
The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma
Dataset
EGAD00001007033
-
The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma
Dataset
EGAD00001007034
-
Transcriptional profiling of tauopathies in human IPS-derived neurons (2019-08-21)
Dataset
EGAD00001005277
-
Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Study
EGAS00001005753
-
ARHGAP11A Maintains Cortical Progenitor Identity Through RHOA–ROCK Signalling During Human Brain Development
Study
EGAS00001008322
-
Single Cell RNA Transcriptomics of Mantle Cell Lymphoma Reveals the Presence of Treatment-Resistant Subclones at the Time of Diagnosis
Study
EGAS50000000825
-
MALT1 in MCL data access commitee
Dac
EGAC00001002989
-
Participating PI's in the Asia Diversity Project
Dac
EGAC00001000565
-
Epigenetic dysregulation in autism spectrum disorder
Dac
EGAC00001000547
-
Whole exome sequencing in cardiovascular patients
Dac
EGAC00001000621
-
Plasma pQTLs in INTERVAL cohort
Dac
EGAC00001000695
-
BCR Signaling in human BM PC
Dac
EGAC00001001899
-
EPICC: Evolutionary Predictions in Colorectal Cancer
Dac
EGAC00001002299
-
EPICC: Evolutionary Predictions in Colorectal Cancer
Dac
EGAC00001002592
-
Mutagenesis in Medicine Data Access Committee
Dac
EGAC50000000026
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: SWISS-AF/SWISS-AF-PVI/BEAT-AF
Study
phs002242
-
CIDR: NINDS High Throughput Genotyping Resource Access for Structural Hindbrain Disorders
Study
phs002621
-
Multisite_Breast_Cancer_Whole_Genome
Study
EGAS00001000890
-
Set_of_human_mesenchymal_CSA
Dataset
EGAD00010002515
-
Investigating differential diagnostic and prognostic biomarkers in primary cutaneous follicle center lymphoma and follicular lymphoma using low-coverage whole-genome sequencing
Dataset
EGAD50000000199
-
BipEx-Landen: Bipolar Exome Sequencing
Dataset
EGAD50000000307
-
TallFlow - multi-omics
Study
EGAS50000000358
-
Breast cancer risk SNPs converge on estrogen receptor binding sites commonly shared between breast tumors to locally alter estrogen signalling output
Study
EGAS50000000008
-
bulk mRNA-seq of iGRAN (CD14neg) cells from CMML patients and healthy donors
Study
EGAS50000000555
-
SALTO: chromosomal copy number alterations to predict response to bevacizumab
Study
EGAS50000000711
-
Dataset for "HPV integration induces gene fusions" (RNA)
Dataset
EGAD50000001303
-
Spatial and temporal transcriptome analysis on human skeletal muscle regeneration
Dataset
EGAD50000000263
-
Dataset for single cell transcriptome sequencing
Dataset
EGAD50000001549
-
SCANDARE HNSCC
Study
EGAS50000001158
-
Amplicon sequencing of duodenal adenoma
Study
JGAS000352
-
Variant calling dataset from the whole-exome study of sepsis and acute distress respiratory syndrome in Spain
Dataset
EGAD50000001613
-
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Study
phs001672
-
GeoMx digital spatial profiling of NGS mRNA expression in pre-treatment biopsies from patients.
Dac
EGAC50000000774
-
singel cell RNAseq dataset for the study "Longitudinal Multi-Omics Study Reveals Molecular Drivers and Tumor Microenvironment in Extramedullary Multiple Myeloma"
Dataset
EGAD50000000053
-
Whole Genome Sequencing Analysis of Adult T-cell Leukemia/Lymphoma
Study
JGAS000320
-
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
-
Resolution and methylation patterns of supernumerary marker chromosomes
Study
EGAS50000001466
-
Exome data from 154 patients with childhood or adolescent cutaneous melanoma
Dataset
EGAD50000001868
-
MissionBio single cell DNA and protein seq for 2 samples
Dataset
EGAD50000001793
-
Clonal_human_oesophagus_punches
Study
EGAS00001007696
-
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
-
Chondromyxoid_fibroma
Study
EGAS00001000533
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001001293
-
Genome-wide characterization of Arabian Peninsula populations
Study
EGAS00001003335
-
H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers
Study
EGAS00001006645
-
Chronic lymphocytic leukemia patient-derived xenografts recapitulate clonal evolution to Richter transformation
Study
EGAS00001006965
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Dataset
EGAD00001006287
-
Second primary vs. primary bowel malignancies
Dataset
EGAD00001008476
-
Short-read (RNA-seq)
Dataset
EGAD00001006596
-
Tumor evolutionary trajectories during the acquisition of invasiveness in early stage lung adenocarcinoma
Dataset
EGAD00001006457
-
Moles (2019-04-01)
Dataset
EGAD00001004876
-
S:CORT Stratification in COloRecTal cancer
Dataset
EGAD00001009760
-
Low-coverage whole-genome sequencing (lcWGS) data of Genome in a Bottle (GIAB) reference samples
Dataset
EGAD00001015533
-
WES on tumor DNA and germline DNA in pediatric cancer
Dataset
EGAD00001007816
-
Germline variants in childhood melanoma
Dataset
EGAD00001010039
-
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Dataset
EGAD00001008317
-
Exome sequencing in a consanguineous family with hypoaldosteronism identtifying LGR4 mutations
Dataset
EGAD00001009761
-
Whole genome sequencing data to study therapeutic targeting of ependymoma
Dataset
EGAD00001003940
-
Resistance to MAPK-inhibitor induces internal duplication in BRAF_Oscar Krijsman
Dataset
EGAD00001001846
-
SEQCAP_Internation_1q_Type_2_Consortium - Agilent SureSelec
Dataset
EGAD00001000421
-
EGA dataset for High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube
Dataset
EGAD00001003792
-
Abnormal foetal development exome trios
Dataset
EGAD00001001442
-
Exome sequencing of serially transplanted genetically marked IC-enriched primary PDAC cultures.
Dataset
EGAD00001000884
-
Triple Negative Breast Cancer Whole Genome Validations
Dataset
EGAD00001000662
-
Oliocapture sequencing libraries from the study "Histological Transformation and Progression in Follicular Lymphoma: a Clonal Evolution Study".
Dataset
EGAD00001002898
-
340 human whole genome sequences from Angola and Mozambique
Dataset
EGAD00001011992
-
Single cell characterization of arrested B-lymphoid differentiation and leukemic cell states in ETV6-RUNX1-positive pediatric leukemia
Dataset
EGAD00001006074
-
Long-read data (PacBio)
Dataset
EGAD00001006597
-
Studies in the Natural History and Pathogenesis of Childhood-Onset and Adult-Onset Idiopathic Inflammatory Myopathies
Study
phs003270
-
Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)
Study
phs000361
-
Experimental PfSPZ Vaccine in Adults Without Malaria
Study
phs002422
-
Whole Genome Sequencing in the Inner City Asthma Consortium (ICAC) Cohorts
Study
phs002921
-
Resistance Development in Basal Cell Nevus Syndrome through the Basal to Squamous Transition
Study
phs003415
-
CONNECTS Master Protocol for Clinical Trials targeting Macro- and Micro-Immuno-Thrombosis, Vascular Hyperinflammation, and Hypercoagulability and Renin-Angiotensin-Aldosterone System (RAAS) in Hospitalized Patients with COVID-19 (ACTIV-4 Host Tissue)
Study
phs003708
-
Yale SPORE in Skin Cancer Project 2
Study
phs002289
-
Genetic Studies of Homologous Recombination Deficiency in Hispanic Gastric Cancer
Study
phs003251
-
CSER: Evaluating Utility and Improving Implementation of Genomic Sequencing for Pediatric Cancer Patients in the Diverse Population and Healthcare Settings of Texas: The KidsCanSeq Study
Study
phs002378
-
Response to tumor-infiltrating lymphocyte adoptive therapy is associated with preexisting CD8+ T-myeloid cell networks in melanoma
Study
EGAS50000001217
-
High-coverage whole-genome sequencing reveals structural variations in triple-negative breast cancer
Study
JGAS000095
-
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
-
Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Study
EGAS00001002737
-
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
-
FASTQ files of total RNA-Seq data of POPS control samples
Dataset
EGAD00001003457
-
Best Endovascular vs. Best Surgical Therapy in Patients With Critical Limb Ischemia (BEST CLI-BioLINCC)
Study
phs003844
-
National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500)
Study
phs000958
-
Transcriptome of CD4+ T cells and CD8+ T cells in glioblastoma multiforme
Dataset
EGAD50000000226
-
High Density SNP Association Analysis of Lung Cancer
Study
phs000753
-
NIMH Human Middle Temporal Gyrus (MTG) Cell Types
Study
phs001790
-
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Study
phs000827
-
Drug screening of patient-derived organoids from colorectal peritoneal metastases
Study
phs002023
-
Ischemic Stroke Genetics Study (ISGS)
Study
phs000102
-
Natural History, Pathogenesis and Outcome of Melorheostosis
Study
phs001976
-
Osteosarcoma Genomics
Study
phs000699
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
Single-cell RNA-seq of rheumatoid arthritis synovial tissue using low-cost microfluidic instrumentation
Study
phs001529