-
Genomics of pediatric myeloid neoplasms
Study
EGAS00001005760
-
ALPI deficiency and inflammatory bowel disease
Study
EGAS00001002847
-
iNeuron_ChIPseq
Study
EGAS00001003165
-
Circulating tumour DNA abundance and potential utility in de novo metastatic prostate cancer
Study
EGAS00001003351
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Analysis of copy number variation landscape of glioma by shallow coverage whole genome sequencing
Study
EGAS00001003690
-
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Study
EGAS00001002333
-
Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER)
Study
EGAS00001004157
-
Degradation of Janus kinases in CRLF2-rearranged acute lymphoblastic leukemia
Study
EGAS00001005180
-
Pediatric tumor in a single child of three large nuclear families
Study
EGAS00001005321
-
Risk alleles of membranous nephropathy and recurrence of the disease on the grafted kidney
Study
EGAS00001005435
-
Identification of fusion transcripts by RNA-sequencing and Whole genome sequencing of a METABRIC patient sample
Study
EGAS00001002475
-
Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors
Study
EGAS00001002645
-
Targeted exome sequencing of pleomorphic invasive lobular carcinoma (PILC).
Study
EGAS00001002871
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Targeted sequencing of breast cancers with germline BRCA1/2 mutations
Study
EGAS00001004182
-
Single cell RNA-sequencing (scRNA-seq) of the human hematopoietic stem cell compartment (CD34+CD38-CD45RA-)
Study
EGAS00001004769
-
RNASeq of PDX and CDX tumours treated with ADC
Study
EGAS00001004562
-
HYPERMUTATION AND MALIGNANT PROGRESSION IN LOW-GRADE GLIOMA PATIENTS
Study
EGAS00001002368
-
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Study
EGAS00001002202
-
Transcriptional_analysis_of_cells_from_lungs
Study
EGAS00001002649
-
Identification_of_immune_mechanisms_associated_with_the_high_rate_of_relapse_in_patient_with_visceral_leishmaniasis_and_HIV_co_infection
Study
EGAS00001003465
-
ChIP-seq of GOF p53 mutants
Study
EGAS00001002463
-
RNA-sequencing of gluten-reactive and non-reactive T-cells from blood samples of treated CeD patients during a gluten-challenge
Study
EGAS00001004988
-
Germline alterations of acute myeloid leukemia
Study
EGAS00001002760
-
H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
-
Osteosarcoma mate-pair and RNA-sequencing
Study
EGAS00001003842
-
The mutational landscape of primary central nervous system lymphoma (Hipo H050, A050, XD013)
Study
EGAS00001005339
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
Study
EGAS00001005457
-
Copy number analysis by SNP array
Study
EGAS00001005125
-
ImmunoAgeing_Longitudinal
Study
EGAS00001003183
-
scRNA-seq data of BALF and blood cells from COPD and control
Study
EGAS00001004369
-
Whole genome sequencing based on short and long reads from GM09237 cell line with and without folate depletion
Study
EGAS00001005345
-
A transcriptome atlas of human skeletal muscles
Study
EGAS00001005904
-
Cancer and germline exomes, and cancer RNA-seq consisiting of FASTQ paired-end reads from melanoma, lung and colon cancer samples
Study
EGAS00001005513
-
Genomic profiling of Follicular thyroid adenomas and carcinomas using exome-sequencing analyses
Study
EGAS00001005561
-
Multi-region whole-exome sequencing of 10 neuroblastoma cases
Study
EGAS00001004735
-
Human and rat skeletal muscle multi-omic profiling
Study
EGAS00001005730
-
CUT&RUN of AML1-ETO binding occupancy following miR-130a KD in Kasumi-1 cells
Study
EGAS00001005867
-
Gene_regulation_of_human_CD4__Treg_cells_
Study
EGAS00001003516
-
Placebo-only arm transcriptomic analysis of the phase 3 PROTECT clinical trial
Study
EGAS00001006344
-
Chromatin accessibility changes in hiPSC-derived neurons after BDNF and KCl stimulations
Study
EGAS00001006394
-
Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature
Study
EGAS00001006457
-
High-resolution lung adenocarcinoma expression subtypes identify tumors with dependencies on MET, CDK4, CDK6, and PD-L1
Study
EGAS00001006461
-
Human adipose tissue immune cells
Study
EGAS00001003725
-
cfDNA in Hereditary And High-Risk Malignancies (CHARM)
Study
EGAS00001006539
-
Y90 radioembolization followed by intravenous Nivolumab for advanced hepatocellular carcinoma
Study
EGAS00001006834
-
Pharmacogenomic profiling reveals molecular features of chemotherapy resistance in IDH wild type primary glioblastoma
Study
EGAS00001006989
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007052
-
Accuracy and repeatability of epigenome-based signatures trained on Illumina MethylationEPIC BeadChip data
Study
EGAS00001007184
-
scRNA-seq and scTCR-seq data IMCISION
Study
EGAS00001007368
-
Whole Genome sequencing of Angolan and Mozambican individuals
Study
EGAS00001007458
-
Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups
Study
EGAS00001007580
-
The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals
Dataset
EGAD00001008538
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015455
-
Pediatric Patient-Derived-Xenograft development in MAPPYACTS – international pediatric cancer precision medicine trial in relapsed and refractory tumors
Dataset
EGAD00001011048
-
Genomic Advances in Sepsis (GAinS) genotyping
Dataset
EGAD00001015369
-
Genomics of acral lentiginous melanoma
Dataset
EGAD00001010126
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015457
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015456
-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
Analyzing the expression profiles of genes in ureters with and without indwelling stents using RNAseq
Study
EGAS00001006855
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
-
Development and Validation of a Disability Severity Index for Charcot-Marie-Tooth Disease (CMT)
Study
phs001295
-
NICHD Genomic and Proteomic Network for Preterm Birth Research (GPN)
Study
phs000714
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK): Identification of VUR genes by exome sequencing
Study
phs000778
-
Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea
Study
phs001352
-
Exome Sequencing of Statin-Induced Myopathy Cases
Study
phs001342
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
Effect of Breast Feeding on Immunologic Priming in Young Infants
Study
phs002073
-
Temporal Lobe Epilepsy and Retrotransposons
Study
phs002067
-
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Study
phs001222
-
Exploring the Genetic Variants Associated with Brain Growth in Children
Study
phs000962
-
Genetics and Functional Studies of Autosomal Recessive Neurological Disorders
Study
phs003298
-
Integrating Genomic and Transcriptomic Data to Identify Breast Cancer Susceptibility Genes
Study
phs003535
-
Parallel Genomic Alterations of Antigen and Payload Targets Mediate Polyclonal Acquired Clinical Resistance to the Antibody Drug Conjugate Sacituzumab Govitecan
Study
phs002555
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Gabriella Miller Kids First Pediatric Research Program in Pediatric T-Cell Acute Lymphoblastic Leukemia
Study
phs002276
-
Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
Study
JGAS000052
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Genomic analysis of patient-derived xenograft models reveals intratumor-heterogeneity in endometrial cancer and can predict tumor growth inhibition with talazoparib
Study
EGAS00001004666
-
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
Scottish High Grade Serous Ovarian Cancer
Study
EGAS00001004410
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
-
HCA_Thymus_Disease_DiGeorge_Transplant_RNA
Study
EGAS00001004025
-
High-resolution testing of ctDNA dynamics predicts survival in metastatic NSCLC
Study
EGAS00001006703
-
Influence of Genomic Landscape on Cancer Immunotherapy for Newly Diagnosed Ovarian Cancer: Biomarker Analyses from the IMagyn050 Randomized Clinical Trial
Study
EGAS00001006838
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions(H021/INF)
Study
EGAS00001006939
-
ACT-Discover: identifying karyotype heterogeneity in pancreatic cancer evolution using ctDNA
Study
EGAS00001007077
-
Transcriptome of CD4+ T cells and CD8+ T cells in glioblastoma multiforme
Dataset
EGAD50000000226
-
Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort
Study
phs000372
-
Nala TAS-LRS PGx Study
Study
EGAS50000001116
-
Osteosarcoma 3D patient derived cultures to test genome-informed personalized treatment options; a feasibility study
Study
EGAS50000001583
-
Novel CNV contribution to schizophrenia from a genome wide study of 41,321 subjects
Study
EGAS00001001960
-
RNA-sequencing of human skin samples obtained from SSc patients and healthy controls.
Dataset
EGAD00001003832
-
PAK4 inhibition improves PD-1 blockade immunotherapy
Study
phs001919