-
ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells.
Study
EGAS00001002983
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
DNA methylation analysis on PBL obtained from male patients with UC-PSC, UC and HC
Study
EGAS00001005832
-
Single_cell_characterization_of_T_cell_lymphoma_
Study
EGAS00001005750
-
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Study
EGAS00001003497
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Study
EGAS00001003973
-
Whole-genome sequencing of normal Singaporean volunteers
Study
EGAS00001004007
-
Single cell transcriptomics in expanded Tregs of APS-1 patients
Study
EGAS50000000181
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC)
Study
phs002068
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Study
phs000774
-
Systolic Blood Pressure Intervention Trial (SPRINT-BioLINCC)
Study
phs003483
-
Resuscitation Outcomes Consortium (ROC) Hypertonic Saline (HS) Trial Shock Study and Traumatic Brain Injury Study (TBI) (ROC-HS/TBI-BioLINCC)
Study
phs003777
-
Acute Respiratory Distress Network Early Versus Delayed Enteral Feeding to Treat People with Acute Lung Injury or Acute Respiratory Distress Syndrome (ARDSNet EDEN-BioLINCC)
Study
phs004168
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD-BioLINCC)
Study
phs003551
-
Incentives and Case Management to Improve Cardiac Care: Healthy Lifestyle Program (HeLP)
Study
phs003737
-
The Familial Intracranial Aneurysm Linkage Study (FIA)
Study
phs000293
-
NIDDK IBD Genetics Consortium Crohn's Disease Genome-Wide Association Study
Study
phs000130
-
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Study
phs000345
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – Whole exome sequencing
Study
EGAS00001004832
-
OpACIN-neo – A Multicenter Phase 2 Study to identify the Optimal neo-Adjuvant Combination scheme of Ipilimumab and Nivolumab – RNA sequencing
Study
EGAS00001004833
-
Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea
Study
phs001260
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
The Genomic Landscape of Mongolian Hepatocellular Carcinoma
Study
phs002000
-
CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population
Study
phs002324
-
Heart Failure Network Aldosterone Targeted Neurohormonal Combined with Natriuresis Therapy - (HFN ATHENA-BioLINCC)
Study
phs003506
-
Pathogenesis and Immunity in Endemic Burkitt Lymphoma
Study
phs001282
-
Sickle Cell Disease Natural History Data Resource (SCD NHDR)
Study
phs003529
-
Exploratory novel biomarker and resistance mechanism of milademetan, an MDM2 inhibitor, in MDM2 amplified intimal sarcoma from an open-label phase 1b/2 trial ���NCCH1806/MK004���
Study
JGAS000619
-
Geisinger Health System - MyCode, eMERGE III Exome Chip
Study
phs000957
-
High-throughput single-cell DNA sequencing of acute myeloid leukemia tumors with droplet microfluidics
Study
phs001627
-
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Study
phs001658
-
Identification of Genes Involved in Familial Coronary Artery Disease
Study
phs000514
-
Gene Expression Analysis in Clonal Evolution of Fanconi Anemia
Study
phs003024
-
The Genomic Complexity of Primary Human Prostate Cancer
Study
phs000330
-
Genetic Determinants of Susceptibility to Severe COVID-19 Infection
Study
phs002245
-
Left Atrial Cardiomyocyte Transcriptomic Analysis of Postoperative Atrial Fibrillation
Study
phs003644
-
Exome Sequencing in an Ancestrally Diverse Autism Cohort
Study
phs003603
-
Integrating Circulating Tumor DNA Analysis and Radiomics for Dynamic Risk Assessment in Localized Lung Cancer
Study
phs003947
-
Identifying the Genetic Basis of Variably Protease-Sensitive Prionopathy (VPSPr)
Study
phs004012
-
Transcriptome analysis of kidney organoids lacking NPHP1gene
Study
JGAS000683
-
Elucidating the development of cervical cancer and identifying therapeutic targets based on cancer genome analysis.
Study
JGAS000803
-
Reference Panel for Imputation Analysis Based on Whole Genome Sequencing Data of 3,256 Japanese Individuals(BioBank Japan genotype data)
Study
JGAS000746
-
Spatial transcriptome analysis of aging of healthy skin samples
Study
JGAS000771
-
Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors .
Study
JGAS000737
-
The Adhesion GPCR ADGRL2 Engages Galpha13 to Enable Epidermal Differentiation
Study
phs004223
-
Whole blood transcriptomics analysis in Antiphospholipid syndrome in patients with Systemic Lupus Erythematosus
Study
EGAS00001007750
-
Khoe-San genome Project (KSGP)
Dac
EGAC50000000798
-
Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors .
Study
JGAS000303
-
Analysis of genes related to the oncogenesis, progression or effectiveness of drug therapies of urological tumors .
Study
JGAS000564
-
Microarray genotyping of idiopathic hypersomnia patients (11 orexin mutation-positive patients, 85 orexin mutation-negative patients)
Study
JGAS000508
-
Mechanisms on relapse after allogeneic hematopoietic cell transplantation in CMML
Study
JGAS000317
-
Cancer genomics for elucidation of molecular mechanisms of carcinogenecis and progression in lung cancer
Study
JGAS000756
-
Genome-wide copy number analysis of neuroblastoma
Study
JGAS000046
-
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
Study
EGAS00000000054
-
Complex Landscapes of Somatic Rearrangements in Human Breast Cancer Genomes
Study
EGAS00000000062
-
Lung_Rearrangement_Study
Study
EGAS00001000005
-
ER___HER2___PR__breast_Cancer_genome_sequencing
Study
EGAS00001000197
-
Single-cell profiling reveals monocyte mitochondrial dysfunction in patients with cirrhosis progressing to acute-on-chronic liver failure
Study
EGAS50000001127
-
A new subgroup of hepatocellular adenomas with sonic hedgehog pathway activation
Study
EGAS00001002091
-
Mutagenic impact of radiotherapy in B-cell lymphoma and multiple myeloma
Study
EGAS50000000997
-
Whole-genome sequencing in gastric cancer (part2)
Study
EGAS00001006575
-
Defective homologous recombination in HCC
Study
EGAS00001006599
-
RNAseq on 20 samples of multiple myeloma patients and 3 normal plasma cells.
Study
EGAS00001004347
-
Clonal hematopoiesis in rheumatoid arthritis
Study
EGAS50000000890
-
The Berlin (BLN) panel of glioblastoma cell lines: RNAseq of human gliomasphere cell lines and matched parental tumors
Study
EGAS00001001167
-
Determining off-target effects of splice-switching antisense oligonucleotides using short read RNAseq in neuronally differentiated human induced pluripotent stem cells
Study
EGAS50000001222
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Whole-genome and transcriptome sequencing of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
Study
EGAS00001004332
-
Circulating cell-free DNA methylation profiling for detection, distinction, and estrogen receptor status classification of advanced breast cancer
Study
EGAS50000001675
-
CLL_Cancer_Whole_Genome_Sequencing
Study
EGAS00001000014
-
TMD_AMLK_Exome_Study
Study
EGAS00001000027
-
μSeq: Universal mutation rate quantification via deep sequencing of a single clonal expansion
Study
EGAS50000001761
-
Burden_of_Disease_in_Sarcoma
Study
EGAS00001000087
-
Deciphering the mutational landscape and the genome organization of LMS
Study
EGAS00001001262
-
Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Whole-Genome Sequencing of 128 Ashkenazi Jewish individuals
Study
EGAS00001000664
-
Molecular profiling of MBD4-deficient acute myeloid leukaemia
Study
EGAS00001002581
-
Whole genome sequencing data of paediatric ETV6::RUNX1 acute lymphoblastic leukemia
Study
EGAS50000001599
-
RNA-sequençing of 21 inflammatory hepatocellular adenomas
Study
EGAS00001003685
-
Bulk-mRNA sequencing comparing hiPSC derived vascular cells from CADASIL patient lines
Study
EGAS50000001507
-
Grey_Platelet_Syndrome__GPS_
Study
EGAS00001000091
-
Population_sequencing_phasing
Study
EGAS00001001852
-
Primary_Lung_Cancer_whole_genome_study
Study
EGAS00001000354
-
ICGC_Benchmarking_Exercise
Study
EGAS00001000433
-
Reconstruction of human terminal erythroid differentiation cell at single cell level
Study
EGAS00001003114
-
Patient-derived organoids as predictive models for drug testing and repurposing in glioblastoma therapy
Study
EGAS50000001221
-
RNA sequencing to characterize ALK
Study
EGAS50000001779
-
Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
-
WGS___Mutant_clone_mapping_in_normal_oesohagus_and_skin
Study
EGAS00001002416
-
The_International_1q_type_2_diabetes_consortium
Study
EGAS00001000062
-
Capture Hi-C on MM
Study
EGAS00001002614
-
Ultra-fast multiplex small DNA sequencing on the MinION nanopore sequencing platform
Study
EGAS00001002650
-
Cancer_Exome_Resequencing
Study
EGAS00001000206
-
Investigating_the_impact_of_MBD4_on_the_mutability_of_the_germline
Study
EGAS00001002861
-
Breast_Cancer_Exome_Sequencing
Study
EGAS00001000211