-
A Randomized, Double-Blind, Crossover Study of Sodium Phenylbutyrate (Buphenyl) and Low-Dose Arginine (100 mg/kg/day) Compared to High-Dose Arginine (500 mg/kg/day) Alone on Liver Function, Ureagenesis and Subsequent Nitric Oxide Production in Patients with Argininosuccinic Aciduria (ASA)
Study
phs001305
-
Neutrophils and emergency granulopoiesis drive immune suppression and an extreme response endotype during sepsis DAC
Dac
EGAC00001003275
-
DAC Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Dac
EGAC00001002978
-
Liquid Biopsy Versus Tissue Biopsy to Assess Acquired Resistance and Tumor Heterogeneity in Gastrointestinal Cancers
Study
phs001853
-
NHLBI TOPMed: Defining the Time-Dependent Genetic and Transcriptomic Responses to Cardiac Injury Among Patients with Arrhythmias
Study
phs001434
-
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Study
phs001675
-
PCPT and SELECT Cohorts: Core Infrastructure Support for Cancer Research
Study
phs003382
-
Sequencing and analysis of a South Asian-Indian personal genome
Study
EGAS00001000328
-
C3 SNPs and outcome after lung transplantation
Study
EGAS00001003843
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
Sporadic and endemic Burkitt lymphoma have frequent FOXO1 mutations but distinct hotspots in the AKT recognition motif
Study
EGAS00001003719
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
Study of Environment, Lifestyle and Fibroids SNP Data
Study
phs002513
-
Idiopathic Pulmonary Fibrosis Network (IPFnet) Prednisone, Azathioprine, and N-Acetylcysteine: A Study That Evaluates Response in Idiopathic Pulmonary Fibrosis (IPFNet-Panther-IPF-BioLINCC)
Study
phs004071
-
Better Outcomes for Children: GWAS from Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase II data - (dbGaP Deposit 1)
Study
phs000494
-
dbGaP Collection: NHLBI Heart Failure Related dbGaP Data (No IRB requirement)
Study
phs001991
-
CIDR: NINDS High Throughput Genotyping Resource Access for Structural Hindbrain Disorders
Study
phs002621
-
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Study
phs000308
-
Study on longer adjuvant chemotherapy in Women with Early Breast Cancer
Study
phs000807
-
Study of Leukemia Stem Cells in B-ALL
Study
phs002492
-
Genomic Analysis of Metastatic Brain Cancer
Study
phs002639
-
The Placenta Harbors a Unique Microbiome
Study
phs000735
-
Bulk RNA Sequencing of 86 Human Donor Lungs
Study
phs002484
-
Integrative Tissue Analysis of Men with Prostate Cancer
Study
phs001813
-
E05-Bioenvironmental Psychiatry
Dac
EGAC50000000222
-
Personalized Breast Cancer Vaccines Based on Genome Sequencing
Study
phs002787
-
Molecular profiling of HGBCL-DH-BCL2 patients treated in the HOVON-152 trial
Study
EGAS50000001453
-
Whole genome sequencing of preneoplasia lung adenocarcinoma
Study
EGAS50000000272
-
3D chromatin analysis of clear cell renal cell carcinoma using micro-C
Study
EGAS50000001323
-
Identification of genetic etiology of CAMRQ2
Study
EGAS00000000099
-
ICARUS-BREAST01-ExomeSeq
Study
EGAS50000000542
-
ICARUS-LUNG01-RNAseq
Study
EGAS50000000732
-
Transrenal DNA Analysis
Study
EGAS50000000766
-
CRISPRi/a of GATA2/NR4A2/SOX17 upon spontaneous iPSC differentiation
Study
EGAS50000000819
-
RNA-seq and ATAC-seq data for ex vivo expanded T cells
Dataset
EGAD50000002471
-
Single-Cell DNA and Protein Sequencing Data from a Pediatric UBA1-Mutated MDS Patient
Dataset
EGAD50000002372
-
Raw and processed Spatial Transcriptomics data of Choroid Plexus Tumours
Dataset
EGAD50000002319
-
Single-cell RNA sequencing of Small Intestinal Neuroendocrine Tumors (SI-NET)
Dataset
EGAD50000002265
-
RNA-seq after drug perturbation of primary lymphoma samples
Dataset
EGAD50000002166
-
Small RNA-Seq of MicroRNA's in extracellular vesicles of Ushers Syndrome patients
Dataset
EGAD50000001709
-
WGS Data from 42 Multi-Region Sampled IPMN-PDACs and 12 Matched Normal Samples
Dataset
EGAD50000001687
-
Genetic data of a monozygotic twin pair discordant for ALS
Dataset
EGAD50000001329
-
Total RNA-seq of CRPC and NEPC
Dataset
EGAD50000001312
-
RNA-seq data of proliferative vitreoretinal diseases and healthy human retinal pigment epithelium
Dataset
EGAD50000001780
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (Owen)
Dataset
EGAD50000001212
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Stockholm, Sweden (Pedersen)
Dataset
EGAD50000001026
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from London, UK
Dataset
EGAD50000000950
-
WES of Bipolar cases and controls performed at the Broad Inst on cohort from Cardiff, UK (Craddock)
Dataset
EGAD50000000547
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (O'Donovan)
Dataset
EGAD50000000887
-
Whole transcriptome sequencing of pheochromocytoma and paraganglioma arising from germline SDHB mutations
Dataset
EGAD50000000504
-
Genomic and Transcriptomic sequencing of neuroblastoma patient
Dataset
EGAD50000000728
-
Whole transcriptome sequencing data of 3 histiocytic tumors with CLTC::SYK fusions
Dataset
EGAD50000000834
-
Single-cell multi-omic analysis of control and glioblastoma samples from the brain and border regions.
Dataset
EGAD50000000045
-
Valid reads
Dataset
EGAD00001006486
-
Genomic analysis of seminomas
Study
EGAS00001000943
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
Screening of 2.5 million SNPs in 142 samples from the western Mediterranean area
Study
EGAS00001003901
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
Resistance_to_MAPK_inhibitor_induces_internal_duplication_in_BRAF
Study
EGAS00001001304
-
SNU_WGS_AML
Study
EGAS00001001906
-
ORCADES_WGA
Study
EGAS00001000068
-
RE_NanoSeq___TwinsUK_Buccal
Study
EGAS00001007740
-
RNAseq_of_patients_with_Ewings_sarcoma
Study
EGAS00001000267
-
Ewings_Sarcoma_Rearrangement_Screen
Study
EGAS00001000362
-
HipSci_RNASEQ_Spastic_paraplegia
Study
EGAS00001001991
-
Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Landscape of gene mutations in Down syndrome-related myeloid disorders
Study
EGAS00001000546
-
Somatic_Variation_Angiosarcoma
Study
EGAS00001002610
-
HipSci_RNASEQ_Kabuki
Study
EGAS00001001989
-
SNU_PROSPECTIVE
Study
EGAS00001002154
-
Pre_clinical_evolution_of_haematological_malignancies
Study
EGAS00001002964
-
Exome_sequencing_of_patients_with_Ewings_sarcoma_
Study
EGAS00001000266
-
Myeloproliferative_Neoplasms__MPN__Targeted_Gene_Screen
Study
EGAS00001000406
-
Integrative and comparative genomic analyses identify clinically relevant groups of pulmonary carcinoids and unveil the supra-carcinoids
Study
EGAS00001003699
-
ESGI___Whole_Genome_Sequencing_of_samples_from_the_ORCADES_cohort__X10__
Study
EGAS00001001125
-
HipSci_RNASEQ_Retinitis_Pigmentosa
Study
EGAS00001001996
-
CD4+ T cell subsets stratified by complement receptor type 2 (CR2) expression
Study
EGAS00001001870
-
Genome-wide association data on male-pattern baldness
Study
EGAS00001001354
-
Genome-wide data from Agta hunter-gatherers in Philippines
Study
EGAS00001005315
-
Whole-genome low pass sequencing of 3,514 Sardinian individuals
Study
EGAS00001002212
-
PROJET DREPANOCYTOSE ET PALUDISME
Study
EGAS00001006008
-
Transcriptomic analysis of TFEB knockdown in LT-HSC.
Study
EGAS00001004967
-
Advanced molecular neuropathology to increase diagnostic accuracy in pediatric neurooncology
Study
EGAS00001006680
-
Nasal Polyp RNAsequencing, Skaraborg Sweden
Study
EGAS00001007088
-
ATAC-seq dataset of patient and healthy donors
Dataset
EGAD00001008370
-
Whole exome data from PMID27216186
Dataset
EGAD00001008149
-
Single-cell Transcriptomic and Immune Receptor Profiling of PBMCs from Dengue-Infected Individuals with Varying Disease Severities
Dataset
EGAD00001015634
-
Personalized Medicine Based on Genomic Data
Study
JGAS000874
-
Whole genome sequences and variant calls from human cells exposed to UV and CX5461
Dataset
EGAD50000001640
-
The spatial organization of intratumor heterogeneity and evolutionary trajectories of metastasis in hepatocellular carcinoma
Dataset
EGAD00001003138
-
ChIP-Seq on multiple myeloma and plasma cell leukaemia cell lines
Dataset
EGAD00001003349
-
Mitochondrial DNA (mtDNA) sequences from subjects with intellectual disability (ID) and austism spectrum disorder (ASD)
Dataset
EGAD00001004213
-
Patient-derived neuroblastoma model system OHC-NB1
Dataset
EGAD00001004138
-
TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors
Dataset
EGAD00001001635
-
Exome sequencing of Congenital Heart Disease families from the Competence Network Berlin
Dataset
EGAD00001000800