-
Role of Genetic Factors in the Pathogenesis of Lung Disease
Study
phs003108
-
Fibroblast heterogeneity and immunosuppressive environment in Human breast cancer
Study
EGAS00001002508
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000850
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000794
-
Analysis of Somatic Mutations in Pediatric AML FAB-M7 Subtype by Whole Transcriptome Sequencing
Study
phs000413
-
High Frequency Ventilation in Premature Infants (HIFI-BioLINCC)
Study
phs004032
-
Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
-
Genomic Analysis of Pediatric Low Grade Gliomas
Study
phs000614
-
The Dynamic Immune Behavior of Primary and Metastatic Ovarian Carcinoma
Study
EGAS50000000038
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
Study
EGAS00001005878
-
Targeting TRIP13 in Wilms Tumor with Nuclear Export Inhibitors
Study
EGAS00001007389
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma
Study
EGAS00001005986
-
Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples and cell lines.
Study
EGAS00001000736
-
Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma
Study
EGAS00001002811
-
RNA-seq of M-CSF differentiated human peripheral monocyte-derived macrophages (MDMs) - Validation macIDR
Study
EGAS00001003451
-
Human NXPE1 mediates variation in sialic acid O-acetylation in Colon Tissue
Study
EGAS00001007704
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): REasons for Geographic and Racial Differences in Stroke (REGARDS)
Study
phs002919
-
Gene Variants in Pheochromocytoma and Paraganglioma
Study
phs002405
-
Cholesterol homeostasis and lipid raft dynamics at the basis of tumor-induced immune dysfunction in chronic lymphocytic leukemia
Dac
EGAC50000000556
-
P4HA1 Mediates Hypoxia-Induced Invasion in Human Pancreatic Cancer Organoids
Study
phs003961
-
Spatial atlas of clonal copy number alterations in co-existing benign and malignant tissue
Study
EGAS00001006124
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
GWAS in bullous pemphigoid in Germans
Study
EGAS00001004627
-
Analysis of chromosomal background of cancerous mutations using a long-read sequencer
Study
JGAS000349
-
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WGS
Study
EGAS00001002658
-
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES
Study
EGAS00001002842
-
Transcriptome profiling for Korean Diffuse Gastric cancers
Study
EGAS00001001859
-
Bone marrow derived stromal cells from Myelodysplastic Syndromes
Study
EGAS00001005051
-
Whole-Exome Sequences from Imazighen and non-Imazghen from Algeria
Study
EGAS00001007236
-
IκBε deficiency accelerates disease development in chronic lymphocytic leukemia
Dataset
EGAD50000000754
-
Heritable pulmonary arterial hypertension - new genetic findings and environmental triggers
Study
EGAS50000001275
-
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
Study
EGAS00001002334
-
Metabolic context regulates the competitive fitness of oncogenic PIK3CA mutant clones in the normal esophagus
Dataset
EGAD00001008281
-
Cohesin Mutations in AML
Study
EGAS00001007405
-
Mobile Technology to Identify Mechanisms Linking Genetic Variation and Depression in Intern Health Study (IHS)
Study
phs001826
-
The MALT1 Locus and Peanut Avoidance in the Risk for Peanut Allergy
Study
phs001851
-
Low T cell diversity is associated with poor outcome in bladder cancer - Single cell RNAseq and TCRseq data
Study
EGAS50000000938
-
Immune control of functional memory CD8 T cells in normal-appearing vitiligo skin
Study
EGAS50000001317
-
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Study
EGAS00001002352
-
Circulating tumor cell copy-number heterogeneity in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors
Study
EGAS00001005301
-
Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy
Study
EGAS00001005398
-
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Study
EGAS00001004682
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
Complex structural variation patterns in pediatric solid tumors
Study
EGAS00001007565
-
BRAIN Cell EncyclOpeDia of Transcribed Elements (BRAINcode)
Study
phs001556
-
WES of 2 human osteosarcoma and corresponding cell lines
Study
EGAS00001003923
-
Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas
Study
JGAS000284
-
Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA
Dataset
EGAD00001005071
-
Nasal Polyp Whole-transcriptome sequencing
Dataset
EGAD00001010146
-
Time Lapse to Cancer-Defining the Transition from Polyp to Cancer
Study
phs001384
-
Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses
Study
EGAS00001006660
-
Geographic and age-related variations in mutational processes in colorectal cancer - sequence data (Mutographs)
Dataset
EGAD00001015485
-
Molecular Determinants of Esophageal Cancer in Tanzania
Study
phs003217
-
DynaTag for efficient profiling of transcription factors in small samples and single cells
Study
EGAS50000001074
-
Onco-exaptation of an Endogenous Retroviral LTR Drives IRF5 Expression in Hodgkin Lymphoma
Study
EGAS00001001205
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
-
National Cancer Institute (NCI) Genome Wide Association Study (GWAS) of Lung Cancer in Never Smokers
Study
phs000634
-
Resistance to Checkpoint Blockade Therapy Through Inactivation of Antigen Presentation
Study
phs001427
-
A Missense SNP in the Tumor Suppressor SETD2 Reduces H3K36me3 and Mitotic Spindle Integrity in Drosophila
Study
phs003474
-
Enhancer profiling identifies epigenetic markers of endocrine resistance and reveals therapeutic options for metastatic castration-resistant prostate cancer patients (LuCaP cell line data)
Study
EGAS50000000917
-
Targeted Gene Panel for 171 PTCLs
Study
EGAS00001002740
-
Clonal Evolution of Pre-Leukemic Hematopoietic Stem Cells Precedes Human Acute Myeloid Leukemia
Study
phs000549
-
Genomic Studies for Understanding Etiology of Esophageal Adenocarcinoma (EsophagealAdenocarcinoma_Chinese)
Study
phs001696
-
Hi-C Profiling of Solid Tumor Samples
Study
phs003227
-
CLL Genome
Study
EGAS00000000092
-
Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease
Study
EGAS00001003751
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
A comprehensive characterization of the cell-free transcriptome reveals tissue- and subtype-specific biomarkers for cancer detection
Study
EGAS00001004704
-
TCR Repertoire Sequencing to Evaluate the Diversity of Follicular Helper T Cells in HIV Infected Lymph Nodes
Study
phs001548
-
Circulating RNAs in Acute Heart Failure (CRUCIAL)
Study
phs003403
-
Integrated Transcriptomic and Regulatory RNA Profiling Reflects Complex Pathophysiology and Uncovers a Conserved Gene Signature in End Stage Heart Failure RNA-Seq data
Study
EGAS50000000810
-
RNA-seq data of bone marrow CD34-positive cells from 57 patients with myelodysplastic syndromes (MDS) and 5 healthy individuals (62 participants in total)
Study
JGAS000724
-
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
-
SNP genotyping data in genes related to trace element homeostasis
Study
EGAS00001001292
-
Competitive selection of somatic mutant clones in normal human skin varies with body site
Dataset
EGAD00001006194
-
Germline Genetic Variants in Cancer-Susceptibility Genes in Patients with Osteosarcoma
Study
phs002444
-
Transcriptome analysis of Familial dysautonomia patient cells treated with splice-regulating compounds
Study
JGAS000170
-
Transcriptome analysis of Fabry disease iPSC-derived cardiomyocytes treated with splice-regulating compound; RECTAS
Study
JGAS000225
-
TBA
Study
EGAS00001000802
-
TBA
Study
EGAS00001000803
-
Loss of functional mutation in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan Anemia
Study
EGAS00001000875
-
TBA
Study
EGAS00001000801
-
RNAseq_of_Human_Organoid_Lines
Study
EGAS00001003888
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
Subtype specific studies of breast cancer progression. Milan cohort.
Study
EGAS00001004390
-
Mutational_burden_in_skin_following_UV_treatment_Nanoseq
Study
EGAS00001007681
-
Mutational_burden_in_skin_following_UV_treatment_WGS
Study
EGAS00001007682
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
The Intestinal Bacterial Metagenome in Pediatric Non-Alcoholic Fatty Liver Disease (NAFLD)
Study
phs001837
-
Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
-
'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
-
Characterization of Immune-Related Gene Expression in Lung Cancer
Study
phs002346
-
Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
-
Prevalence and association of microsatellite instability and Lynch syndrome Pan-Cancer and development of a personalized cancer risk prediction tool for Lynch syndrome carriers in India
Study
EGAS50000001449
-
A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi
Study
EGAS00001002075
-
Geographic and age-related variations in mutational processes in colorectal cancer - filtered vcf files (Mutographs)
Dataset
EGAD00001015486