-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Study
EGAS00001003846
-
SARS-CoV-2 escapes CD8 T cell surveillance via mutations in MHC-I restricted epitopes [10x]
Study
EGAS00001005060
-
Hepatitis B virus integrations promote local and distant oncogenic driver alterations in hepatocarcinogenesis
Study
EGAS00001004629
-
Deciphering somatic mosaic structural variation in human blood lineages using single-cell multiomics
Study
EGAS00001006567
-
Field effect of healthy and diseased livers (2019-04-08)
Dataset
EGAD00001004941
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma RNA
Dataset
EGAD00001014790
-
Single-cell profiling of neoantigen-specific T cells in lung cancers treated with neoadjuvant PD-1 blockade
Study
EGAS00001005343
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma WES
Dataset
EGAD00001014787
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma WES
Dataset
EGAD00001014789
-
Women's Health Initiative Clinical Trial and Observational Study - Imaging
Study
phs003824
-
Exome sequencing in patients with Calcific Aortic Valve Stenosis
Dataset
EGAD00001000053
-
Multi-omics analysis of pre-invasive lung adenocarcinoma in never-smokers
Dac
EGAC50000000385
-
UMCG Immunogenetics DAC
Dac
EGAC50000000785
-
Neurodegenerative_TGS
Study
EGAS00001002431
-
genome-wide cfDNA methylation analysis
Study
EGAS00001003958
-
H3K4me3, IgG, and Input ChIP-seq in overexpression of pLV Control, CS-FL and CS-ΔEx4 in SW1116 cells.
Study
EGAS00001008121
-
Plasma DNA profile in DNASE1L3 deficiency
Dataset
EGAD00001006216
-
Sanger sequencing of catalytic-domain encoding exons of tyrosine kinase genes from human endometrial tumor DNAs
Study
phs000841
-
Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation
Study
phs001512
-
Whole Genome Profiling to Detect Schizophrenia Methylation Markers
Study
phs000608
-
The Natural History of Mucolipidosis Type IV
Study
phs001329
-
Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)
Study
phs001350
-
Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000895
-
Orofacial Pain: Prospective Evaluation and Risk Assessment (OPPERA)
Study
phs000761
-
Generation of a Cellular Atlas of Human Adipose Tissue
Study
phs002766
-
Single cell sequencing of breast cancer T cells reveals a tissue-resident memory subset associated with improved prognosis
Study
EGAS00001002845
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Single_Cell_Sequencing_of_Sperm__scSperm_
Study
EGAS00001000935
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels
Study
EGAS00001003239
-
Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
-
WXS and RNA-seq for 22 patients treated with radiation + immunotherapy
Study
EGAS00001006212
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Diverse_outcomes_of_controlled_human_malaria_infection_originate_from_host_intrinsic_immune_variation_and_not_var_gene_switching
Study
EGAS00001003766
-
Acquired Copy Number Alterations in Adult Acute Myeloid Leukemia Genomes
Study
phs000201
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Coronary Artery Risk Development in Young Adults (CARDIA)
Study
phs000236
-
Elucidating Transcription Regulation by Epigenetics in Neuroblastoma
Study
phs001831
-
Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II)
Study
phs002386
-
Cardiovascular Health Study (CHS) Cohort: an NHLBI-funded observational study of risk factors for cardiovascular disease in adults 65 years or older
Study
phs000287
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021)
Study
EGAS00001002441
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer
Study
EGAS00001004935
-
Genetic Analysis of Normal Human Facial Variation
Study
phs000949
-
Mucociliary Clearance Consortium (MCC) Rare Genetic Disorders of the Airways: Cross-section Comparison of Clinical Features, and Development of Novel Screening and Genetic Test
Study
phs000595