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National Heart, Lung, and Blood Institute (NHLBI) Heart Healthy Lenoir (HHL) Genomics Study
Study
phs001471
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Adoptive Cell Therapy of Autologous T cell Receptor-Engineered T Cells Targeting the p53 Neoantigens in Human Solid Tumors
Study
phs002928
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Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology
Study
phs000814
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Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency
Study
phs000776
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The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia
Study
phs002297
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Adolescent Idiopathic Scoliosis (AIS) 1000 Exomes Study
Study
phs001677
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NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)
Study
phs001402
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The Mutational Landscape of CTCL and Sezary Syndrome
Study
phs000994
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Analysis of Epigenomes and Genome Topology in Colorectal Cancer
Study
phs002288
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Gabriella Miller Kids First Pediatric Research Project in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth Defects
Study
phs002174
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Normal Pressure Hydrocephalus
Study
phs002296
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Acute Respiratory Distress Network (ARDSNet) Study 02 Late Steroid Rescue Study (LaSRS) (ARDSNet-LaSRS-BioLINCC)
Study
phs003769
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Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis
Study
EGAS50000000753
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Gene expression adaptation of metastases to their host tissue
Study
EGAS50000000817
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Characterization of High-Grade Serous Ovarian Cancer Subtypes via Single-Cell and Spatial-Transcriptomics Profiling
Study
phs002262
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Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer
Study
EGAS50000000923
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Response to Tagraxofusp in Blastic Plasmacytoid Dendritic Cell Neoplasm
Study
phs003895
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Plasma cell‐Free transcriptome profiling in chronic liver disease
Study
EGAS50000000545
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Identification and Characterization of Cancer Mutations in Japanese LungAdenocarcinoma without Sequencing of Normal Tissue Counterparts
Study
JGAS000001
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Immuno-genomic Profiling of Biopsy Specimens Predicts Neoadjuvant Chemotherapy Response in Esophageal Squamous Cell Carcinoma
Study
JGAS000535
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Broad utility of ultrasensitive analysis of ctDNA dynamics across solid tumors treated with immunotherapy
Study
EGAS50000001333
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Human lymphoid-neutrophil/monocyte restriction co-ordinately activates increased proliferation despite parallel heterogeneity in transcriptional changes
Study
EGAS50000000278
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Fragmentomics Uncover Non-Mutational HRD Features
Study
EGAS00001008190
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Djerroudi et al., E-cadherin inactivation shapes tumor microenvironment specificities in invasive lobular carcinoma
Study
EGAS50000000761
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Reading about genomic analysis of pan-neuroblastoma
Blog
genomic-analysis-of-pan-neuroblastoma
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Genomic Analyses Identify Recurrent MEF2D Fusions in Acute Lymphoblastic Leukemia
Study
EGAS00001001952
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Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency
Study
EGAS00001002200
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Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
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DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
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Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
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DERMATLAS__Hidradenoma_papilliferum_WES
Study
EGAS00001005714
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DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
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DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
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Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Study
EGAS00001006218
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Ovarian cancer organoid biobank
Study
EGAS00001003073
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Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
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Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Study
EGAS00001002217
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Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
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DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
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DERMATLAS__Poroma_WES
Study
EGAS00001007705
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DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
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Field_effect_of_healthy_and_diseased_livers
Study
EGAS00001002382
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BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
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ALPI deficiency causes refractory Inflammation Bowel Disease
Study
EGAS00001003350
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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Study
EGAS00001001112
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Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
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Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Study
EGAS00001005023
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Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
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The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
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Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106