-
InterPregGen-GWAS-KAZ-3
Dataset
EGAD00010001949
-
Transcriptomic changes in placenta associated with anesthesia, delivery mode and maternal diabetes
Study
EGAS50000000489
-
Mutagenic impact of radiotherapy in B-cell lymphoma and multiple myeloma
Study
EGAS50000000997
-
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214
-
Characterizing the immune and genome landscapes for osteosarcoma
Study
EGAS00001003247
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Pulmonary Arterial Hypertension)
Study
phs000290
-
Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions(H021/INF)
Study
EGAS00001006939
-
Enrichment of PTPRT and JAK2 mutations in lung cancer from African Americans and evidence for increased GI and HRD in LUSC
Study
phs001895
-
Integrative Genomic and Transcriptomic Analyses of Refractory Multiple Myeloma
Study
phs002498
-
NHLBI TOPMed: Children's Health Study (CHS) Integrative Genomics and Environmental Research of Asthma (IGERA)
Study
phs001603
-
Longitudinal Assessment of Methylmercury and Gut Microbes During Pregnancy
Study
phs001768
-
Single cell targeted DNA-sequencing (and antibody sequencing) of high hyperdiploid B-ALL
Dataset
EGAD50000000829
-
Sequencing of serial plasma and multiregional tumor samples in a patient with metastatic breast cancer
Study
EGAS00001001466
-
WGS of breast cancer diagnosed during pregnancy and matched control
Study
EGAS00001002685
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
CIDR Estrogen Receptor Negative Breast Cancer in African American Women: DNA Methylation, Reproductive Events, and Mammary Epithelial Cell Populations
Study
phs002688
-
DNA Methylation Characterization of Fusion-Positive and Fusion-Negative Rhabdomyosarcoma
Study
phs001970
-
Single-Cell ATAC and RNA Sequencing of Human Breast Cancer Reveals Salient Cancer-Specific Enhancers
Study
phs003253
-
Gliomas, glioneuronal and neuronal tumors
Dataset
EGAD50000000300
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
Genomic and immune profiling of pre-invasive lung adenocarcinoma
Study
EGAS00001004006
-
Combined – whole blood and skin fibroblasts - transcriptomic analysis in Psoriatic arthritis.
Study
EGAS00001006288
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Study
EGAS00001005268
-
Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067)
Study
EGAS00001004363
-
International Consortium to Identify Genes and Interactions Controlling Oral Clefts
Study
phs000094
-
NHLBI TOPMed: The Genetic Epidemiology of Asthma in Costa Rica
Study
phs000988
-
A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genes
Study
phs003348
-
Risk Factors for Asymptomatic Diverticulosis
Study
phs003556
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
Molecular pathways and cellular subsets associated with adverse clinical outcomes in overlapping immune-related myocarditis and myositis
Dataset
EGAD50000000488
-
SPEN loss drives extra-follicular diffuse large B cell lymphoma with female-specific lethality and TLR pathway therapeutic vulnerabilities
Study
EGAS50000001594
-
The Role of Myeloid Cells in Parkinson's Disease
Study
phs002400
-
The Genetic Basis of Hypodiploid ALL
Study
phs000341
-
Genomic Profiling of Melanoma
Study
phs000933
-
NHLBI TOPMed: MWCCS: Sex Differences in the Role of Multi-Omics in HIV-Associated Carotid Artery Atherosclerosis
Study
phs003651
-
Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer
Study
EGAS50000000297
-
INCLUDE: Down Syndrome Early Post-Natal Brain Multiome
Study
phs004098
-
Spatial Dynamics of the Developing Human Heart
Study
EGAS50000001122
-
Spatial Dynamics of the Developing Heart (single-cell)
Study
EGAS50000001029
-
EATL-II STUDY
Study
EGAS00001001879
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
SeqControl: Process Control for DNA Sequencing
Study
EGAS00001000899
-
Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing
Study
EGAS00001001736
-
Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Study
EGAS00001004723
-
The genomic landscape of cutaneous squamous cell carcinoma from immunosuppressed and immunocompetent patients reveals common drivers and a novel mutational signature associated with chronic azathioprine exposure
Study
EGAS00001002612
-
Using de novo assembly to identify structural variation of complex immune system gene regions
Study
EGAS00001005046
-
Novel paediatric case of a spinal high-grade astrocytoma with piloid features in a patient with Noonan Syndrome
Study
EGAS00001007937
-
WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001010135
-
WGS of high grade serous ovarian tumours and matched blood normals
Dataset
EGAD00001009049
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
ARHGAP11A Maintains Cortical Progenitor Identity Through RHOA–ROCK Signalling During Human Brain Development
Study
EGAS00001008322
-
Centers for AIDS Research (CFAR) Network of Integrated Clinical Systems (CNICS)
Study
phs001788
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899
-
Multi-Ethnic Study of Atherosclerosis (Electrocardiogram Tracing Repository)
Study
phs003703
-
Cancer-Restricted Cryptic Antigens Are Targets for T Cell Recognition
Study
phs003887
-
A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy
Study
EGAS50000000228
-
Host-microbe interactions in a novel SARS-CoV-2 human challenge model
Study
EGAS50000001440
-
Identification of putative multiple myeloma (MM) susceptibility genes
Study
EGAS50000001259
-
A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Dataset
EGAD50000001712
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Study
phs002094
-
Bone marrow breakout lesions act as key sites for tumor-immune cell diversification and exhaustion in multiple myeloma
Study
EGAS50000000304
-
Monocyte and macrophage lipid accumulation results in downregulated type-I interferon responses
Study
EGAS00001005955
-
Tamoxifen Response at Single Cell Resolution in Estrogen Receptor Positive Primary Human Breast Tumors
Study
phs003186
-
Prospective Procurement of Solid Tumor Tissue to Identify Novel Therapeutic Targets
Study
phs001003
-
Correlates of Human Nerve Repair
Study
phs001796
-
Epigenetic Damage in Women Living in LA Food-Desert Zip Codes
Study
phs003522
-
Elucidation of the association between viruses and autoimmune diseases and COVID-19
Study
JGAS000741
-
Analytical study of protein function and RNA expression involved in predicting treatment efficacy and adverse event development in lung cancer radiotherapy.
Study
JGAS000545
-
RNaseq of mantle cell lymphoma patient samples
Study
EGAS50000001086
-
Genomic landscape of aplastic anemia
Study
EGAS50000001516
-
Intratumor heterogeneity evaluation in primary HCC cells
Study
EGAS00001001135
-
Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes
Study
EGAS00001004165
-
Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans
Study
EGAS00001002736
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
scRNA-seq of total bone marrow mononuclear cells and CD3+ T cells of multiple myeloma patients and healthy donors
Study
EGAS00001006980
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015377
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015379
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015376
-
Chronic Renal Insufficiency Cohort (CRIC) Study Metabolomics and Proteomics
Study
phs003709
-
Mind Body Study: A Sub-Study on Psychosocial Factors and Microbiomes of Nurses in the Nurse's Health Study II
Study
phs003786
-
DynaTag for efficient profiling of transcription factors in small samples and single cells
Study
EGAS50000001074
-
TDP43 proteinopathy leads to divergent cryptic splicing in the cortex and spinal cord
Study
EGAS50000000575
-
Establishing stable brain tumor stem cell lines and translational research for new treatments
Study
JGAS000657
-
ARAF Mutations Confer Resistance to RAF Dimer Inhibitor Belvarafenib in NRAS- and BRAF- Mutant Melanoma
Study
EGAS00001005086
-
Neoantigen Landscape in a Hypermutated Glioblastoma Arising in a Patient with Germline POLE Deficiency Treated with Checkpoint Blockade Immunotherapy
Study
phs001663
-
CHEK2 molecular manuscript
Study
EGAS50000000080
-
Sanger sequencing analysis data using cfRNA from plasma samples in 6 cases, 10 samples, all from sarcoma.
Study
JGAS000787
-
Genome sequencing of biliary tract cancers
Study
JGAS000109
-
Genome sequencing of biliary tract cancers
Study
JGAS000389
-
RNAseq of Thymic epithelial tumors and paired normals
Dataset
EGAD50000001158
-
WES of thymic epithelial tumors and paired normals
Dataset
EGAD50000001159
-
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
Study
EGAS00001000878
-
Whole genome sequencing of Japanese HCCs
Study
EGAS00001000671