-
University of Texas PDX Development and Trial Center Grant
Study
phs001980
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells
Study
phs001205
-
Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic
Study
phs000942
-
Targeted Linked-Read DNA-seq Analysis of Castration-Resistant Prostate Cancers
Study
phs003343
-
Center for Sub-Cellular Genomics
Study
phs002120
-
Machine learning to detect the SINEs of cancer
Study
EGAS00001007169
-
Uncovering Inversion Formation in the Human Genome and its Impact to Disease
Study
phs002999
-
Biopsy-Derived Organoids in Personalised Early Breast Cancer Care: Challenges of Tumour Purity and Normal Cell Overgrowth Cap Their Practical Utility
Study
EGAS50000000605
-
Decoding Human Endogenous Retrovirus Expression in Liver Metastatic Colorectal Cancers: Implications for Diagnosis and Prognosis
Study
EGAS50000000307
-
Cancer-associated fibroblasts promote drug resistance in ALK-driven lung adenocarcinoma cells by upregulating lipid biosynthesis
Study
EGAS50000000135
-
Enhanced Adjuvanticity of a Personal Neoantigen Vaccine Generates Potent Neoantigen-Specific Immunity
Study
phs003919
-
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
-
HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium
Study
phs002267
-
Genomic landscapes of endometrioid and mucinous ovarian cancers and morphologically similar tumor types
Study
EGAS50000000523
-
CRISPR screening in human trophoblast stem cells reveals both shared and distinct aspects of human and mouse placental development
Study
JGAS000659
-
Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma
Study
JGAS000646
-
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
Study
JGAS000057
-
DNA methylation at HBV integrants and flanking host genomes
Study
JGAS000015
-
Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Study
EGAS00001002117
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Study
EGAS00001000476
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Evolution of the African pygmy phenotype
Study
EGAS00001000908
-
Bioinformatic Methods and Bridging of Assay Results for Reliable Tumor Mutational Burden Assessment in Non-Small Cell Lung Cancer
Study
EGAS00001003661
-
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Study
EGAS00001004467
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
-
Tissue-specific mutation accumulation in human adult stem cells during life
Study
EGAS00001001682
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry
Study
EGAS00001002678
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112
-
Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Study
EGAS00001003452
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01
Study
EGAS00001000249
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003138
-
Long-read trio sequencing of unsolved patients with intellectual disability
Study
EGAS00001004319
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Efficacy of JAK/STAT pathway inhibition in murine xenograft models of early T-cell precursor (ETP) acute lymphoblastic leukemia
Study
EGAS00001001146
-
The clonal and mutational evolution spectrum of primary triple negative breast cancers
Study
EGAS00001000132
-
Renal_habitat_WXS
Study
EGAS00001003703
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia
Study
EGAS00001003975
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
H3.3G34R/V-transformed interneuron progenitors co-opt PDGFRA for gliomagenesis
Study
EGAS00001004301
-
Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia
Study
EGAS00001004325
-
Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Study
EGAS00001004538
-
Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Study
EGAS00001003964
-
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
-
Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235
-
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Study
EGAS00001007555
-
WGS and WES data of invasive micropapillary carcinoma of breast
Dataset
EGAD00001008450
-
cfMethyl-seq data (cfSort study) from serial plasma samples of NSCLC patients
Dataset
EGAD00001010881
-
NIPT samples for systematic evaluation of BinDel, a software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Dataset
EGAD00001009512
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Genome-wide cell-free DNA termini in patients with cancer
Study
EGAS00001005738
-
Genome-wide cell-free DNA termini in patients with cancer
Study
EGAS00001005747
-
Non-muscle Invasive Bladder Cancer Molecular Subtypes Predict Differential Response to Intravesical Bacillus Calmette-Guérin
Study
EGAS00001006879
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors
Study
EGAS00000000074
-
Systemic Lupus Erythematosus Serum Stimulation of Human Intestinal Organoids Induces Barrier Leakiness and Changes in Goblet Cell Differentiation
Study
EGAS50000000012
-
Carboxylesterase 1 mediates a distinctive metabolic profile of dendritic cells to attain an inflammatory phenotype
Study
EGAS50000000230
-
A Single Cell Transcriptomic Analysis of Human Neocortical Development
Study
phs001836
-
SLCO1B1 Variants and Methotrexate Clearance
Study
phs000426
-
Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Study
phs002990
-
Common Variation in Candidate Genes in the Diabetes Prevention Program
Study
phs000681
-
Role of Tobacco Smoke in Clear Cell Renal Cell Carcinoma
Study
phs002083
-
NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)
Study
phs000362
-
Liquid Biopsy Versus Tissue Biopsy to Assess Acquired Resistance and Tumor Heterogeneity in Gastrointestinal Cancers
Study
phs001853
-
Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors
Study
phs000846
-
Stand Up To Cancer East Coast Prostate Cancer Research Group
Study
phs000915
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Study
phs000482
-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development
Study
phs003448
-
ILyAD (Indolent Lymphoma And vitamin D)
Study
phs003503
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
NCI Cancer Model Development for the Human Cancer Model Initiative (HCMI)
Study
phs001486
-
Single Cell and Spatial Transcriptomic Profiling of Haemophilus ducreyi Infection
Study
phs003754
-
Multiple Myeloma Clinical Targeted Sequencing of Patient Samples
Study
phs003908
-
PCR-free shallow whole genome sequencing for chromosomal copy number detection from plasma of cancer patients is an efficient alternative to the conventional PCR-based approach
Study
EGAS00001004692
-
Coding and regulatory somatic profiling of triple-negative breast cancer in Sub-Saharan African patients
Study
EGAS50000001013
-
Epigenetic Control of Topoisomerase 1 by MacroH2A1.1
Study
phs003729
-
Genomic Characterization of Duke Melanoma Brain Metastases
Study
phs003009
-
Whole-genome and transcriptome versus panel sequencing in precision oncology: A translational-clinical comparison
Study
EGAS50000000431
-
Singel-cell RNA sequencing and CUT&RUN sequencing of human RUNX2-deficient osteoblasts
Study
JGAS000663
-
Mutational signatures in normal tissues of patients treated with clinical stage G-quadruplex binder CX5461
Study
EGAS50000001145
-
Transcriptome profiling of megakaryocytes and platelets: application to GP9- and IKZF5-related thrombocytopenia
Study
EGAS50000001276
-
Complex genotype-phenotype relationships shape the response to treatment of Down Syndrome Childhood Acute Lymphoblastic Leukaemia
Study
EGAS50000001287
-
Comprehensive genomic analysis of colorectal cancer with microsatellite instability
Study
JGAS000113