-
Genomic characterization of hepatocellular carcinoma in Hispanic patients
Study
EGAS00001007431
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
Targeted deep sequencing on Pediatric MDS
Study
EGAS00001005431
-
The transcriptomic response of skeletal muscle in life-long high-level trained and untrained men and women after acute exercise
Study
EGAS00001006139
-
Clonal dominance defines metastatic dissemination in pancreatic cancer
Study
EGAS00001006358
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
A PROSTATE TUMORGRAFT PANEL TO ACCELERATE PRECISION MEDICINE
Study
EGAS00001007033
-
RNA sequencing on intestinal biopsies from inflammatory bowel disease patients treated with vehicle control, MEK inhibitor, or infliximab
Study
EGAS00001007534
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Exome trios in patients with gastroschisis (2019-04-08)
Dataset
EGAD00001004942
-
Small-molecule inhibitors in melanoma - Kenski / Kong - WES (2019-04-11)
Dataset
EGAD00001004952
-
RNA sequencing of periprostatic fat after a 6 month deep androgen deprivation therapy
Dataset
EGAD00001004971
-
Somatic mutation and clonal evolution normal breast tissue TGS (2020-01-15)
Dataset
EGAD00001005787
-
Molecular profiling of tissue autopsies and ctDNA
Dataset
EGAD00001007040
-
Molecular characterization of NASH-HCC
Dataset
EGAD00001007524
-
Somatic mutation rates scale with lifespan across mammals
Dataset
EGAD00001008032
-
Whole-genome sequencing of high-grade serous ovarian cancer (HGSC) tumours and matched normals from long-term survivors.
Dataset
EGAD00001009398
-
Organoid Derivation Project: WGS (2023-06-22)
Dataset
EGAD00001011090
-
Genome and transcriptome sequence data from a pre-B all (2nd relapse in CNS) tumor patient
Dataset
EGAD00001015291
-
Genome and transcriptome sequence data from a diffuse aarge B-cell lymphoma (relapse) tumor patient
Dataset
EGAD00001015308
-
Genome and transcriptome sequence data from a relapsed blastic plasmacytoid dendritic cell neoplasm tumor patient
Dataset
EGAD00001015312
-
Insights into non-crossover recombination from long-read sperm sequencing
Dataset
EGAD00001015736
-
On-target mutations confer resistance to WRN helicase inhibitors in Microsatellite Unstable Cancer Cells
Dataset
EGAD00001015822
-
Fecal microbiome subtype affects the clinical and genomic aberrations of colorectal cancer
Study
JGAS000696
-
Combined – whole blood and skin fibroblasts - transcriptomic analysis in Psoriatic arthritis.
Study
EGAS00001006288
-
Neoantigen-Targeted CD8+ T-Cell Responses 1 With PD-1 Blockade Therapy
Study
phs003153
-
Prevention and Early Treatment of Acute Lung Injury Network - Vitamin D to Improve Outcomes by Leveraging Early Treatment (PETAL VIOLET-BioLINCC)
Study
phs003879
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) Acetaminophen in Sepsis: Targeted Therapy to Enhance Recovery (ASTER) (PETAL ASTER-BioLINCC)
Study
phs003900
-
Cryptococcosis in Previously Healthy Adults
Study
phs003871
-
PE-CGS: Optimizing Engagement of Hispanic Colorectal Cancer Patients in Cancer Genomic Characterization Studies
Study
phs003985
-
Patient Registry for Primary Pulmonary Hypertension (PPH Registry-BioLINCC)
Study
phs004275
-
Whole transcriptome RNA sequencing as comprehensive diagnostic tool for acute myeloid leukemia.
Study
EGAS00001003096
-
Beyond BRCA deficiency: Clinical and molecular predictors of survival in patients with BRCA-deficient tubo-ovarian high-grade serous carcinoma
Study
EGAS00001008059
-
Genetic Causes of Growth Disorders
Study
phs001617
-
Multiple Myeloma Genomic Study (MMGS)
Study
phs001323
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
Accelerating Medicines Partnership-Systemic Lupus Erythematosus (AMP-RA/SLE)
Study
phs001459
-
Single Cell Analysis of Pulmonary Fibrosis
Study
phs001750
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Targeted Sequencing of Primary ER-positive Breast Tumors Treated with 5 Years of Tamoxifen
Study
phs001234
-
The Longevity Genes Project
Study
phs000584
-
HNPCC-Sys: Molecular Characterization of Lynch Syndromes
Study
phs001407
-
HuBMAP: Single-Cell Data from Human Tissues
Study
phs002272
-
Time Lapse to Cancer-Defining the Transition from Polyp to Cancer
Study
phs001384
-
Melanoma Brain Metastasis Single-Cell RNA Sequencing Atlas
Study
phs002944
-
Evolution of Resistance in ER+ Breast Cancer
Study
phs002287
-
Transcriptomic and Clonal Characterization of T Cells in the Human Central Nervous System
Study
phs002222
-
DNA Methylation Analysis of Peripheral Blood Cells from Siblings Discordant for ASD
Study
phs000619
-
Multimodal Mapping of the Immune Landscape in Human Pancreatic Cancer
Study
phs002071
-
Accelerating Medicines Partnership-Rheumatoid Arthritis (AMP-RA/SLE)
Study
phs001457
-
AACR Project Genomics, Evidence, Neoplasia, Information, Exchange (GENIE)
Study
phs001337
-
TCGA WGS Variants Across 18 Cancer Types
Study
phs003155
-
Development and Validation of Organoids from Fibrolamellar Carcinoma Human Cells
Study
phs002439
-
Somatic Mutations in Epilepsy: Whole Genome Sequence Analysis of Single Neurons
Study
phs002615
-
Dysregulation of Naive T Cell Quiescence during Aging
Study
phs003400
-
Clinical Outcomes and ctDNA Correlates for CAPOX BETR: A phase II trial of Capecitabine, Oxaliplatin, Bevacizumab, Trastuzumab in Previously Untreated Advanced HER2+ Gastroesophageal Adenocarcinoma
Study
phs003706
-
Developing Targeted Therapy for Patients with Multiple Myeloma and Gain or Amplification of Chr1q (1q+)
Study
phs003886
-
Construction of Thousands of Single Cell Genome Sequencing Libraries Using Combinatorial Indexing
Study
phs001268
-
Whole genome sequencing of human induced pluripotent stem cells derived from 5 type I cyctic biliary atresia patients
Study
JGAS000765
-
exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers
Study
JGAS000488
-
The characterization of gene expression pattern of anticancer agent-resistant cancer stem cells using RNA sequencing analysis.
Study
JGAS000350
-
High-coverage whole exome sequence in non-TRU-type lung adenocarcinomas
Study
JGAS000105
-
Development of humanized mice for human hematopoisis and immunity research
Study
JGAS000122
-
Truncated FOS impairs osteogenic differentiation and induces prostaglandin and NFkB signalling in an in vitro cell-of-origin model for osteoid osteoma and osteoblastoma
Study
EGAS50000001291
-
Germline Aberrations of PAX5 Cause Susceptibility to pre-B cell Acute Lymphoblastic Leukemia
Study
EGAS00001000447
-
An allele-resolved nanopore-guided tour of the human placental methylome
Study
EGAS50000001301
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Study
EGAS50000001327
-
Head and neck tumor organoid biobank for modelling individual responses to radiation therapy according to the TP53/ HPV status
Study
EGAS50000001219
-
Recording physiological history of cells with chemical labeling.
Study
EGAS50000000056
-
Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes
Study
EGAS50000000279
-
A single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas
Study
EGAS50000000342
-
Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib
Study
EGAS50000000372
-
10x genomics single cell RNA-seq and ATAC-seq from 10 pre-menopausal patients fimbriae and ampullary part of the fallopian tube
Study
EGAS50000000628
-
Single cell multi-omics analysis of chromothriptic medulloblastoma highlights genomic and transcriptomic consequences of genome instability
Study
EGAS00001005410
-
Clinical relevance of TCGA subtypes for gastric cancer patients
Study
EGAS50000000779
-
Nala TAS-LRS PGx Study
Dataset
EGAD50000001609
-
Identification of the underlying causal variant in a multi-generational family with autosomal dominant common variable immunodeficiency
Dataset
EGAD00001000363
-
RNA-Seq of human longitudinal whole blood samples from PCR-positive and PCR-negative recent household contacts of COVID-19 index cases.
Study
EGAS50000000473
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Size-tagged preferred ends in maternal plasma DNAshed light on the production mechanism and showutility in noninvasive prenatal testing
Study
EGAS00001002831
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
Genetic landscape of malignant peripheral nerve sheath tumors
Study
EGAS00001000974
-
Exome sequence data for germline, primary tumor, and relapse tumor of a transformed non-Hodgkins lymphoma patient with unexpected long-time remission
Study
EGAS00001001973
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
Whole exome sequencing in RVOT patients
Study
EGAS00001002319
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
Recurrent Somatic Mutations of PTPN1 in Primary Mediastinal B cell lymphoma and Hodgkin Lymphoma
Study
EGAS00001000554
-
ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
-
Cross-species genomics identifies TAF12, NFYC and RAD54L as novel choroid plexus carcinoma oncogenes
Study
EGAS00001000961
-
Two lung cancer cell lines with EGFR mutations, PC-9 and KHM-3S, were either treated with Tarceva for 24 hours or left untreated. The gene expression profiles were examined by RNAseq, and the genome wide binding profiles of total STAT3 and pSTAT3 were characterized by ChIPseq.
Study
EGAS00001000793
-
Spatio-temporal evolution of the primary glioblastoma genome
Study
EGAS00001001041
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition
Study
EGAS00001002115
-
Multisample genomic analysis of solid childhood cancers using high resolution SNP-arrays, Whole Exome Sequencing and Targeted Deep Sequencing.
Study
EGAS00001002662
-
An Unusual Genomic Variant of Pancreatic Ductal Adenocarcinoma with an Indolent Clinical Course
Study
EGAS00001002192
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
Circulating cell-free DNA analysis in Small Cell Lung Cancer
Study
EGAS00001003110