-
Genome and transcriptome sequence data from a metastatic rectal carcinoma patient
Dataset
EGAD00001004936
-
Field effect of healthy and diseased livers (2019-04-08)
Dataset
EGAD00001004941
-
CyTOF of 27 DLBCLs
Dataset
EGAD00001005419
-
Understanding Self- Organising Capacity of Stem Cells during Implantation and Early Post-implantation Development in vitro and in vivo: Implications for Human Development (2020-04-20)
Dataset
EGAD00001006056
-
Genomic characterisation of MGUS
Dataset
EGAD00001006363
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Dataset
EGAD00001006894
-
Single-cell study of 14 childhood medulloblastoma patients
Dataset
EGAD00001009057
-
Renal habitat WXS
Dataset
EGAD00001010125
-
Insertion Site Analysis of T cells in a CD19-CAR Study on the T-SCM effect in B-cell malignancies
Dataset
EGAD00001015540
-
Single-cell level characterization of B cell depletion and repopulation following rituximab in systemic lupus erythematosus
Dataset
EGAD00001015817
-
The Haplotype Reference Consortium
Study
EGAS00001001710
-
Sequential single-cell transcriptional and protein marker profiling reveals TIGIT as a marker of CD19 CAR-T cell dysfunction in patients with non-Hodgkin’s lymphoma
Study
EGAS00001005356
-
Transcriptome analysis of endometrial organoids derived from patients with Mayer-Rokitansky-Küster-Hauser syndrome
Study
EGAS00001005908
-
Idiopathic Pulmonary Fibrosis Network AntiCoagulant Effectiveness in Idiopathic Pulmonary Fibrosis (IPFNet-ACE-IPF-BioLINCC)
Study
phs004070
-
Gene Expression Study of Individuals with Sex Chromosome Aneuploidies
Study
phs002481
-
A Phase II Neoadjuvant Study of Palbociclib in Combination with Letrozole and Trastuzumab as Neoadjuvant Treatment of Stage II-III ER+ HER2+ Breast Cancer (PALTAN)
Study
phs003147
-
Genetic Markers of Lipids in Indians: A Validation Study of Most Relevant Findings of Genome-Wide Association Studies
Study
phs003469
-
TARGET Trial Study Cohort
Study
phs003720
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Study
EGAS00001004196
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Pharmacokinetic Polymorphisms in Japanese General Population
Study
phs002985
-
Successful Clinical Response in Pneumonia Therapy (SCRIPT)
Study
phs002300
-
Assessment of RNA-Seq Sample Preparation Methodology
Study
phs003001
-
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
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - OncoArray Genotypes
Study
phs001265
-
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
-
Center for Oral Health Research in Appalachia (COHRA) Genomic Studies of Oral Health and Disease
Study
phs001591
-
Single-Cell Mitochondrial Mutation Lineage Tracing of Non-Dysplastic and Dysplastic Barrett's Esophagus
Study
phs003949
-
Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): CO-CREATE-Ex: Community-engaged Optimization of COVID-19 Rapid Evaluation And TEsting Experiences
Study
phs003686
-
TNBC ctDNA Targeted Panel
Study
EGAS00001006937
-
Immunogenomics of Malignant Brain Tumors
Study
phs002612
-
Metformin for Oral Cancer Prevention
Study
phs002437
-
Autosomal recessive CD70 deficiency is associated with combined immunodeficiency and EBV viremia
Study
phs001245
-
Gene-Environment Interactions in COCCaINE Use Disorder: Collaborative Case-Control Initiative in Cocaine Addiction
Study
phs001810
-
International Consortium for Blood Pressure (ICBP)
Study
phs000585
-
The Genomic Analysis of Medulloblastoma
Study
phs000409
-
A Dormant TIL Phenotype Defines Non-Small Cell Lung Carcinomas Sensitive to Immune Checkpoint Blockers
Study
phs001618
-
Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening
Study
phs001482
-
Development and Validation of Patient-Derived Xenografts from Fibrolamellar Carcinoma Human Tissue
Study
phs002435
-
Division of Cancer Epidemiology and Genetics (DCEG) Imputation Reference Dataset
Study
phs000396
-
Preclinical Modeling of Leiomyosarcoma Identifies Susceptibility to Transcriptional CDK Inhibitors through Antagonism of E2F-Driven Oncogenic Gene Expression
Study
phs002587
-
Molecular Genetics of Heroin Dependence in China
Study
phs001213
-
Genomic Characterization of Pediatric Low-Grade Gliomas
Study
phs001054
-
Genetics of Lymphatic Anomalies from Center of Applied Genomics (CAG) at CHOP
Study
phs001802
-
The Epigenomic Atlas of Early Human Craniofacial Development
Study
phs002008
-
Sweden-Schizophrenia Population-Based Case-Control Exome Sequencing
Study
phs000473
-
Genomic landscape of Neutrophilic Leukemias of Ambiguous Diagnosis
Study
phs001799
-
Neutralizing Antibodies against West Nile Virus Identified Directly from Human B Cells by Single-Cell Analysis and Next Generation Sequencing
Study
phs001200
-
Phylogenetic Analyses of Melanoma Reveal Complex Patterns of Metastatic Dissemination
Study
phs000941
-
Single Cell Analysis of Psoriasis Resolution following IL-23 Blockade
Study
phs003351
-
Whole Exome and RNA Sequencing of 22 Patient-Derived Xenografts from Estrogen Receptor-Positive Breast Cancers
Study
phs003324
-
Genomics of Acute Myeloid Leukemia
Study
phs000159
-
Cancer-Restricted Cryptic Antigens Are Targets for T Cell Recognition
Study
phs003887
-
Precision Diagnosis of Neurodevelopmental Disorders in Middle Eastern Populations
Study
phs003917
-
Transcriptomics of PPD and Control LCLs Exposed to Steroid Hormones
Study
phs003820
-
Proteomic measurements in BioBank Japan
Study
JGAS000785
-
Deciphering molecular mechanisms underlying hematological malignancies and development of novel therapeutic approaches
Study
JGAS000603
-
Comparison of WGBS, EPIC array, EM-seq, and Nanopore sequencing in assessing DNA methylation marks
Study
EGAS00001008014
-
CAGE analysis for non-small cell lung carcinoma
Study
JGAS000070
-
Whole genome sequencing and mutation rate analysis of Vietnamese trios with paternal dioxin exposure
Study
JGAS000137
-
Biobank Japan genotype data
Study
JGAS000412
-
Biobank Japan genotype data
Study
JGAS000541
-
Long-read whole genome sequencing of gastric cancer
Study
EGAS50000001607
-
Human periportal liver assembloids recapitulate periportal liver tissue in vitro
Study
EGAS50000000994
-
Re-evaluation of human mitochondrial DNA methylation reveals signals consistent with technical artifacts
Study
EGAS50000001186
-
Identification of putative multiple myeloma (MM) susceptibility genes
Study
EGAS50000001259
-
Transcriptomic profiling of granulosa cells from IVF patients at different ages
Study
EGAS50000000824
-
Next-generation molecular analysis of surgical margins in oral squamous cell carcinoma for assessment of microscopic residual disease and personalized postoperative treatment decision
Study
EGAS50000000823
-
Impact of cryopreservation on transcriptome analysis of peripheral blood mononuclear cells
Study
EGAS50000001196
-
Proteomic Characterization of Intrahepatic Cholangiocarcinoma Identifies Risk-Stratifying Subgroups, Proteins Associated with Time-To-Recurrence, and mTOR Effector Molecule EIF4A1 as a Druggable Therapeutic Target
Study
EGAS50000001343
-
HTAS of CD34+ HSPCs in relation to evaluating gene editing outcomes for CGD-causing variants in CYBA and CYBB
Study
EGAS50000001155
-
10X whole single cell RNA-seq from pre-frontal cortex biopsy
Study
EGAS50000001058
-
Genomic and transcriptomic analysis of thymic epithelial tumors
Study
EGAS00001004227
-
Whole genome sequencing data of paediatric patients with BCR::ABL1 acute lymphoblastic leukemia
Study
EGAS50000001512
-
MPNST - WGS FASTQ
Study
EGAS50000001786
-
MPNST - LCM WGS FASTQ
Study
EGAS50000001789
-
RNA-Sequencing of cervical cancers
Study
EGAS50000000087
-
Transcriptomic profiles of early and late passage metastatic colorectal cancer (mCRC) tumoroids
Study
EGAS50000000108
-
DNA Replication Speed controls Epigenome Integrity and T Cell Fate
Study
EGAS50000001273
-
A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy
Study
EGAS50000000228
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Study
EGAS50000000283
-
Multi-omic analysis of SDHB-related PCPG
Study
EGAS50000000346
-
Metagenomic characterization of tracheal aspirates from non-pulmonary sepsis patients
Study
EGAS50000000384
-
A Genomics-Driven Artificial Intelligence-Based Model Classifies Breast Invasive Lobular Carcinoma and Discovers CDH1 Inactivating Mechanisms
Study
EGAS50000000485
-
Single cell RNAseq 7 days - Calprotectin in vitro effects on human early hematopoiesis
Study
EGAS50000000455
-
Bulk ATACseq 7days - Calprotectin in vitro effects on human early hematopoiesis
Study
EGAS50000000456
-
HIPSD&R-seq enables scalable genomic copy number and transcriptome profiling
Study
EGAS50000000691
-
comparing the snRNA-seq from placentas of mothers with or without obesity
Study
EGAS50000000834
-
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
Study
EGAS00001000287
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
Whole-genome-Sequencing of adult medulloblastoma
Study
EGAS00001000393
-
A Combined Omics and Tissue Biobank for Paediatric Cancers
Study
EGAS50000000209
-
A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Dataset
EGAD50000001712
-
PAX4 loss of function increases diabetes risk by altering human pancreatic endocrine cell development
Dataset
EGAD50000000516
-
Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Study
EGAS00001003705
-
Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001002598
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
ProjectMinE :llumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001003383