-
Sanger sequencing of catalytic-domain encoding exons of tyrosine kinase genes from human endometrial tumor DNAs
Study
phs000841
-
The National Heart, Lung, and Blood Institute (NHLBI)-funded Next Generation Genetic Association Studies (NextGen) Consortium: Phenotyping Lipid traits in iPS derived hepatocytes Study (PhLiPS Study)
Study
phs001341
-
Identification and Targeting of Inflammatory Macrophage-Fibroblast Crosstalk in Rheumatoid Arthritis
Study
phs001340
-
NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001468
-
National Eye Institute (NEI) Exfoliation Genotyping Study
Study
phs001053
-
Genetic analysis of Hirschsprung disease
Study
phs000497
-
Creatine in Huntington's Disease (HD) (CREST-E)
Study
phs001488
-
Identification of Targetable FGFR Gene Fusions in Diverse Cancers
Study
phs000602
-
International Multi-Center ADHD Genetics Project
Study
phs000016
-
Autism Post-Mortem Brain RNA-Sequencing: SRRM4 Splicing Study
Study
phs000872
-
Cross-Species Single-Cell Analysis of Pancreatic Ductal Adenocarcinoma Reveals Antigen-Presenting Cancer-Associated Fibroblasts
Study
phs001840
-
Longitudinal Study of Bone and Endocrine Disease in Children with MPS I, II, and VI: A Multicenter Study of the Lysosomal Disease Network
Study
phs001576
-
A Whole Genome Association Search for Type 2 Diabetes Genes in African Americans
Study
phs000140
-
Comparison Between qPCR and RNA-Seq Reveals Challenges of Quantifying HLA Expression
Study
phs003177
-
Identification of Host Genetic Factors That Are Determinant for the Development of Severe Forms of COVID-19
Study
phs003512
-
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
Study
phs002033
-
Integrative Gene Regulatory Network Analysis Discloses Key Driver Genes of Fibromuscular Dysplasia
Study
phs003674
-
Full characterization of structural variation
Study
EGAS50000000520
-
Identifying New Genetic Subtypes in Follicular Lymphoma
Study
EGAS50000000435
-
snRNA: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000786
-
bulk ATACseq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000787
-
scATAC: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000788
-
bulk RNA-seq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000789
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program –Sarcoma, Kidney, and Liver Cancers
Study
phs003160
-
APOBEC3 mutagenesis drives therapy resistance in breast cancer
Study
EGAS50000000875
-
Examination of Engineered LINE-1 Integration Events in HeLa Cells
Study
phs001669
-
Spatial transcriptomics elucidates medulla niche supporting germinal center response in myasthenia gravis thymoma
Study
JGAS000672
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
Microbiomic and immunogenic biomarkers of adjuvant chemotherapy efficacy in stage III colorectal cancer
Study
JGAS000875
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19
Study
EGAS00001005735
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Study
EGAS00001003963
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Study
EGAS00001002406
-
Variation and transmission of the human gut microbiota across generations - shotgun data
Study
EGAS00001005649
-
Variation and transmission of the human gut microbiota across generations - 16S data
Study
EGAS00001005651
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005215
-
T cell responses of ALS patients
Study
EGAS00001006675
-
Longitudinal evaluation of serum microRNAs as biomarkers for neuroblastoma burden and therapeutic p53 reactivation
Study
EGAS00001006678
-
Human leukocyte antigen alleles associate with COVID-19 vaccine immunogenicity and risk of breakthrough infection
Study
EGAS00001006909
-
Targeting TRIP13 in Wilms Tumor with Nuclear Export Inhibitors
Study
EGAS00001007389
-
Integrative Multi-Omics and Drug Sensitivity Profiling Reveals Potential Predictive Biomarkers in Pediatric Solid Tumors from the INFORM Registry
Study
EGAS00001008249
-
Cancer Genome Project Exome Sequencing
Dataset
EGAD00001000289
-
RNA-seq of STIC lesions and adjacent normal samples
Dataset
EGAD50000000289
-
scRNAseq of co-culture of human organoids with polarized pro-inflammatory or anti-inflammatory macrophages
Dataset
EGAD50000000675
-
Single cell RNA sequencing of co-culture of human organoids with polarized pro-inflammatory (M1) or anti-inflammatory (M2) macrophages
Dac
EGAC50000000270
-
Resolution of Ring Chromosomes, Robertsonian Translocations, and Complex Structural Variants from Long-Read Sequencing and Telomere-to-Telomere Assembly
Study
phs003779
-
WGS dataset for Multimodal antigenic escape to GPRC5D-targeted T-cell engagers in multiple myeloma
Dataset
EGAD50000001643
-
Ankara Bilkent City Hospital Clinical Research Ethics Committee
Dac
EGAC50000000940
-
Genome-wide study of resistance to severe malaria in eleven worldwide populations
Study
EGAS00001001311
-
Analysis of resistance to PLX4032 (2019-08-21)
Dataset
EGAD00001005278
-
Pre-clinical evolution of haematological malignancies_TGS
Dataset
EGAD00001006424
-
Transcriptomic response of miRNAs of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Dataset
EGAD00001006181
-
Cancer initiation organoids BAM files
Dataset
EGAD00001002719
-
RNAseq of primary mesothelioma cell lines
Dataset
EGAD00001010924
-
Pre-diagnostic saliva microbiota of Finnish children with autoimmune diseases
Dataset
EGAD00001009984
-
RNAseq of primary mesothelioma cell lines
Dataset
EGAD00001009642
-
Unifying recovery dynamics in heterogeneous diseases exemplified by COVID-19
Dataset
EGAD00001008331
-
To profile the landscape of sebaceous tumours_RNAseq
Dataset
EGAD00001015368
-
Pre-clinical evolution of haematological malignancies_WGS
Dataset
EGAD00001006423
-
Whole Genome sequencing of individuals from Carlantino, Italy
Dataset
EGAD00001000774
-
Exome sequencing data to study therapeutic targeting of ependymoma
Dataset
EGAD00001003973
-
WES analysis of patients with USP8 wild-type corticotroph adenomas
Dataset
EGAD00001004136
-
Chondrosarcoma Validation Study
Dataset
EGAD00001000392
-
A Single Cell Transcriptomic Analysis of Human Neocortical Development
Study
phs001836
-
Somatic Genome Dynamics of Barrett's Esophagus Patients with Non-Cancer and Cancer Outcomes
Study
phs001912
-
Clonally selected lines after CRISPR/Cas editing are not isogenic
Study
phs003110
-
Norepinephrine Transporter Blockade as a Pathophysiological Biomarker in Neurogenic Orthostatic Hypotension
Study
phs001595
-
Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Study
phs001133
-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
NCI Cancer Model Development for the Human Cancer Model Initiative (HCMI)
Study
phs001486
-
Epigenetic Control of Topoisomerase 1 by MacroH2A1.1
Study
phs003729
-
Genomic Characterization of Duke Melanoma Brain Metastases
Study
phs003009
-
Colon Cancer Family Registry (Colon CFR)
Study
phs002733
-
CAGE-seq analysis of osteoblast derived from cleidocranial dysplasia human induced pluripotent stem cells
Study
JGAS000248
-
DNA demethylation is associated with malignant progression of low-grade gliomas
Study
JGAS000146
-
An autoinflammatory RIG-I variant causing Singleton-Merten Syndrome associates with small non-coding Y-RNAs
Study
EGAS50000001660
-
Sequencing and analysis of a South Asian-Indian personal genome
Study
EGAS00001000328
-
Targeted and shallow whole genome sequencing identifies therapeutic opportunities in p53abn endometrial cancers
Study
EGAS00001007661
-
Benchmarking for alignment and variant calling
Study
EGAS00001007819
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
Characterization of a human iPSC-derived islet differentiation model
Study
EGAS00001002721
-
TRACERx 100: whole exome data of the first 100 TRACERx tumours
Study
EGAS00001002247
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
Transcriptome_human_nasal_epithelium
Study
EGAS00001001294
-
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
-
Exome sequencing
Study
EGAS00001005761
-
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Study
EGAS00001004753
-
Non-viral precision T cell receptor replacement for personalized cell therapy
Study
EGAS00001006898
-
scRNAseq for patients with immunodeficiency and HCs
Study
EGAS00001007271
-
Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency
Study
EGAS00001007393
-
The genotype of LAM disease
Dataset
EGAD00010001689
-
Molecular Profiling of Gallbladder Cancer (MPOG)
Study
phs001404