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Somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated lung adenocarcinoma patients
Dataset
EGAD00001007505
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Genotyping of GM samples
Dataset
EGAD00001010255
-
WGS of off-target analysis of prime editing in organoids
Dataset
EGAD00001007744
-
Whole-genome sequencing of BCR-ABL1 lymphoblastic leukemia
Dataset
EGAD00001010323
-
Sporadic Parathyroid Carcinoma
Dataset
EGAD00001000370
-
Somatic pseudogenes acquired during cancer development – RNAseq
Dataset
EGAD00001000639
-
ICR_RNASeq_pHGG
Dataset
EGAD00001004116
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Dataset
EGAD00001001662
-
Illumina sequencing of V4 variable region of the 16S rRNA from human feces samples
Dataset
EGAD00001004944
-
Role of HPV and Interferon in APOBEC mutational signature (2019-04-11)
Dataset
EGAD00001004955
-
Immunoglobulin sequences of self-reactive plasma cells in celiac disease
Dataset
EGAD00001005029
-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Dataset
EGAD00001005798
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Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation
Study
phs001512
-
Identification and Molecular Characterization of Somatic Mutations in Malformations of Cortical Development
Study
phs002128
-
Pathways Study
Study
phs001534
-
Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)
Study
phs001350
-
Mapping Systemic Lupus Erythematosus Heterogeneity at the Single Cell Level
Study
phs002048
-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
Genome-Wide Analysis for Addiction Susceptibility Genes
Study
phs001266
-
Host Genetic Determinants of the Outcome of Staphylococcus Aureus Bacteremia by Whole Exome Sequencing
Study
phs001505
-
Gabriella Miller Kids First Pediatric Research Program for Infantile Hemangiomas Associated with Multi-Organ Structural Birth Defects
Study
phs001785
-
Comparison Between qPCR and RNA-Seq Reveals Challenges of Quantifying HLA Expression
Study
phs003177
-
Whole Genome Association Study of Visceral Adiposity in the Health Aging and Body Composition (Health ABC) Study
Study
phs000169
-
PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Study
phs003475
-
Gene Expression and Biomarker Utility in Post-Mortem Samples
Study
phs003546
-
DEMENTIA-SEQ: WGS in Lewy Body Dementia and Frontotemporal Dementia
Study
phs001963
-
Integrative Gene Regulatory Network Analysis Discloses Key Driver Genes of Fibromuscular Dysplasia
Study
phs003674
-
Center for Common Disease Genomics [CCDG] Neuropsychiatric: Autism Spectrum Disorder (ASD) – Whole Exomes
Study
phs002502
-
Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Study
EGAS50000000484
-
3D tissue engineered human skeletal muscle modelling Facioscapulohumeral Muscular Dystrophy
Study
EGAS50000000502
-
Childhood Cancer Data Initiative (CCDI): Pediatric In Vivo Testing Program –Sarcoma, Kidney, and Liver Cancers
Study
phs003160
-
Imaging: Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
Study
phs003963
-
Hematopoietic Tet2 inactivation enhances the response to checkpoint blockade immunotherapy
Study
EGAS50000001191
-
Bruno et al.: Interferon gamma rebalances immunopathological signatures in Chronic Granulomatous Disease through metabolic rewiring
Study
EGAS00001005463
-
Comprehensive gene analysis of colorectal cancer cases
Study
JGAS000128
-
Microbiomic and immunogenic biomarkers of adjuvant chemotherapy efficacy in stage III colorectal cancer
Study
JGAS000875
-
Myeloid cell networks govern re-establishment of original immune landscapes in recurrent ovarian cancer
Study
EGAS50000001069
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Study
EGAS00001002211
-
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Study
EGAS00001001386
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
P647_Targeted_resequencing_project
Study
EGAS00001000305
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Study
EGAS00001004327