-
Genomic Sequencing of Cervical Cancers
Study
phs000600
-
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
-
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
-
NextGen Consortium: GENESiPS Study: Identifying the Gene Networks of Insulin Resistance
Study
phs001139
-
Host Genetic Determinants of the Outcome of Staphylococcus Aureus Bacteremia by Whole Exome Sequencing
Study
phs001505
-
Discovery of Non-ETS Gene Fusions in Human Prostate Cancer using Next Generation RNA Sequencing
Study
phs000310
-
Somatic Mutation Profile by Next Generation Sequencing in HER2+ Breast Cancer
Study
phs000770
-
Rapid Evolution of a Skin Lightening Allele in Southern African KhoeSan
Study
phs001753
-
Experimental and Clinical Studies of Presbycusis
Study
phs003327
-
Early Detection of Malignant and Pre-Malignant Peripheral Nerve Tumors Using Cell-Free DNA Fragmentomics
Study
phs003712
-
Reconstructing oral cavity tumor evolution through brush biopsy
Study
EGAS50000000602
-
Transcriptome sequencing of human colon organoid after co-cultivation with Bifidobacterium longum
Study
JGAS000740
-
Genome-Wide Association Study of the Taste and Hedonic Ratings of the Low-Calorie Sweetener Acesulfame Potassium
Study
phs004031
-
Drug Development against Tumor Microtube Networks in Glioblastoma
Study
EGAS50000000477
-
Bruno et al.: Interferon gamma rebalances immunopathological signatures in Chronic Granulomatous Disease through metabolic rewiring
Study
EGAS00001005463
-
Emergence of oncofetal plasticity is ubiquitous in early colorectal cancers
Study
EGAS50000001532
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
The Genomic Landscape of Childhood and Adolescent Melanoma
Study
EGAS00001000901
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Mapping_gene_environment_interactions_in_macrophages
Study
EGAS00001002268
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data
Study
EGAS00001002728
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-009
Study
EGAS00001004290
-
Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
-
P647_Targeted_resequencing_project
Study
EGAS00001000305
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Molecular determinants of response to PD-L1 blockade across tumor types
Study
EGAS00001004343
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
The_Genomic_Advances_in_Sepsis__GAinS__RNA_seq
Study
EGAS00001003772
-
Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
-
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Study
EGAS00001005053
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-010
Study
EGAS00001004291
-
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Study
EGAS00001005098
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005215
-
CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase
Study
EGAS00001004455
-
Regulatory T cell transcriptomic reprogramming characterizes adverse events by checkpoint inhibitors in solid tumors
Study
EGAS00001004694
-
Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC-- CA209-025
Study
EGAS00001004292