-
BARIA baseline first 100 individuals transcriptomes
Study
EGAS00001005704
-
The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Study
EGAS00001002737
-
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
-
Somatic IL4R Hotspot Mutations in Primary Mediastinal Large B-cell lymphoma lead to constitutive JAK-STAT activation
Study
EGAS00001002796
-
Hominin-specific NOTCH2 paralogs expand human cortical neurogenesis through regulation of Delta/Notch interactions.
Study
EGAS00001002798
-
Clonal evolution in myeloma: the impact of maintenance lenalidomide and depth of response on the genetics and sub-clonal structure of relapsed disease in uniformly treated newly diagnosed patients
Study
EGAS00001003539
-
Reference Exome Data for a Northern Brazilian population
Study
EGAS00001004112
-
SHANK2 mutations associated with Autism Spectrum Disorder cause hyperconnectivity of human neurons
Study
EGAS00001003436
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
scRNA-seq of HSPC treated with gemcitabine and carbplatin
Study
EGAS00001004381
-
Clinical significance of novel subtypes of acute lymphoblastic leukemia in the context of minimal residual disease-directed therapy
Study
EGAS00001005084
-
Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Study
EGAS00001005144
-
UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
-
Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Study
EGAS00001003286
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Identification of rare germline variants in familial multiple myeloma
Study
EGAS00001004734
-
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
-
Risk and modifying factors in Frontotemporal Dementia
Study
EGAS00001004895
-
Epigenome wide DNA methylation assay of gingivo-buccal oral squamous cell carcinoma using single base resolution high throughput array
Study
EGAS00001003896
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670