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The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Study
EGAS00001004434
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Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
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Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840
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H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
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Genome Asia 100K Project
Study
EGAS00001002921
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Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
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Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
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Whole exome sequencing CYLD cutaneous syndrome
Study
EGAS00001003839
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Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
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Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
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Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
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Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Study
EGAS00001004472
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Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Study
EGAS00001003388
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Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Study
EGAS00001004477
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Multimodal single-cell and bulk glioma analyses
Study
EGAS00001005300
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COVID19 Host Genetic Initiative
Study
EGAS00001005304
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Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
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Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
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An epigenomics time course analysis of covid19 patients from Quebec, Canada
Study
EGAS00001005468
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Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892
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Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
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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
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WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
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Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
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Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
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The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
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Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Study
EGAS00001003952
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RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
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Whole genome sequencing for novel neuromuscular disease gene discovery
Study
EGAS00001004535
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Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
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WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
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Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
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Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
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The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
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Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
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Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
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Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
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Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Study
EGAS00001003003
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Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
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Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Study
EGAS00001004014
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Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
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SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
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Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
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Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
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Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005408
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Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889