-
Integrated single-cell profiling dissects cell-state-specific enhancer landscapes of human tumor infiltrating T cells.
Study
EGAS00001006141
-
Enhancer profiling to identify identifies epigenetic markers of endocrine resistance in metastatic castration resistant prostate cancer patients
Study
EGAS00001006161
-
Transcriptomic and epigentic analysis of human peripheral blood NK cell subsets revealing role of Bcl11b in differentiation
Study
EGAS00001005025
-
Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001002742
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
Genetic Determinants of Mannose-binding Lectin Activity Predispose to Thromboembolic Complications in Critical COVID-19
Study
EGAS00001006266
-
Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Study
EGAS00001004117
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Indonesian RNA-seq data
Study
EGAS00001003671
-
Evolutionary predictability of genetic versus non genetic resistance to anticancer drugs in melanoma
Study
EGAS00001005314
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
-
Case Report: early contribution of germline and nevi genetic alterations to a rapidly-progressing Cutaneous Melanoma Patient
Study
EGAS00001006459
-
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Study
EGAS00001003828
-
Whole genome and whole exome sequencing of epilaptic patients
Study
EGAS00001002825
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
-
Neuroblastoma tumor heterogeneity and cell plasticity (from patients)
Study
EGAS00001005322
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
-
Egyptref: An integrated personal and population-based Egyptian genome reference
Study
EGAS00001004303
-
VIKING Health Study - Shetland
Study
EGAS00001003872
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
HLF COPD DNA Methylomics
Study
EGAS00001006603
-
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
-
Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
-
EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION
Study
EGAS00001001645
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
Comprehensive Whole-Genome Sequence Annotation to Resolve the Genetic Architecture of Cerebral Palsy
Study
EGAS00001006724
-
Profiling_heterogeneity_in_Human_derived_IPSC_neurons
Study
EGAS00001002885
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
Exome sequencing demonstrates a dual origin of relapses in retinoic-acid resistant acute promyelocytic leukemia.
Study
EGAS00001002893
-
Highly sensitive liquid biopsy Duplex sequencing complements tissue biopsy to enhance detection of clinically relevant genetic variants
Study
EGAS00001006805
-
Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
-
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
-
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Study
EGAS00001004434
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
-
H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
-
Genetic landscape of ENKTCL
Study
EGAS00001006906
-
Genome Asia 100K Project
Study
EGAS00001002921
-
Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
-
Identifying rare genetic variants in 21 highly multiplex autism families
Study
EGAS00001006928
-
Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
-
Whole exome sequencing CYLD cutaneous syndrome
Study
EGAS00001003839
-
Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840
-
Longitudinal peripheral blood DNA methylation profiling of endoscopic response to tofacitinib in moderate-to-severe ulcerative colitis patients
Study
EGAS00001006968
-
Therapeutic vulnerabilities in CCA from different etiologies identified using integrative multi-omics enhancer activity profiling
Study
EGAS00001007309
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Study
EGAS00001004472
-
Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Study
EGAS00001003388
-
Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Study
EGAS00001004477
-
Multimodal single-cell and bulk glioma analyses
Study
EGAS00001005300
-
The genomic landscape of lung adenocarcinoma in East Asians
Study
EGAS00001002941
-
COVID19 Host Genetic Initiative
Study
EGAS00001005304
-
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
An epigenomics time course analysis of covid19 patients from Quebec, Canada
Study
EGAS00001005468
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
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
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
Elevated cfDNA after exercise is derived primarily from mature polymorphonuclear neutrophils, with a minor contribution of cardiomyocytes
Study
EGAS00001007157
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
HELIUS cohort
Study
EGAS00001002969
-
Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Study
EGAS00001003952
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
-
Whole genome sequencing for novel neuromuscular disease gene discovery
Study
EGAS00001004535
-
Integrated genetic analysis of primary CNS lymphoma
Study
EGAS00001007222
-
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
-
Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
-
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Study
EGAS00001007560
-
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
-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
-
Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
-
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
-
Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Study
EGAS00001004014
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
Methylome study on human spermatogenic cells
Study
EGAS00001007449
-
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
-
Expression-Based Subtypes Define Pathologic Response to Neoadjuvant Immune-Checkpoint Inhibitors in Muscle-Invasive Bladder Cancer
Study
EGAS00001005549