-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
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
-
Genomic landscape and PD-1 blockade in Natural-killer/T cell lymphoma
Study
EGAS00001003828
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
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
-
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
-
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
-
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Study
EGAS00001004434
-
H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
-
Genome Asia 100K Project
Study
EGAS00001002921
-
Whole exome sequencing CYLD cutaneous syndrome
Study
EGAS00001003839
-
Targeted sequencing CYLD cutaneous syndrome
Study
EGAS00001003840
-
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
-
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
-
The genomic landscape of lung adenocarcinoma in East Asians
Study
EGAS00001002941
-
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
-
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
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
-
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
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
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
-
Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
-
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003137
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003139
-
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Study
EGAS00001003870
-
Systematic comparative analysis of single-nucleotide variants detection methods from single-cell RNA sequencing data
Study
EGAS00001003883
-
Whole-exome sequencing of the transposition of the great arteries
Study
EGAS00001004175
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Study
EGAS00001004316
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Study
EGAS00001003184
-
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
-
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort
Study
EGAS00001002499
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
Hepatoblastoma tumoroid biobank as a key resource for tumour genetics
Study
EGAS00001008251
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
-
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Study
EGAS00001004359
-
Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067)
Study
EGAS00001004363
-
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207
-
Multiple Sclerosis Replication Chip data (MS Chip)
Study
EGAS00001003216
-
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
-
Genomic landscape of oral cancers (Illumina WGS)
Study
EGAS00001003228
-
An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy
Study
EGAS00001003234
-
Personalised Mapping of Tumour Development in Synchronous Colorectal Cancer Patients
Study
EGAS00001004413
-
A mechanistic classification of clinical phenotypes in neuroblastoma
Study
EGAS00001003244
-
46 CLL Whole Genome Sequencing Study
Study
EGAS00001003254
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Study
EGAS00001004478
-
Fine-Scale Genomic Analyses Of Admixed Individuals Reveal Unrecognized Genetic Ancestry Components In Argentina
Study
EGAS00001004492
-
An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition
Study
EGAS00001004523
-
Novel mutations in TOP2A in gliomas
Study
EGAS00001004556
-
The endometrial transcription landscape of MRKH syndrome
Study
EGAS00001004601
-
Patient-tailored design for selective co-inhibition of leukemic cell subpopulations
Study
EGAS00001004614
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Study
EGAS00001004663
-
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Study
EGAS00001004682
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Study
EGAS00001004705