-
Comparison of WGBS, EPIC array, EM-seq, and Nanopore sequencing in assessing DNA methylation marks
Study
EGAS00001008014
-
Emirati T2T Assembly
Study
EGAS50000001235
-
A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Dataset
EGAD50000001156
-
Lessons learned from the exome sequencing of nine cases of infertility and the way forward
Study
EGAS50000001320
-
DNA Replication Speed controls Epigenome Integrity and T Cell Fate
Study
EGAS50000001273
-
Integrated Single-Nucleus and Spatial Transcriptomics Elucidate Heterogeneity and Hypoxia-Driven Organization of Supratentorial Ependymoma
Study
EGAS50000001318
-
Whole blood RNAseq from a large ALS case-control study at Univ of Michigan
Study
EGAS50000001019
-
Insights into BRCA1 and TP53 associated breast cancer development from integrated whole genome analysis of mouse model mammary tumors
Study
EGAS50000001402
-
10X whole single cell RNA-seq from pre-frontal cortex biopsy
Study
EGAS50000001058
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Study
EGAS50000000283
-
Splicing signature analysis of RNU2-2 samples
Study
EGAS50000001410
-
Fragmentomics analyses of urinary cell-free DNA permit multi-urologic cancer detection and reduction in tissue biopsies for prostate cancer
Study
EGAS50000001431
-
Identification of putative multiple myeloma (MM) susceptibility genes
Study
EGAS50000001259
-
bulk RNAseq analysis of tumor from 3 non-muscle-invasive bladder cancer patients
Study
EGAS50000001383
-
Transcriptomic profiling of proximal and distal regions of human long head biceps tendon
Study
EGAS50000001454
-
University of Zurich (UZH) - Snedeker lab
Dac
EGAC50000000817
-
Whole genome sequencing data of paediatric patients with BCR::ABL1 acute lymphoblastic leukemia
Study
EGAS50000001512
-
A human induced pluripotent stem cell toolbox for studying sex chromosome effects -transcriptional landscape
Study
EGAS50000000931
-
HTAS of CD34+ HSPCs in relation to evaluating gene editing outcomes for CGD-causing variants in CYBA and CYBB
Study
EGAS50000001155
-
A Single-Cell and Spatial Atlas of Early Human Olfactory Development
Dataset
EGAD50000001712
-
Long-read whole genome sequencing of gastric cancer
Study
EGAS50000001607
-
Human periportal liver assembloids recapitulate periportal liver tissue in vitro
Study
EGAS50000000994
-
Genome-wide evaluation of the maturation of the immune response to the tuberculin skin test from day 2 to day 7
Study
EGAS50000000822
-
Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
Study
EGAS00001000287
-
Genetic landscape of non-Down syndrome acute megkaryoblastic leukemia
Study
EGAS00001000379
-
Whole-genome-Sequencing of adult medulloblastoma
Study
EGAS00001000393
-
Proteomic Characterization of Intrahepatic Cholangiocarcinoma Identifies Risk-Stratifying Subgroups, Proteins Associated with Time-To-Recurrence, and mTOR Effector Molecule EIF4A1 as a Druggable Therapeutic Target
Study
EGAS50000001343
-
Genomic and transcriptomic analysis of thymic epithelial tumors
Study
EGAS00001004227
-
20 years after the first human genome release. Where are we heading?
Blog
20-years-after-the-first-human-genome-release
-
Host-microbe interactions in a novel SARS-CoV-2 human challenge model
Study
EGAS50000001440
-
Identification_of_genes_involved_in_congenital_disorders_of_glycosylation_and_3_methylglutaconic_aciduria
Study
EGAS00001002064
-
Lebanon_HighCov_seq
Study
EGAS00001002085
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Multi-layered molecular characterization defines prognostic subtypes of lung adenocarcinoma in Asian never-smokers
Study
EGAS00001003705
-
Macrophage response in preterm infants compared to term infants
Study
EGAS00001004974
-
Intra-prostatic tumour evolution, steps in metastatic spread and histogenomic associations revealed by integration of multi-region whole genome sequencing with histopathological features
Study
EGAS00001007438
-
hereditary BrEAst Case CONtrol study
Study
EGAS00001005043
-
Illumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001002598
-
Genetic landscape of pediatric Medulloblastoma
Study
EGAS00001000347
-
DNA_repair_in_BLM_deficient_hiPSCs
Study
EGAS00001000740
-
ICGC Oesophageal adenocarcinoma - pilot samples
Study
EGAS00001000559
-
ESGI_Identification_of_novel_genes_and_mechanisms_leading_to_Primary_Ciliary_Dyskinesia
Study
EGAS00001000523
-
ProjectMinE :llumina HiSeqX and HiSeq 2000 whole genome sequence data on 3,001 ALS samples including 212 with known C9orf72 repeat expansions
Study
EGAS00001003383
-
Identification_of_drug_resistance_genes_in_melanoma
Study
EGAS00001000617
-
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Study
EGAS00001000659
-
UQCCR/QCMG brain metastasis sequence analysis
Study
EGAS00001000722
-
Ashkenazi Jewish Leukoencephalopathy
Study
EGAS00001001767
-
Single-cell RNA-sequencing of CD34+ bone marrow cells from patients with SLE, healthy individuals and umbilical cord blood samples
Study
EGAS00001007317
-
Genomic Analysis of Primary Plasma Cell Leukemia reveals Complex Structural Alterations and High Risk Mutational Patterns
Study
EGAS00001003834
-
BLUEPRINT Gene expression analysis during human B-cell differentiation using the Affymetrix Human Genome U219 Array
Study
EGAS00001001197
-
CRC Promoter capture Hi-C
Study
EGAS00001001946
-
Comprehensive analysis of the (epi)genome of pediatric atypical teratoid/rhabdoid tumours (AT/RTs)
Study
EGAS00001001297
-
ICGC Oesophageal adenocarcinoma - Barrett's samples
Study
EGAS00001000726
-
Genomic profiling of IBC
Study
EGAS00001007520
-
Multiregion Whole Exome sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001001436
-
Genome-to-genome analysis highlights the impact of the human innate and adaptive immune systems on the hepatitis C virus
Study
EGAS00001002324
-
Exome sequencing to identify predisposition to Wilms tumour
Study
EGAS00001000904
-
Identifying causative mutations for Thrombocytopenia with Absent Radii
Study
EGAS00001000054
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
-
Samples from the Greek island of Crete, MANOLIS cohort
Study
EGAS00001000067
-
The European Bank for Induced Pluripotent stem cells (EBiSC) is designed to address the increasing demand by iPSC researchers for quality-controlled, disease-relevant research grade iPSC lines, data and cell services.In this study Whole Genome Sequencing was performed on a selection of lines from the project.
Study
EGAS00001002755
-
BRAF_and_MEK_resistant_cell_line_clones
Study
EGAS00001000172
-
Genomic profiling of ovarian adult type granulosa cell tumors
Study
EGAS00001002833
-
Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002938
-
Gastric_Mutational_Signatures__GMS_
Study
EGAS00001002939
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Study
EGAS00001003053
-
Somatic point mutation data from microsatellite unstable colorectal cancers
Study
EGAS00001003101
-
Neoadjuvant chemotherapy alters the genomic landscape and immune microenvironment of breast cancers
Study
EGAS00001003354
-
TRACERx 100: RRBS data from a subset of the first 100 TRACERx tumours
Study
EGAS00001003484
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874
-
Whole genome sequencing of 25 South African individuals with myasthenia gravis
Study
EGAS00001003462
-
Autoimmunity_and_immunodeficiency_COVID19
Study
EGAS00001004489
-
Alveolar Rhabdomyosarcoma case report
Study
EGAS00001004828
-
ABIS_1_MeDIP-seq
Study
EGAS00001001099
-
Whole_exome_sequencing_for_clarification_of_rare_causes_of_axonal_Charcot_Marie_Tooth_disease_
Study
EGAS00001002067
-
MYOSEQ project
Study
EGAS00001002069
-
Lebanon_LowCov_seq
Study
EGAS00001002084
-
HDAC inhibitors in synovial sarcoma cells
Study
EGAS00001002637
-
Illumina Omni5 SNP chip genotyping of MacTel cases and unaffected controls for a genome-wide association study
Study
EGAS00001002249
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
-
EPIC arrays data for chemotherapy response project
Study
EGAS00001004515
-
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysm in humans
Study
EGAS00001005518
-
Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
Study
EGAS00001001923
-
Single-cell RNA-seq data of the tumor microenvironment of lymphocyte-rich Hodgkin lymphoma and other Hodgkin lymphoma subtypes
Study
EGAS00001005541
-
Origins and timing of emerging lesions in advanced renal cell carcinoma
Study
EGAS00001005897
-
Using human induced pluripotent stem cell-derived oligodendrocytes to explore cellular phenotypes associated with t(1;11) translocation.
Study
EGAS00001004595
-
RNA sequencing of undifferentiated sarcomas
Study
EGAS00001003291
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___visium
Study
EGAS00001006045
-
Mutational landscape of eccrine porocarcinoma (sweat gland tumour)
Study
EGAS00001004632
-
Case Report: Precision medicine target revealed by in-vitro modelling of relapsed, refractory ALL from a child with neurofibromatosis
Study
EGAS00001006187
-
Epiclomal: probabilistic clustering of sparse single-cell DNA methylation data
Study
EGAS00001003504
-
Tumor microenvironment study of ovarian granulosa cell tumors
Study
EGAS00001006478
-
Reliable assessment of telomere maintenance mechanisms in neuroblastoma
Study
EGAS00001006510
-
Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data
Study
EGAS00001006388
-
Time-dependent characterization of CNS response in COVID-19
Study
EGAS00001006442
-
T cell reactivity of MHC epitopes
Study
EGAS00001006445
-
Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells
Study
EGAS00001004087
-
Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
Study
EGAS00001005071