-
Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Study
EGAS00001003388
-
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
-
Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Chromatin_accessability_in_cytokine_induced_immune_cell_states
Study
EGAS00001003501
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Genetic landscape of ENKTCL
Study
EGAS00001006906
-
Histone modifications of cfDNA
Study
EGAS00001006503
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
Indonesian methylation data
Study
EGAS00001003653
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002642
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002643
-
Genome-wide genetic and epigenetic dataset of pancreatic acinar cell carcinomas
Study
EGAS00001002533
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Submission 18 - study_title 1
Study
EGAS50000000365
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Submission 296 - study_title 2
Study
EGAS50000000392
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
Comprehensive genetic analysis of uveal melanoma heterogeneity during metastatic progression
Study
EGAS00001002761
-
BE_screens_of_WRN_gene_in_MSI_models
Study
EGAS00001006872
-
Spatial_transcriptome_analysis_of_Paediatric_Thymus
Study
EGAS00001004281
-
Swiss demo study
Study
EGAS50000000404
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
-
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
-
Exome_sequencing_of_a_Novel_Primary_T_Cell_Immunodeficiency_Kindred
Study
EGAS00001000099
-
Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse
Study
EGAS00001007128
-
Dissecting intratumor heterogeneity of nodal B cell lymphoma on the transcriptional, genetic, and drug response level
Study
EGAS00001004335
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Study
EGAS00001004316
-
Knee_OA_Functional_Genomics
Study
EGAS00001001899
-
Dataset that contains runs of submission 299
Dataset
EGAD50000000403
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component)
Study
EGAS00001001558
-
APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
A Universal Gut Metagenomic-Derived Signature Predicts Cirrhosis
Study
EGAS00001004600
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
Chromatin landscape of medulloblastoma reveals context dependent driver
Study
EGAS00001006741
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Study
EGAS00001006017
-
Genomic landscape of oral cancers (Illumina WGS)
Study
EGAS00001003228
-
Genomic characterization of a patient with AGS and CdLS transcriptomic comparison of his monocytes against healthy and disease control samples
Study
EGAS00001007829
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq)
Study
EGAS00001006016
-
Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis
Study
EGAS00001006632
-
Triple_Negative_Breast_Cancer_Whole_Genomes
Study
EGAS00001000092
-
Breast_Cancer_Somatic_Genetics_Study_
Study
EGAS00001000195
-
HER2_positive_Breast_Cancer_
Study
EGAS00001000042
-
Triple_Negative_Breast_Cancer_RNA_Sequencing
Study
EGAS00001000377
-
BASIS_RNAseq
Study
EGAS00001000707
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Study
EGAS00001005974
-
Unraveling Rare Genetic Variants: Insights from Whole-Genome Sequencing in Precision Medicine
Study
EGAS50000000373
-
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
Spatial and temporal genomic evolution in glioblastoma
Study
EGAS00001001033
-
Scalable whole-genome single-cell library preparation without pre-amplification
Study
EGAS00001002170
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Study
EGAS00001007555
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
-
The EGA at the International Congress of Human Genetics
Blog
the-ega-at-the-international-congress-of-human-genetics
-
Shedding light over COVID-19 susceptibility and severity
Blog
covid-19-susceptibility-and-severity
-
GCAT | Genomes for life
Blog
gcat-genomes-for-life
-
Providing access to COVID-19 data: one year later
Blog
providing-access-to-covid-19
-
The last addition to the list of clonal evolution studies in the EGA
Blog
the-last-addition-to-the-list-of-clonal-evolution-studies-in-the-ega
-
The Federated EGA network
Blog
the-federated-ega-network
-
Data upcycling, powered by EGA
Blog
data-upcycling-powered-by-ega
-
Youth-GEMs, the project using data to define the mental health trajectories of young people
Blog
youth-gems-mental-health
-
Papua New Guinean Genome Diversity Project
Study
EGAS00001005393
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007052
-
Dataset that contains runs of submission 117
Dataset
EGAD50000000166
-
Whole-genome-sequencing and Whole-exome-sequencing in Spastic paraplegia
Study
JGAS000494
-
Elucidating the development of cervical cancer and identifying therapeutic targets based on cancer genome analysis.
Study
JGAS000803
-
Genetic and epigenetic analysis of individuals with porokeratosis
Study
JGAS000684
-
Comprehensive survey for the construction of an integrated database of food, gut microbiome, and health information (the "Sukoyaka Health Survey").
A study on the relationship between food and health and genetic background.
Study
JGAS000679
-
Multi-omic profiling of patient-derived pancreatic tumor organoids
Study
JGAS000719
-
Amplicon sequencing of melanoma samples
Study
JGAS000351
-
Whole-exome-sequencing in Charcot-Marie-Tooth disease (CMT)
Study
JGAS000337
-
Biomarker Research for Anti EGFR Monoclonal Antibodies by Comprehensive Cancer Genomics
Study
JGAS000779
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000664
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000641
-
Unraveling the heterogeneity of multiple myeloma identifies therapy resistant subpopulation with vulnerability to the splicing pathway intervention
Study
JGAS000723
-
Application of organoid culture system of human gastrointestinal and thoracic cancer in genome medicine
Study
JGAS000653
-
Whole-exome-sequencing in Motor neuron disease (MND)
Study
JGAS000422
-
Cancer genomics for elucidation of molecular mechanisms of carcinogenecis and progression in lung cancer
Study
JGAS000756
-
Genetic analyses in patients with T or NK cells-associated disorders
Study
JGAS000709
-
In vitro reconstitution of epigenetic reprogramming in the human germ line
Study
JGAS000690
-
LEF1 knockdown effects on human T cell transcriptome and chromatin accessibility profiles.
Study
JGAS000818
-
Chromatin accessibility in stem cells unveils progressive transcriptional reprogramming in myelodysplastic syndrome
Study
JGAS000718
-
Comprehensive survey for the construction of an integrated database of food, gut microbiome, and health information (the "Sukoyaka Health Survey")
A data collection study exploring the relationship between the gut microbiome, food, health, and the genome.
Study
JGAS000680
-
Whole genome sequencing of human induced pluripotent stem cells derived from 5 type I cyctic biliary atresia patients
Study
JGAS000765
-
RNA-seq data of bone marrow CD34-positive cells from 57 patients with myelodysplastic syndromes (MDS) and 5 healthy individuals (62 participants in total)
Study
JGAS000724
-
Phenotype and genotype correlation analysis in tuberous sclerosis complex
Study
JGAS000688
-
Analysis of genes associated with autistic spectrum disorder, schizophrenia, and bipolar disorder.
Study
JGAS000731