-
Molecular profiling of EBV associated diffuse large B-cell lymphoma
Study
EGAS00001006400
-
Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Study
EGAS00001006118
-
Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123
-
Genetic regulation of gene expression in human brain cell types
Study
EGAS00001006345
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
DNA methylation-based prognostic subtypes of chordoma tumors in tissue
Study
EGAS00001006406
-
Mapping genetic effects on cell type-specific chromatin accessibility using single nucleus ATAC-seq
Study
EGAS00001006184
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Study
EGAS00001003528
-
Long-term temporal stability of peripheral blood DNA methylation alterations in patients with inflammatory bowel disease.
Study
EGAS00001006501
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Study
EGAS00001006340
-
Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Study
EGAS00001003563
-
ATAC-seq/ChIP part
Study
EGAS00001006520
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
5- FU treated organoids
Study
EGAS00001003592
-
GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
Cystic fibrosis multi-omics study
Study
EGAS00001006421
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
Transcriptome profiling of three giant cell tumour of bone cell lines
Study
EGAS00001006441
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Study
EGAS00001006456
-
Histone modifications of cfDNA
Study
EGAS00001006503
-
Human adipose tissue immune cells
Study
EGAS00001003725
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Study
EGAS00001006643
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases
Study
EGAS00001006502
-
DERMATLAS__Tubular_adenoma
Study
EGAS00001006686
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
Neuroblastoma Evolution
Study
EGAS00001006533
-
cfDNA in Hereditary And High-Risk Malignancies (CHARM)
Study
EGAS00001006539
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
-
GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Data containing genome-wide SNP data from Northwestern Amazonia
Study
EGAS00001006767