-
BCR_repertoire_sequencing
Study
EGAS00001003185
-
Single-cell RNA sequencing of 6 follicular lymphoma tumors
Study
EGAS00001005257
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
Single-cell analysis for metastatic gastric adenocarcinoma
Study
EGAS00001004443
-
Integration of genomics and metabolomics in acute myeloid leukemia
Study
EGAS00001005422
-
Cell types of the human retina and its organoids at single-cell resolution. Cowan et al
Study
EGAS00001004561
-
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Study
EGAS00001004682
-
Detection of maternal DNA contamination in the placenta
Study
EGAS00001006155
-
UROMOL 2020 - SNP data
Study
EGAS00001004862
-
RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC
Study
EGAS00001005808
-
glioblastoma single cell RNAseq
Study
EGAS00001006236
-
GINS3 fibroblast RNAseq
Study
EGAS00001006038
-
Profiling of 27 type 2 diabetes GWAS loci using next-generation (NG) capture C in a human beta-cell model
Study
EGAS00001006105
-
Hereditary_Cerebellar_Ataxias___Whole_Genome_Sequencing___2021
Study
EGAS00001006234
-
RNA sequencing of NK cells in human lung
Study
EGAS00001003544
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
Whole-Exome Sequencing analyses in tamoxifen-associated endometrial cancer
Study
EGAS00001006453
-
Whole blood transcriptomic analysis of ANCA-associated vasculitis
Study
EGAS00001006704
-
Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis
Study
EGAS00001006632
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Study
EGAS00001006674
-
FFPE, buffycoat and cell free DNA from N. German esophagus cancer patients - 2021
Study
EGAS00001006813
-
The Landscape of N-6 Methyladenosine in Primary Localized Prostate Cancer
Study
EGAS00001006925
-
Multiomic Sequencing of Paired Primary and Metastatic Small Bowel Carcinoids
Study
EGAS00001006988
-
NEC
Study
EGAS00001007013
-
GWAS on covid-19 severity and susceptibility in the province of Bergamo, Italy
Study
EGAS00001007310
-
Possible DNA damage after paternal exposure to ionizing radiation in radar technicians
Study
EGAS00001007321
-
Epithelioid haemangioendothelioma (EHE) case series from the Stafford Fox Rare Cancer Program
Study
EGAS00001007474
-
RNA sequencing in primary human macrophages overexpressing ETS2
Study
EGAS00001007554
-
To_profile_the_landscape_of_sebaceous_tumours___RNA
Study
EGAS00001007803
-
Synthetic - GDI synthetic data
Study
EGAS50000000678
-
The cellular state space of AML unveils novel NPM1 subtypes with distinct clinical outcomes and immune evasion properties
Study
EGAS50000001084
-
Transcriptome analysis of a novel human iPSC-derived 3D cortical tissue model - WT, APP KI, Abeta-treated, Abeta/Aducanumab-treated
Dataset
EGAD50000002031
-
Benchmark Dataset for Somatic Mutation Calling in Cell-Free DNA
Dataset
EGAD50000001870
-
Profiling the genomic landscape and evolutionary history of polyploid giant cancer cells in undifferentiated pleomorphic sarcomas
Dataset
EGAD50000002084
-
EstMB cohort participants sequenced with MGISEQ-2000 platform
Dataset
EGAD50000002213
-
SCANDARE HNSCC 3' Tag RNA-seq
Dataset
EGAD50000001655
-
SCANDARE TNBC WES data
Dataset
EGAD50000001661
-
SCANDARE TNBC WGS data
Dataset
EGAD50000001662
-
Targeted Sequencing of 52 Genes for Severe COVID-19
Dataset
EGAD50000001378
-
Olink Explore Protein Expression
Dataset
EGAD50000001327
-
Indonesian Microbiome Ecology and Evolution v1 (raw data)
Dataset
EGAD50000001399
-
Whole genome and transcriptome sequencing of cancer of unknown primary tumours
Dataset
EGAD50000000656
-
Cergentis FFPE-TLC sequencing of colorectal carcinoma
Dataset
EGAD50000000618
-
Whole Exome Sequencing of controls performed at the Broad Institute on a cohort from Bristol, UK
Dataset
EGAD50000000716
-
Whole genome sequencing of pancreatic cystic fluid for early detection and diagnosis of pancreatic cancer
Dataset
EGAD50000000869
-
Alpha synucleinopathy spectrum - bulk RNA seq of prefrontal cortex
Dataset
EGAD50000000430
-
Alpha synucleinopathy spectrum - single nucleus RNA seq of prefrontal cortex
Dataset
EGAD50000000431
-
Complex-I stratification of Parkinson's disease - single nucleus RNAseq
Dataset
EGAD50000000432
-
Complex-I stratification of Parkinson's disease in the prefrontal cortex - bulk RNA seq
Dataset
EGAD50000000433
-
Dataset for study Genome-wide gene expression analysis following CRISPRi of transposable elements
Dataset
EGAD00001015689
-
Transcriptome Sequencing of Cancer Cell Lines
Dataset
EGAD00001000359
-
RNA sequencing data of pediatric TCF3::PBX1 acute lymphoblastic leukemia
Study
EGAS50000001797
-
WGBS data (CancerLocator study) of cell-free DNA derived from human blood
Dataset
EGAD00001003168
-
Whole exome sequencing for clarification of rare causes of axonal Charcot-Marie-Tooth disease (2017-08-16)
Dataset
EGAD00001003565
-
Identification of genes involved in congenital disorders of glycosylation and 3-methylglutaconic aciduria (2018-03-14)
Dataset
EGAD00001004038
-
Matched Pair Cell Line Tumour RNAseq
Dataset
EGAD00001000630
-
Genome-wide analysis of H3K27me3 occupancy and DNA methlytion in pediatric high-grade glioma
Dataset
EGAD00001000677
-
FFPE CPA Accreditation Study Part 2
Dataset
EGAD00001000868
-
Complete DNA/RNA sequencing dataset for Australian ICGC ovarian cancer sequencing project 2014-07-07
Dataset
EGAD00001000877
-
Genome-wide genotyping data and exome sequencing of 100 European-descent and 100 African-descent Belgians used in the EGAS00001001895 study
Dataset
EGAD00001002714
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)
Dataset
EGAD00001005017
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGBS)
Dataset
EGAD00001005018
-
RNA-seq study of longitudinal blood cell samples drawn from children at risk of type 1 diabetes
Dataset
EGAD00001005767
-
Breast Cancer Single-Cell RNA-Seq Dataset
Dataset
EGAD00001007495
-
Paired WES and low coverage WGS of osteosarcoma
Dataset
EGAD00001007509
-
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Dataset
EGAD00001007997
-
Deep targeted DNA sequencing dataset for the study "Molecular characteristics in Burkitt lymphoma over age groups"
Dataset
EGAD00001007708
-
Induction of trained immunity by influenza vaccine: impact on COVID-19
Dataset
EGAD00001007827
-
Resequencing candidate genes for male spermatogenic impairment
Dataset
EGAD00001006784
-
Combinatorial CRISPR screen identifies fitness effects of paralogues FAM50A and FAM50B
Dataset
EGAD00001006648
-
Cholangiocarcinoma
Dataset
EGAD00001008968
-
SPECIAL: scRNA-seq
Dataset
EGAD00001009291
-
Genome and transcriptome sequence data from a melanoma patient
Dataset
EGAD00001011022
-
Genome and transcriptome sequence data from a follicular lymphoma patient
Dataset
EGAD00001011023
-
Genome and transcriptome sequence data from a neuroendocrine tumor patient
Dataset
EGAD00001011024
-
Genome and transcriptome sequence data from a thymic cancer patient
Dataset
EGAD00001011025
-
Genome and transcriptome sequence data from a small cell lung carcinoma patient
Dataset
EGAD00001011026
-
Genome and transcriptome sequence data from a pancreatic cancer patient
Dataset
EGAD00001011027
-
Genome and transcriptome sequence data from a nasopharyngeal carcinoma patient
Dataset
EGAD00001011028
-
Genome and transcriptome sequence data from a colorectal carcinoma patient
Dataset
EGAD00001011029
-
Genome and transcriptome sequence data from a pancreatic adenocarcinoma patient
Dataset
EGAD00001011030
-
Genome and transcriptome sequence data from a urachal adenocarcinoma patient
Dataset
EGAD00001011031
-
Genome and transcriptome sequence data from a liposarcoma patient
Dataset
EGAD00001011032
-
Genome and transcriptome sequence data from a gastrointestinal stromal tumor patient
Dataset
EGAD00001011033
-
Genome and transcriptome sequence data from a granulosa cell ovarian tumor patient
Dataset
EGAD00001011034
-
Genome and transcriptome sequence data from a pancreatic adenocarcinoma patient
Dataset
EGAD00001011035
-
Genome and transcriptome sequence data from a metastatic breast cancer patient
Dataset
EGAD00001011036
-
Genome and transcriptome sequence data from a metastatic triple negative breast cancer patient
Dataset
EGAD00001011037
-
Genome and transcriptome sequence data from a papillary thyroid carcinoma patient
Dataset
EGAD00001011038
-
Genome and transcriptome sequence data from a thymoma patient
Dataset
EGAD00001011039
-
Genome and transcriptome sequence data from a rectal adenocarcinoma patient
Dataset
EGAD00001011040
-
Shallow whole genome sequencing
Dataset
EGAD00001011049
-
Combination Immune Checkpoint Inhibition in Australian Rare Cancers_WES
Dataset
EGAD00001015465
-
WGS/WES analysis refines molecular subtypes of hepatocellular carcinoma
Dataset
EGAD00001015428
-
The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Dataset
EGAD00001015503
-
Bulk RNA-seq dataset of Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Dataset
EGAD00001015508
-
ATAC-seq dataset of Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Dataset
EGAD00001015509
-
scRNA-seq dataset of Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts
Dataset
EGAD00001015510
-
PCA Atlas Visium spatial transcriptomics data (FASTQs, spaceranger BAMs and Visium mapping tables)
Dataset
EGAD00001015796
-
ecDNA copy number heterogeneity
Study
EGAS50000000509