-
DNA methylation repeatability in the Lothian Birth Cohorts of 1921 and 1936.
Study
EGAS00001000910
-
WTCCC3_Anorexia_Nervosa
Study
EGAS00001000913
-
APCDR AGV Project: Whole genome sequencing of 3 African populations (curated data)
Study
EGAS00001000960
-
Exome_sequencing_in_patients_with_cardiac_arrhythmias
Study
EGAS00001000063
-
SOFT_study___sequencing_premenopausal_breast_cancer
Study
EGAS00001000983
-
Whole genome sequencing of ASD quartet families
Study
EGAS00001001023
-
Intratumor heterogeneity evaluation in primary HCC cells
Study
EGAS00001001135
-
APCDR AGV Project: The African Genome Variation Project(dense array genotyping data)
Study
EGAS00001000959
-
Colorectal_Adenoma_Gene_Screen
Study
EGAS00001001261
-
cis-eQTL mapping of human pancreatic islets
Study
EGAS00001001265
-
Korean Young Age Diffuse Gastric Cancers
Study
EGAS00001001711
-
PRDM9_loss_of_function_follow_up_from_Born_in_Bradford_Autozygosity_sequencing
Study
EGAS00001001301
-
Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
-
CML_blast_phase_rearrangement_screen
Study
EGAS00001000191
-
Deep_sequencing_analysis_of_human_iPSC_specific_SNVs_in_donor_cell_population
Study
EGAS00001000373
-
Genetic subclone heterogeneity of tumor-initiating cells in human colorectal cancer
Study
EGAS00001001857
-
Maastricht IBS 16S data
Dataset
EGAD00001007074
-
NGS data of human NES cells and tumors
Dataset
EGAD00001004990
-
RNA-seq BAM files from newborn screening dried blood spot samples
Dataset
EGAD00001005009
-
RNA-seq of cultured human hematopoietic stem and progenitor cells from umblical cord blood in cytokine-rich ex vivo culture conditions following sphingolipid modulation
Dataset
EGAD00001005140
-
Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA
Dataset
EGAD00001005316
-
RNA-seq study of longitudinal blood cell samples drawn from children at risk of type 1 diabetes
Dataset
EGAD00001005767
-
Somatic mutation and clonal evolution in premalignant lung disease - WGS (2020-01-15)
Dataset
EGAD00001005786
-
Exome sequences of AL amyloidosis (ALA), multiple myeloma (MM) and ALA+MM hematological malignancies
Dataset
EGAD00001006047
-
Profiling heterogeneity in Human derived IPSC-neurons (2020-05-18)
Dataset
EGAD00001006157
-
Combinatorial CRISPR screen identifies fitness effects of paralogues FAM50A and FAM50B
Dataset
EGAD00001006648
-
RNAseq data of polyA+ RNA from Leukocytes from 624 individuals of the ProgeNIA cohort.
Dataset
EGAD00001003102
-
Cell of Origin and Early Evolution of Leukemia in Down Syndrome
Dataset
EGAD00001006555
-
Identification of genes involved in congenital disorders of glycosylation and 3-methylglutaconic aciduria (2018-03-14)
Dataset
EGAD00001004038
-
UMCU_Molpheno_Restricted
Dataset
EGAD00001004865
-
Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures
Dataset
EGAD00001006671
-
Resequencing candidate genes for male spermatogenic impairment
Dataset
EGAD00001006784
-
Single cell transcriptomic data of human gut macrophages
Dataset
EGAD00001007765
-
Anaplastic Oligodendroglioma AO Exome-seq data
Dataset
EGAD00001001452
-
RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC
Dataset
EGAD00001008356
-
Breast Cancer Single-Cell RNA-Seq Dataset
Dataset
EGAD00001007495
-
Genome-wide genotyping data and exome sequencing of 100 European-descent and 100 African-descent Belgians used in the EGAS00001001895 study
Dataset
EGAD00001002714
-
Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures
Dataset
EGAD00001006326
-
RNA-seq of non-LPS treated (N), non-tolerized (NT), and tolerized (T) IFNg-primed macrophages pretreated with or without HDAC3i
Dataset
EGAD00001005959
-
Variant calls for "Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients"
Dataset
EGAD00001005772
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002696
-
BAM files: Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Dataset
EGAD00001003806
-
Variant calling analysis of cfDNA whole exome sequencing in neuroblastoma
Dataset
EGAD00001003803
-
Exome sequencing of thyroid disease in Val Borbera
Dataset
EGAD00001000729
-
Genome Diversity in Africa Project - ancient samples - standard libraries
Dataset
EGAD00001002211
-
Paired WES and low coverage WGS of osteosarcoma
Dataset
EGAD00001007509
-
WGBS data (CancerLocator study) of cell-free DNA derived from human blood
Dataset
EGAD00001003168
-
MultiOMICS study of a pair of infant monozygotic twins with concordant B-cell ALL (WGS)
Dataset
EGAD00001005017
-
single cell RNA-seq of bone marrow from infants with MLL-rearranged Acute Lymphoblastic Leukemia by single cell RNA-sequencing
Dataset
EGAD00001005461
-
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Dataset
EGAD00001007969
-
Low coverage whole-genome sequencing of samples from the Cretan Greek isolate collection HELIC-MANOLIS
Dataset
EGAD00001001637
-
Lung cancer organoids
Dataset
EGAD00001004013
-
SNV and indel calls from 8086 individuals in the British Autozygosity Populations BioResource dataset
Dataset
EGAD00001004581
-
The Natural History of Human Prostate Cancer
Dataset
EGAD00001000689
-
TGS - Comprehensive Molecular Characterization of Colorectal Cancer Metastases (2015-07-02)[MOSAIC]
Dataset
EGAD00001001426
-
Whole exome sequencing for clarification of rare causes of axonal Charcot-Marie-Tooth disease (2017-08-16)
Dataset
EGAD00001003565
-
Complete DNA/RNA sequencing dataset for Australian ICGC ovarian cancer sequencing project 2014-07-07
Dataset
EGAD00001000877
-
single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes
Dataset
EGAD00001005768
-
Acquisition of additional mutations drives accelerated progression of NPM1 positive CMML to AML
Dataset
EGAD00001002194
-
chronic myelomonocytic leukemia (CMML)
Dataset
EGAD00001007026
-
Total RNA sequencing of 32 chronic lymphocytic leukemia (CLL) patients
Dataset
EGAD00001004047
-
RNA-seq of human iPSC-derived neurons to explore cellular phenotypes associated with schizophrenia.
Dataset
EGAD00001004064
-
Miseq (18S) analysis of spiked placental tissue samples
Dataset
EGAD00001004197
-
sWGS of Pap test smears from healthy donors and HGSOC patients and matched tumor tissue
Study
EGAS00001007084
-
Molecular subtypes of malignant peritoneal mesothelioma
Study
EGAS00001002820
-
Inference_of_B_cell_clonality_and_function_from_single_cell_RNA_seq_data
Study
EGAS00001002963
-
Exome sequencing of advanced hepatocellular carcinoma
Study
EGAS00001003130
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Exome_
Study
EGAS00001003316
-
Clonal_selection_after_gene_therapy_in_SCD___Duplex_sequencing
Study
EGAS00001007253
-
The genomic landscape of recurrent ovarian high grade serous carcinoma: the BriTROC-1 study
Study
EGAS00001007292
-
Intercellular nanotube-mediated mitochondrial transfer enhances T-cell metabolic fitness and antitumor efficacy
Study
EGAS00001007356
-
Prevalence of transthyretin amyloidosis in patients with heart failure and no left ventricular hypertrophy
Study
EGAS00001005398
-
Much ado about nothing? - Off-target amplification can lead to false positive bacterial brain microbiome detection in healthy and Parkinson's disease individuals
Study
EGAS00001004757
-
GWAS on covid-19 severity and susceptibility in the province of Bergamo, Italy
Study
EGAS00001007310
-
IgCaller
Study
EGAS00001004298
-
Exome sequencing of HCV+ lymphoma
Study
EGAS00001006860
-
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Study
EGAS00001005064
-
PELICAN45 RNAseq Dataset
Study
EGAS00001006959
-
Multiomic Sequencing of Paired Primary and Metastatic Small Bowel Carcinoids
Study
EGAS00001006988
-
RNA sequencing in primary human macrophages overexpressing ETS2
Study
EGAS00001007554
-
In this study, we performed exon sequencing (WXS) of 80 paired Brain cancer tumors and adjacent normal tissues to identify novel potential biomarkers. We extracted mutational signatures which induce somatic mutations . Our study covers a comprehensive genetic framework that can be used in clinical trials and treatment modalities in Brain cancer.
Study
EGAS00001002352
-
Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002576
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Study
EGAS00001002657
-
Whole-genome sequencing reveals genomic signatures associated with the inflammatory microenvironments in Chinese NSCLC patients
Study
EGAS00001002954
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__BRCA_Carriers__Targeted_
Study
EGAS00001003315
-
High Altitude Pulmonary Hypertension
Study
EGAS00001003171
-
WGS and WES of pediatric osteosarcoma
Study
EGAS00001003342
-
The genomic landscape of follicular and diffuse large B-cell lymphoma
Study
EGAS00001002199
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
Circulating tumor cell copy-number heterogeneity in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors
Study
EGAS00001005301
-
Landscape of somatic mutations and DNA copy number alterations and transcriptomic profiling identifies metabolic reprogramming as a hallmark of ibrutinib resistance
Study
EGAS00001003418
-
Copy-number signatures and mutational processes in ovarian carcinoma
Study
EGAS00001002557
-
TRACERx 100: RNAseq data from the first 100 TRACERx tumours
Study
EGAS00001003458
-
Himalayan_population_genetic_study
Study
EGAS00001002731
-
Genomic and epigenomic insights into the origin, pathogenesis and clinical behavior of mantle cell lymphoma subtypes
Study
EGAS00001004165
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Cancer_Mastectomy__Targeted_
Study
EGAS00001003318
-
WGS/RNA-seq pair of an inflammatory hepatocellular adenoma (IHCA)
Study
EGAS00001003025
-
Tetralogy of fallot whole-exome sequencing
Study
EGAS00001003302
-
Spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma
Study
EGAS00001007981
-
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms
Study
EGAS00001003486
-
Genomic study of an AT-AML
Study
EGAS00001004392
-
Immunogenomic landscape of hematological malignancies
Study
EGAS00001004444
-
To_profile_the_landscape_of_sebaceous_tumours_WES
Study
EGAS00001003553
-
Breast Cancer - immune clusters - RNA-seq
Study
EGAS00001003631
-
Prime editing for functional repair in patient-derived disease models
Study
EGAS00001004611
-
Exome sequencing of DNA from pituitary neuroendocrine tumor (PitNET) and germline DNA from the same patient
Study
EGAS00001004654
-
UROMOL 2020 - RNA-seq data
Study
EGAS00001004693
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (mouse)
Study
EGAS00001004696
-
Paediatric_CNS_tumour_autopsy_DNA
Study
EGAS00001004771
-
RNAseq of 76 samples from Uveal Melanoma tumors
Study
EGAS00001002932
-
Identification of recurrent mutations in Cushing’s disease
Study
EGAS00001003029
-
Spatial Heterogeneity in CLL
Study
EGAS00001003803
-
Functional analysis of GATA2 synonymous mutations
Study
EGAS00001003817
-
Nuclease deficiencies alter plasma cell-free DNA methylationprofiles (Human)
Study
EGAS00001004897
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Study
EGAS00001002439
-
Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma
Study
EGAS00001002517
-
Whole genome sequencing of patients affected by acute intermittent porphyria
Study
EGAS00001004999
-
Comparative genomics research for Chinese colorectal cancer
Study
EGAS00001002607
-
Molecular characterization of endothelial cells under conditions associated with hematopoietic niche formation in humans
Study
EGAS00001002736
-
scRNA_seq_of_circulatory_immune_cells_from_Crohn_s_disease_patient_blood
Study
EGAS00001004150
-
Multi-omics profiling of paired primary and recurrent glioblastoma patient tissues
Study
EGAS00001004345