-
Breast Cancer - Very young women
Study
EGAS00001001908
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
Lethal malformation syndrome
Study
EGAS00001000061
-
The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis
Study
EGAS00001001035
-
Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
-
Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Study
EGAS00001004274
-
Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Study
EGAS00001004534
-
Leucocyte eQTLs in autoimmune disease and health
Study
EGAS00001001251
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
TMD_AMKL_targeted_follow_up
Study
EGAS00001000569
-
HipSci___RNAseq___Rare_BBS
Study
EGAS00001001318
-
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Study
EGAS00001003598
-
COMPARE study: participants typed during UK Biobank version 2 array development phase
Study
EGAS00001003748
-
Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium
Study
EGAS00001001180
-
TMD_AMKL_targeted_follow_up_part_2
Study
EGAS00001000732
-
A WTCCC2 genome-wide association study for psychosis endophenotype (PE) in individuals from UK, Germany, Holland, Spain and Australia.
Study
EGAS00001000817
-
Transcriptomics_of_human_olfactory_mucosa
Study
EGAS00001001486
-
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Study
EGAS00001000085
-
The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Study
EGAS00001002709
-
Natural variation of circulating RNAs in human serum
Study
EGAS00001002814
-
Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia
Study
EGAS00001002827
-
Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Study
EGAS00001000455
-
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
CCND1-negative MCL
Study
EGAS00001003060
-
Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
-
DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ.
Study
EGAS00001000558
-
Role_of_Epigenetic_Memory_in_Human_Induced_Pluripotent_Stem_Cells_Pilot
Study
EGAS00001000742
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Study
EGAS00001003321
-
Microsatellite unstable colorectal cancers
Study
EGAS00001003366
-
Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000687
-
Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
-
Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML)
Study
EGAS00001003453
-
Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
-
Fetal hemoglobin in sickle cell disease patients from Tanzania
Study
EGAS00001000990
-
Congenital_anosmia_1
Study
EGAS00001001124
-
HipSci___RNAseq___Rare_Monogenic Diabetese
Study
EGAS00001001137
-
Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Study
EGAS00001004422
-
Understand_Paratyphoid_Disease___host_responses_to_human_challenge_with_S__Paratyphi_A
Study
EGAS00001001260
-
Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
-
SNP genotyping data in genes related to trace element homeostasis
Study
EGAS00001001292
-
Breast Cancer - Subtype defined by an amplification of the HER2 gene
Study
EGAS00001001431
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Indonesian Genome Diversity Project 2
Study
EGAS00001003654
-
Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy
Study
EGAS00001004894
-
Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Study
EGAS00001004697
-
Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
-
HCA_Female_Reproductive_Adult_WSSS_RNA
Study
EGAS00001004727
-
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
-
Premalignant SOX2 overexpression in the fallopian tubes of ovarian cancer patients: Discovery and validation studies
Study
EGAS00001001909
-
Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
-
Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
-
The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
-
Progression to AML is predictable and distinct from age related clonal hematopoiesis
Study
EGAS00001002570
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
-
Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Study
EGAS00001002866
-
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
-
Long cell-free DNA molecules in maternal plasma
Study
EGAS00001005515
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
Study
EGAS00001004888
-
Whole exome sequencing on Pediatric MDS patients
Study
EGAS00001005432
-
Single-cell DNA sequencing on Pediatric MDS
Study
EGAS00001005433
-
Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment.
Study
EGAS00001004123
-
Panbody_nanoseq
Study
EGAS00001005521
-
COVID_19_UK_CIC_Spatial
Study
EGAS00001005817
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Study
EGAS00001005941
-
Paediatric_and_adult_nasal_RNAseq___COVID19
Study
EGAS00001004391
-
Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
Study
EGAS00001005530
-
Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
-
Human Developmental Biology Resource (HDBR) abnormal fetal samples
Study
EGAS00001006300
-
Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes
Study
EGAS00001006068
-
molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer
Study
EGAS00001006350
-
Juntendo Muscle Study (JMS)
Study
EGAS00001006362
-
Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
-
Muscle SATellite cell study (MSAT)
Study
EGAS00001006363
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Study
EGAS00001005793
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
-
Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
-
scRNA-seq of patient-derived PDAC organoids and matched CAFs
Study
EGAS00001006661
-
Measurement of SARS-CoV-2 variants fraction in infected alveolar cells
Study
EGAS00001006730
-
scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Study
EGAS00001006787
-
Characterization of chromatin accessibility in metastatic prostate cancer
Study
EGAS00001006698
-
Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Study
EGAS00001006913
-
Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia
Study
EGAS00001006967