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Genome Asia 100K Project
Study
EGAS00001002921
-
The genomic landscape of lung adenocarcinoma in East Asians
Study
EGAS00001002941
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
Colorectal advanced adenomas NKI-AvL TGO COCOS series
Study
EGAS00001002952
-
Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Study
EGAS00001002953
-
To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
-
Interethnic comparability in blood pressure GWAS
Study
EGAS00001002991
-
WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
HELIUS cohort
Study
EGAS00001002969
-
Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
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Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
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Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
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Epigenetic profiling of colorectal cancer initiating cells (CC-ICs) to identify bivalently marked genes (H3K4me3 and H3K27me3 ChIP-seq), and investigation of changes in transcriptome following EZH2 inhibition using RNA-seq.
Study
EGAS00001003003
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CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
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Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003137
-
Open_Targets_020_Epigenomes_of_Cell_Lines
Study
EGAS00001003139
-
Comprehensive genetic analysis of Epstein-Barr virus-associated hematological malignancy
Study
EGAS00001003159
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
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A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
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A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Study
EGAS00001003177
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Analysis of IDHwt-glioblastoma samples from paired primary and recurrent tumor samples
Study
EGAS00001003184
-
The_identification_of_genetic_vulnerabilities_in_head_and_neck_cancers_for_the_development_of_novel_therapies
Study
EGAS00001002204
-
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease
Study
EGAS00001002275
-
Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort
Study
EGAS00001002499
-
Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
-
Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers
Study
EGAS00001002604
-
Whole exome sequencing of 76 individuals with familial atrial fibrillation
Study
EGAS00001003207
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FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
-
Genomic landscape of oral cancers (Illumina WGS)
Study
EGAS00001003228
-
An exome sequencing approach to defining the genetic risk factors for Achilles tendinopathy
Study
EGAS00001003234
-
A mechanistic classification of clinical phenotypes in neuroblastoma
Study
EGAS00001003244
-
46 CLL Whole Genome Sequencing Study
Study
EGAS00001003254
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
-
Summary statistics from genome-wide association study in glioma of 12,488 cases and 18,169 controls.
Study
EGAS00001003372
-
A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Study
EGAS00001006547
-
H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
-
Embryonic tumour transmission in monozygotic twins
Dataset
EGAD00001015681
-
Duplexseq of the interstrand crosslinks_WGS
Dataset
EGAD00001010298
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - RNA-Seq
Dataset
EGAD00001009794
-
Exome Atlas in HCC tumors
Dataset
EGAD00001015342
-
Exome Sequencing of 44 subjects with very severe or fatal COVID-19
Dataset
EGAD00001008993
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Dataset
EGAD00001009668
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Dataset
EGAD00001009647
-
Anthropological dataset 1 for The admixture histories of Cabo Verde
Dataset
EGAD00001008976
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities - WGS
Dataset
EGAD00001009793
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia
Dataset
EGAD00001009304
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia - RNA
Dataset
EGAD00001009305
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Dataset
EGAD00001009847
-
Population-based analysis of POT1 variants in a cutaneous melanoma case-control cohort
Dataset
EGAD00001009848
-
Somatic mutation and clonal evolution normal breast tissue WGS
Dataset
EGAD00001010123
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (tumour data)
Dataset
EGAD00001010274
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - WGS
Dataset
EGAD00001010872
-
Anthropological dataset 2 for The admixture histories of Cabo Verde
Dataset
EGAD00001008977
-
Clonal origin of lineage switch leukemia following CAR-T cell and blinatumomab therapy
Dataset
EGAD00001009161
-
Oropharyngeal Squamous Cell Carcinoma Mutanome
Dataset
EGAD00001009167
-
Linguistic utterance counts for The admixture histories of Cabo Verde
Dataset
EGAD00001008978
-
Epigenomic analysis of human dopaminergic neuron differentiation reveals LBX1, NHLH1 and NR2F1/2 as necessary for lineage specification
Dataset
EGAD00001009288
-
Single-cell study of 14 childhood medulloblastoma patients
Dataset
EGAD00001009057
-
Convergent somatic evolution from early life in a germline ribosomopathy
Dataset
EGAD00001009061
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - WGS
Dataset
EGAD00001011645
-
RNAseq data
Dataset
EGAD00001009728
-
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Dataset
EGAD00001009280
-
HELIUS cohort gut microbiome batch2
Dataset
EGAD00001009732
-
Tracking the evolution of esophageal squamous cell carcinoma under dynamic immune selection by multi-omics sequencing
Dataset
EGAD00001009482
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - RNA
Dataset
EGAD00001009813
-
Human Origins array data for 1510 individuals
Dataset
EGAD00001010015
-
Genomic Analysis of a Metastatic Fusion-negative Embryonal Rhabdomyosarcoma
Dataset
EGAD00001009973
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Dataset
EGAD00001010103
-
Tumour evolvability metrics predict recurrence in advanced localised prostate cancer (normal data)
Dataset
EGAD00001010295
-
CRUK-ICGC Prostate DNA Methylation Sequencing Dataset (Prostatectomy Batches 1-6)
Dataset
EGAD00001010184
-
Raw data for "Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse"
Dataset
EGAD00001010260
-
Clonal dynamics after allogeneic haematopoietic cell transplantation using genome-wide somatic mutations - TGS
Dataset
EGAD00001010874
-
Clonal selection after gene therapy in sickle cell disease
Dataset
EGAD00001010913
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183
-
Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Longitudinal RNA-seq datasets from patients after abdominal surgery
Dataset
EGAD00001011102
-
Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
-
Capture-based NGS
Dataset
EGAD00001011151
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Dataset
EGAD00001011260
-
Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Dataset
EGAD00001011340
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Dataset
EGAD00001011067
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Dataset
EGAD00001011363
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma RNA
Dataset
EGAD00001014790
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
Exome sequencing of UK Birth Cohorts - Born in Bradford
Dataset
EGAD00001015370
-
Exome sequencing of UK Birth Cohorts - Millennium Cohort Study
Dataset
EGAD00001015372