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Genetic_variation_in_Kuusamo
Study
EGAS00001000020
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Whole genome sequencing data of pediatric B-other subtype acute lymphoblastic leukemia
Study
EGAS50000001497
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An isoform quantitative trait locus in SBNO2 links genetic susceptibility to Crohn’s disease with defective antimicrobial activity
Study
EGAS50000000183
-
WES in HCCOs with varying Doxorubicin resistance
Study
EGAS50000000043
-
IL-27 promotes tumour control by enhancing cytotoxic T cell function
Study
EGAS50000000694
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Djerroudi et al., E-cadherin inactivation shapes tumor microenvironment specificities in invasive lobular carcinoma
Study
EGAS50000000761
-
RNA sequencing data of pediatric B-other acute lymphoblastic leukemia
Study
EGAS50000001803
-
CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia
Study
EGAS00001004116
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CD36 defines CML cells less sensitive to imatinib
Study
EGAS00001002421
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
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Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci
Study
EGAS00001002592
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Functional screening on patient-derived organoids identifies a therapeutic bispecific antibody that triggers EGFR degradation in LGR5+ tumor cells
Study
EGAS00001004584
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Biallelic HMBS Inactivation Defines a Homogenous Clinico-Molecular Subtype of Hepatocellular Carcinoma
Study
EGAS00001005986
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
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Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
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Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer
Study
EGAS00001005952
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Proteogenomics reveals two distinct biological pilocytic astrocytoma subgroups
Study
EGAS00001006402
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Upper cortical layer-driven network impairment in schizophrenia
Study
EGAS00001006495
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Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing
Dataset
EGAD00001006088
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Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021)
Study
EGAS00001006706
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deCODE Genetics study on genes contributing to nicotine dependence in humans
Study
phs000393
-
Human Lung Tissue eQTL Study
Study
phs001745
-
A New High-Throughput Sequencing-Based Technology to Study Heterochromatin Structure
Study
phs002202
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Multimodal Mapping of the Immune Landscape in Human Pancreatic Cancer
Study
phs002071
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Prevention of Viral Hepatitis and HIV in Drug Users - A Hepatitis B Model for HIV and an HB Vaccine Model for HIV Vaccine Trials in Drug Users (DASH)
Study
phs002331
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TCGA WGS Variants Across 18 Cancer Types
Study
phs003155
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Somatic Mutations in Epilepsy: Whole Genome Sequence Analysis of Single Neurons
Study
phs002615
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3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
Study
JGAS000159
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Identifying autosomal recessive mutations causing neurological disorders
Study
EGAS00001000023
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Transcriptomic analysis of B-cell acute lymphoblastic leukaemia (B-ALL) patients treated on the ALL09 clinical trial
Study
EGAS50000001109
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Recording physiological history of cells with chemical labeling.
Study
EGAS50000000056
-
Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes
Study
EGAS50000000279
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RNA sequencing data from glioblastoma primary cell lines treated with indisulam
Study
EGAS50000000680
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Clinical relevance of TCGA subtypes for gastric cancer patients
Study
EGAS50000000779
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MATISSE bulk RNA-sequencing data
Dataset
EGAD50000001470
-
Inferring causal genes at type 2 diabetes GWAS loci through chromosome interactions in islet cells
Dataset
EGAD50000000517
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Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
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A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
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ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
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Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
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Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
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WGS of liver cancer in the Japanese population
Study
EGAS00001000678
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Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Study
EGAS00001001234
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Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
Study
EGAS00001002632
-
A benchmarking resource for NGS testing of cancer predisposition genes
Study
EGAS00001002993
-
Patient-derived organoids as a novel tool to study cervical cancer
Study
EGAS00001004439
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Characterization of genomic landscape of Peripheral T-cell Lymphomas, not otherwise specified (PTCL-NOS) (2018-10-30)
Dataset
EGAD00001004428
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IMCISION RNAseq
Study
EGAS00001005454
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Leveraging Extended Families for Cardiovascular Disease Genomic Discovery
Study
phs002464