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Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma - RNA
Dataset
EGAD00001015366
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scRNA-seq of total bone marrow and T cells from multiple myeloma long-term survivors
Dataset
EGAD00001010025
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Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
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WGS of OvCa
Dataset
EGAD00001008581
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RNA-seq data from 224 advanced prostate tumors generated by the West Coast Dream Team
Dataset
EGAD00001008487
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Southern African Prostate Cancer Study (SAPCS) Ethnic Disparity
Dataset
EGAD00001009067
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NuGen Targeted Sequencing of 574 DLBCL Cases of Non-China Cohort from Phoenix Clinical Trial
Dataset
EGAD00001008132
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Whole genome sequencing delineates regulatory and other genic variants in early onset cardiomyopathy
Dataset
EGAD00001008477
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WXS and RNA-seq raw sequence data for TG project
Dataset
EGAD00001007989
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RNA-seq data from 164 advanced prostate tumors generated by the West Coast Dream Team including 42 paired samles
Dataset
EGAD00001009065
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Influence of the Microbiome on Epigenetic Mechanisms in IBD
Dataset
EGAD00001011066
-
Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma - WES
Dataset
EGAD00001015365
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015477
-
The earliest stages of neoplastic transformation in Familial Adenomatous Polyposis
Dataset
EGAD00001015471
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SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
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Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
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FOXM1 is a biomarker of resistance to PI3Kα inhibition in ER+ breast cancer that is detectable using metabolic imaging (RNA-seq data)
Study
EGAS00001004452
-
Correction of a Factor VIII genomic inversion with designer recombinases
Study
EGAS00001005496
-
Genome wide association study of Coeliac Disease
Study
EGAS00000000057
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00000000052
-
Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development
Study
EGAS00000000029
-
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
Study
EGAS00000000056
-
Molecular Sub-grouping of CNS-PNET
Study
EGAS00000000116
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Clonally heritable gene expression imparts a layer of diversity within cell types
Study
EGAS50000000161