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Single cell sequencing of endoscopic biopsies from Barrett's oesophagus and proximal tissue from the normal GI tract
Study
EGAS00001003144
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Genomic profiling of paediatric glioma cell lines
Study
EGAS00001003006
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Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
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SNP arrays for chemotherapy response project
Study
EGAS00001004519
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The Jerusalem Perinatal Study (JPS) aimed to examine the developmental origins of cardiometabolic risk.
Study
EGAS00001004075
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Genomic_landscape_of_liver_cirrhosis
Study
EGAS00001004329
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Whole genome sequencing of glioblastoma reveals enrichment of non-coding constraint mutations in known and novel genes
Study
EGAS00001004379
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Bulk RNAseq gene expression of baseline tumors from metastatic urothelial bladder cancer patients (IMvigor210) and metastatic renal cell carcinoma (IMmotion150)
Study
EGAS00001004386
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WES sequencing of malignant peripheral nerve sheath tumours
Study
EGAS00001004527
-
Gut microbiota analysis after 3months probiotic-like bacteria or placebo treatment in subjects with metabolic syndrome
Study
EGAS00001003585
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Novel PARN mutations in Hoyeraal-HReidarsson syndrome patients.
Study
EGAS00001003623
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Mutations conferring differential treatment response in breast cancer
Study
EGAS00001003626
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
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Genomic Signatures Reveal DNA Damage Response Deficiency in Brain Metastases of Colorectal Cancer
Study
EGAS00001003659
-
Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas
Study
EGAS00001003686
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Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
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Targeted panel data for newly diagnosed myeloma patients.
Study
EGAS00001002859
-
Mutational Landscape of Plasmablastic Lymphoma
Study
EGAS00001004906
-
Blood RNA-seq from Mexican DMD patients and healthy controls
Study
EGAS00001004907
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Discovering genetic causes of optic atrophy syndromes through whole exome sequencing
Study
EGAS00001003850