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• Samples from the Greek island of Crete, MANOLIS cohort

  Whole-genome sequencing at 4x of 250 samples from the Greek isolatecollection HELIC

  Dataset EGAD00001001636

• Covacta OLINK NPX

  Olink Explore 1536 dataset from serum of patients enrolled in the COVACTA trial. This dataset includes the NPX values provided by Olink.

  Dataset EGAD00001011169

• Whole exome sequencing and RNA-seq of esophageal squamous cell carcinoma

  We perform integrative genome-wide analyses such as whole-exome sequencing, copy number variant(CNV) analysis, and gene expression analysis using next-generation sequencing and other methods to elucidate driver genes and signaling pathways causing tumorigenesis and cancer progression, leading novel molecular diagnostics and molecular therapies.

  Study JGAS000367

• Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia

  Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia

  Dataset EGAD00001000291

• Whole_Exome_Sequencing_of_INTERVAL

  Whole exome sequencing of a subset of participants from the INTERVAL study.

  Study EGAS00001000825

• Brain_Disease_Wellcome_Leap_Delta_Tissue_RNA

  Utilising Single-Nucleus sequencing to investigate how the tumour microenvironment regulates glioblastoma cell states.

  Study EGAS00001005800

• Exome sequences of three individuals from the EXCEED study

  Exome sequences of three unrelated individuals of south Asian ancestry from the EXCEED study

  Dataset EGAD00001007649

• BCG-Flu_Challenge_Study_RNAseq_Human_01

  RNA sequencing data generated from human samples collected in the BCG-Flu Challenge study.

  Study EGAS50000001677

• Genomic and transcriptomic profiling of combined hepatocellular and intrahepatic cholangiocarcinoma reveals distinct molecular subtypes

  We performed genomic and transcriptomic sequencing of 133 combined hepatocellular and intrahepatic cholangiocarcinoma (cHCC-ICC) cases, including separate, combined, and mixed subtypes.

  Study EGAS00001003093

• The study provides comprehensive access to the set of EGA studies which may be useful as controls.

  The subjects studies in these datasets were selected due to being healthy control individuals or otherwise provide well characterised phenotype or exclude certain disease phenotype categories such that they may be useful as control population, such as to derive allele frequencies from a known reference population.

  Study EGAS00001000646