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Study Description

This study describes the design, application and implementation of the NeuroChip genotyping platform. The NeuroChip (Illumina) is an affordable, high-throughput genotyping array that contains a tagging variant backbone (n ~ 300,000 variants) as well as manually curated custom variant content. These custom variants have been previously reported in diverse neurological diseases. We genotyped 273 neurologically healthy controls to assess genotyping performance and accuracy. Here, we release the raw genotype data of these control individuals.

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Study Inclusion/Exclusion Criteria

Neurologically normal control individuals only.

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Study Attribution
  • Principal Investigator
    • Andrew Singleton, PhD. Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
  • Co-Investigator
    • Sonja W. Scholz, MD, PhD. Neurodegeneration Diseases Research Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Funding Sources
    • Z01-AG000949-02 (Intramural Funding). National Institute of Neurological Disorders and Stroke, National Institute on Aging, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
    • Z01-ES101986 (Intramural Funding). National Institute of Neurological Disorders and Stroke, National Institute on Aging, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.
    • 1ZIANS003154 (Intramural Funding). National Institute of Neurological Disorders and Stroke, National Institute on Aging, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, MD, USA.