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Assembly of 809 whole mitochondrial genomes with clinical, imaging, and fluid biomarker phenotyping
INTRODUCTION: Mitochondrial genetics are an important but largely neglected area of research in Alzheimer’s disease. A major impediment is the lack of data sets. METHODS: We used an innovative, rigorous approach, combining several existing tools with our own, to accurately assemble and call variants...
Autores principales: | Ridge, Perry G., Wadsworth, Mark E., Miller, Justin B., Saykin, Andrew J., Green, Robert C., Kauwe, John S. K. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5961720/ https://www.ncbi.nlm.nih.gov/pubmed/29306584 http://dx.doi.org/10.1016/j.jalz.2017.11.013 |
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