About the database
The HelixMTdb database reflects aggregated and de-identified mitochondrial DNA variants observed in individuals sequenced at Helix. These individuals have not been sequenced based on the presence or absence of any medical phenotype (i.e. there are no inclusion or exclusion criteria in the registration process based on any medical phenotype).
Research using HelixMTdb
Selective constraints and pathogenicity of mitochondrial DNA variants inferred from a novel database of 196,554 unrelated individuals, Bolze* and Mendez* et. al., BioRxiv, October 8, 2019.
HelixMTdb presentation by Alexandre Bolze, Ph.D.
Helix Scientist Alexandre Bolze, Ph.D., recently presented the HelixMTdb at the 9th Human Genetics in NYC Conference. If you missed it, don't worry: You can download his presentation slides here. A similar talk can be seen below. Have questions? Fill out the contact form below to get in contact with us.
More from the Helix research team
We have many varied projects that are ongoing. You can learn more from our publications, posters, white papers, and more.
Listen to this brief talk from Helix scientist Alexandre Bolze to learn about the HelixMtDb and how it might be used.