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Diamond Sponsors

The Simons Foundation Fund was set up on 18 September 1975 by the Dutch Anthropogenetic Society (NAV) with a legacy from J.E. Simons. The foundation’s aim is to encourage the study of human genetics and to promote and disseminate knowledge on hereditary diseases by sponsoring conference visits and providing financial support to young researchers for scientific visits.

Invitae offers affordable genetic testing and software for genetic analyses. At NVHG 2020, Invitae will be introducing the newest features of Moon, an innovative software package for genome interpretation that autonomously diagnoses rare diseases using artificial intelligence. The software reduces analysis time from days or weeks to mere minutes, making it the fastest variant interpretation software on the planet.

Golden Sponsors

PacBio delivers highly accurate long-read sequencing for the most comprehensive view of human genetic variation. With these HiFi reads and the Sequel II System, scientists can resolve complex regions with end-to-end solutions for exploring genomes and transcriptomes. Click on our logo to learn more. 

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

BGI Genomics is one of the world’s leading providers of genomic sequencing services and proteomic services, now serving customers in more than 66 countries. We have over 20 years of genomics experience helping our customers achieve their research goals by delivering rapid, high quality results using a broad array of cost-effective, cutting-edge technologies.

The Illumina mission is to improve human health by unlocking the power of the genome. Now, through innovation and collaboration, we are enabling genomic breakthroughs and helping simplify the patient diagnostic odyssey with whole-genome sequencing. The discoveries we know lie ahead for rare and undiagnosed genetic diseases are what inspire us to push the boundaries and drive innovation.

PacBio delivers highly accurate long-read sequencing for the most comprehensive view of human genetic variation. With these HiFi reads and the Sequel II System, scientists can resolve complex regions with end-to-end solutions for exploring genomes and transcriptomes. Click on our logo to learn more. 

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

BGI Genomics is one of the world’s leading providers of genomic sequencing services and proteomic services, now serving customers in more than 66 countries. We have over 20 years of genomics experience helping our customers achieve their research goals by delivering rapid, high quality results using a broad array of cost-effective, cutting-edge technologies.

The Illumina mission is to improve human health by unlocking the power of the genome. Now, through innovation and collaboration, we are enabling genomic breakthroughs and helping simplify the patient diagnostic odyssey with whole-genome sequencing. The discoveries we know lie ahead for rare and undiagnosed genetic diseases are what inspire us to push the boundaries and drive innovation.

Silver Sponsors