Industry Webinars & Resources
ASHG is pleased to offer members and professionals in human genetics and genomics resources like webinars, whitepapers, eBooks, and other scientific content. Some content has been sponsored to be featured on this page.
Disclaimer: By clicking on the following links, you may be directed to a form on the hosting company’s website where you may be asked to submit your contact information in order to download the content, and you may be contacted regarding your download and future interest in the company’s products or services. The hosting of any promotional material or links on the ASHG website does not indicate an endorsement by ASHG of the products or services promoted, the company, or the claims made. ASHG does not sell, rent, or share member contact information. Any information you choose to share will be shared with the company directly, and you may request to be removed from their mailing lists at any time.
Jump to: On-Demand Webinars | Webinars | Whitepapers
On-Demand Webinars
Investigating methylation in the human genome with Oxford Nanopore
Methylation plays an important role in regulating gene expression, with aberrant methylation in gene promoters associated with disease. Using nanopore sequencing, it is possible to prepare and sequence native DNA and RNA molecules, without the need for PCR. This enables the direct detection of intact methylation alongside nucleotide sequence — with no additional library prep steps. Long-range epigenetic changes, structural variants, and single nucleotide polymorphisms can be identified and phased in a single dataset. Sponsored by Oxford Nanopore Technologies
PacBio Neuroscience Day
Learn how highly accurate long-read sequencing can be used at every stage of your research, from disease variant identification to elucidation of the disease mechanisms and screening disease cohorts. Presentations range from rare undiagnosed disease to common complex disease, and methods presented range from whole genome sequencing to RNA sequencing (both bulk and single-cell) and various targeted sequencing methods. Sponsored by PacBio
How the Sequel IIe System Removes Barriers and Empowers Life Scientists
HiFi reads from PacBio are transforming sequencing. With their unique combination of high accuracy and long read lengths, HiFi reads produce superior results across a range of applications, from creation of reference-quality de novo assemblies, to comprehensive variant detection and full-length transcript sequencing. Moreover, HiFi data is easy to store and process, dramatically reducing compute and data storage needs. Learn how HiFi reads are empowering leading core labs and service providers, and how the new Sequel IIe System, which directly outputs HiFi reads, is making it easier than ever before to get started with HiFi reads or add capacity. Sponsored by PacBio
White Paper/eBook Resources
Chromium X Brochure | ebook | Sponsored by 10X Genomics
Essential Guide to Multiomic Immunology | ebook | Sponsored by 10X Genomics
Immunology EBook | ebook | Sponsored by 10X Genomics
Disclaimer: By clicking on the above links, you may be directed to a form on the hosting company’s website where you may be asked to submit your contact information in order to download the content, and you may be contacted regarding your download and future interest in the company’s products or services. The hosting of any promotional material or links on the ASHG website does not indicate an endorsement by ASHG of the products or services promoted, the company, or the claims made. ASHG does not sell, rent, or share member contact information. Any information you choose to share will be shared with the company directly, and you may request to be removed from their mailing lists at any time.