Listen to Oklahoma Medical Research Foundation’s core director, Graham Wiley, speak to all of the ways the NovaSeq X has made his lab’s research more efficient and cost saving.
Speaker
Graham Wiley, PhD
Core Director, Staff Scientist
Clinical Genomics Center, Oklahoma Medical Research Foundation
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Date & Time
Apr 23, 2024
Affiliation
Clinical Genomics Center, Oklahoma Medical Research Foundation
Individuals suspected of having a rare disease often face a long search for an answer. With up to 80% of rare diseases being genetic or having a genetic subtype, it is imperative to interrogate the genome to find answers and shorten the diagnostic odyssey. This webinar provides an overview of the integrated workflow provided by Illumina for rare and undiagnosed diseases research. Starting from library prep to sequencing and informatics, Illumina empowers researchers to find the answers they seek in rare and undiagnosed disease research.