Unlocking precision: The power of PIPseq V in scRNA-Seq
ASHG: Fluent CoLab
Details
PIPseq V represents the cutting edge of single cell sequencing technology, offering accuracy and accessibility in biological insights and data analysis. In this talk, we’ll explore how PIPseq V enables researchers to delve deeper into the complexities of the genome, with a scalable, accessible solution. Through customer data and insights, we’ll showcase the developing possibilities of single cell research.
Joel Fellis, PhD
VP, Product Management
Illumina
Shane A. Liddelow, PhD
Associate Professor, Department of Neuroscience and Physiology
Associate Professor, Department of Ophthalmology
NYU
M-AMR-01699
Fill Out Form to Access Webinar
Your email address is never shared with third parties.
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.