Archives: Videos
Revio and Onso – long-read and short-read sequencing with exceptional accuracy
The Revio long-read sequencer introduces long reads at a lower cost and higher throughput. The Onso short-read sequencer delivers short reads with near-perfect accuracy.
Combined, the completeness of long reads with the accuracy of short reads provides the most comprehensive view of genomes, transcriptomes, and epigenomes.
Revio system by PacBio – reveal more with accurate long-read sequencing at scale
The Revio system adds affordability, high throughput, and ease of use to a foundation of long reads, exceptional accuracy and direct methylation detection.
Onso system by PacBio – a new standard in short-read sequencing
The Onso system is an innovative benchtop short-read DNA sequencing platform with an unprecedented level of accuracy using PacBio sequencing by binding (SBB) technology. Ultra-high Q40+ data quality allows you to break through limits of detection.
Highly Accurate HiFi Reads for Discovery, Design, and Manufacturing of AAV Gene Therapy
Gene therapy is at an inflection point and experiencing tremendous growth. High accuracy and complete visibility are critical to the success of novel vector discovery, vector design, and manufacturing quality control for gene therapy products. This webinar illustrates why PacBio HiFi sequencing is the ideal solution due to its ability to sequence full length AAV genomes at high accuracy, which allows for detection of fragmentation, mutations, and large structural events. Short reads, qPCR, and less accurate long-read technology can miss important changes that may be present in the AAV sequence, potentially affecting the safety and efficacy of gene therapy products.
HiFi metagenomics: more samples, more species, more MAGs
Learn how to cost-effectively level up your metagenomics research from expert bioinformaticians. PacBio HiFi sequencing is setting a new standard for quality and resolution in metagenome sequencing thanks to significant…
Unlocking the Genome with Long-Read Sequencing in Genetic Disease Research
Follow two scientists on their journey of discovery using whole genome sequencing and single-cell RNA sequencing to shed light on previously unresolved medical mysteries. In this video, they share how…
SFAF NGS Tech Panel (Teaser 2)
The COVID-19 pandemic has brought new focus and resources to pathogen surveillance of all kinds. HiFi sequencing, which combines high accuracy, long read lengths, and single-molecule sequencing, is unique in…
Computational Advances in Genome and Transcriptome Using HiFi Sequencing
PacBio HiFi sequencing has been used to generate the latest and most complete version of the human genome, characterize population-level structural variations, diplotype pharmacogenetic loci, and elucidate complex alternative splicing at the…
PacBio HiFiViral SARS-CoV-2 Kit
We created the HiFiViral SARS-CoV-2 Kit for labs working on the front line of the COVID-19 pandemic — tracking and identifying the spread of novel variants in their communities. The…
Scalable RNA Isoform Sequencing using Intramolecular Multiplexed cDNAs
While RNA-sequencing has dramatically accelerated our understanding of biology, quantitation and discovery of full-length RNA isoforms resulting from alternative splicing remain poorly resolved. Alternative splicing is a core regulatory process…
Uncovering Neurological Disorders Through an Examination of VNTRs
Many neurological diseases result from expansion of unstable variable nucleotide tandem repeats (VNTRs) that influence gene transcription of neighboring genes. In this talk, Dr. Henne Holstege presents research that investigated…