Join PacBio’s Mike Weiand to hear how gene editing protocols can benefit from long-read sequencing at multiple stages to optimize and enhance vector integrity. This method allows researchers to reveal…
With highly accurate long reads (HiFi reads) of >99% accuracy, the Sequel IIe System is the tool of choice for producing reference quality assemblies, calling variants with the highest precision,…
The Sequel IIe System produces highly accurate long reads (HiFi reads) quickly and cost-effectively thanks to increased computational capacity and on-instrument data processing. This results in a significant reduction of…
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…
In this webinar, hear from Jeanette Gehrig, Ph.D., Senior Scientist at Siolta Therapeutics, about how her team is leveraging PacBio metagenomic sequencing to achieve: (1) Strain-level resolution of bacteria from…
In this BioConference Live webinar, PacBio CSO Jonas Korlach highlights how multi-kilobase reads from SMRT Sequencing can resolve many of the previously considered ‘difficult-to-sequence’ genomic regions. The long reads also…
Lizzie Wilbanks formerly from UC Davis, discusses how longs read from SMRT Sequencing allow accurate assembly of members from the complex pink berry salt marsh community.
In this webinar, the presenters describe a targeted sequencing workflow that combines Roche NimbleGen’s SeqCap EZ enrichment technology with PacBio’ SMRT Sequencing to provide a more comprehensive view of variants…
Brett Hannigan, Computational Biology Project Leader at DNAnexus, demonstrates a fast, accurate, and cost-efficient solution for diploid-aware de novo genome assembly utilizing FALCON on the DNAnexus platform.
Andrew Carroll, Director of Science at DNAnexus, presents how to greatly improve the accuracy of SV-calling by using long-read PacBio sequencing and fast and easy-to-run cloud-optimized apps like PBHoney, Parliament,…
This presentation describes a new genome browser for read alignments around complex variation: genomeribbon.com. Ribbon was built for viewing genomic read alignments around structural variants. It is very useful for…
PacBio Sequencing is characterized by very long sequence reads (averaging > 10,000 bases), lack of GC-bias, and high consensus accuracy. These features have allowed the method to provide a new…
Tetsuo Ashizawa, Director of the Neuroscience Research Program at Houston Methodist Research Institute, presents a novel amplification-free targeted enrichment method using CRISPR-Cas9 for the disease-causing repeat expansion in SCA10. Using…
Meredith Ashby, from PacBio, presents how large-insert targeted sequencing (LITS) provides a more comprehensive picture of structural variation relevant to human disease and genomic disorders, providing insights into possible rearrangement…
Melissa Laird Smith from Icahn Institute at Mt. Sinai reviews her work studying the genetic background of immune response by characterizing population diversity at the immunoglobulin heavy chain locus. Webinar…
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