In this virtual symposium, hear from a variety of researchers who are using the PacBio Iso-Seq method for bulk and single-cell transcriptomics to drive cutting-edge research in neurology, neurodegenerative diseases,…
In this webinar Zhongxiao Li will discuss: • Building the first isoform-resolution colorectal cancer (CRC) transcriptomic atlas • Characterizing genes and isoforms associated with different epithelial lineages and subpopulations •…
Detecting cancer-related RNA dysregulation with long-read sequencing Full-length, single-cell RNA data provides critical insights into the understanding of cancer transcriptomic features, such as isoforms, fusions, and expressed mutations. However, until recently, cell…
In human, non-human, and cancer genomic research, there is a pressing need for streamlined, efficient computational approaches that can reconstruct high-quality, chromosome-scale phased sequences at scale. In this webinar, Shilpa…
Large, diverse datasets are critical to ensuring that the promise of genomics can be realized by more people in more places around the world than ever before. Whether research is focused…
Full-length RNA data from single cells provides critical insights to better understand the intricacies of cancer transcriptomics. Find out from Arthur Dondi how he uses a high-throughput PacBio sequencing approach…
Dr. Nathan Salomonis of Cincinnati Children’s Hospital Medical Center presented how he used the MAS-Seq kit and sequencing on the PacBio Revio system to provide new insights into leukemia clonal…
Con este seminario web descubrirá como las secuencias largas y de alta precisión le ayudarán a lograr nuevos descubrimientos en sus investigaciones, y cómo el nuevo sistema Revio está revolucionado…
Leading scientists from PacBio and Zymo Research will present state-of-the art HiFi metagenomic sequencing solutions that will enable microbiome researchers to make important discoveries
Variable number tandem repeats (VNTRs) make up almost 3% of the human genome and are difficult to map, due to their repetitive nature. In this webinar, Mark Chaisson, PhD, of…
Effective carrier and newborn screening methods are critical for solving problems in reproductive medicine and launching treatment plans for early-onset genetic diseases. Clinical research faces a number of well-known challenges…
Join us for an engaging webinar where PacBio scientists will present the MAS-Seq method, an all-new kitted single-cell transcriptomics solution that delivers exceptional data quality and explanatory power for your next big breakthrough…
Find out how to generate and analyze full-length adeno-associated virus (AAV) sequencing data to profile packaged genomes as a single intact molecule, measure impurities, and ensure vectors contain the intended…
Do you need to detect epigenetic modifications in native DNA, even in difficult regions? Then join us virtually for the first webinar in our new bioinformatics series. In this webinar…
Hear about new tools in human genomics research that will help you do more and further your discoveries. Our speakers will discuss the capabilities of a new PacBio solution –…
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