Christian Henry
Analyst · Canaccord. Please go ahead
Thank you, Todd. Good afternoon and welcome to our fourth quarter results and business highlights call. Thanks for joining us today. We have a lot of exciting news to share and I'll kick things off with an update on our performance in the fourth quarter and 2022, I'll then delve into some exciting developments we've seen in the past few months and wrap up with an update on our market segmentation. Susan will then provide a more in-depth look at our financial results and our guidance. But first, a quick recap on revenue. Our most transformative long-read sequencer today, we are just a few weeks away from broad commercial availability of Revio, which is scheduled for next month. Currently, we have dozens of instruments on the manufacturing floor in our Menlo Park facility. And at this point, we don't see any serious supply chain constraints. As a result, I expect that we'll ship at least 25 Revio systems to customers prior to the end of the quarter. We will continue our manufacturing scale up through the second quarter and I believe we will be at our planned production rate for 2023 by the end of Q2. This is good news as the Ravio platform enables our customers to take on projects in the thousands to tens of thousands of samples. With this scale, we believe Revio will be a game changer for scientists and clinical researchers. What would have taken years or even decades with long-read sequencing in the past can now be completed in a fraction of the time and cost with the Revio platform. For years, the scientific community has relied on short-read genomes and exomes, yielding valuable insights into the human genome. However, despite millions of short-read genomes being sequenced, much of the genome remains unactionable today, and our understanding of our 20,000 plus genes and their role in driving disease is still quite limited. Further, we now know that phenotype is not solely determined by genes, as mutations in non-coding regions can cause certain cancers. Our understanding of the impact of methylation on genetic disease is in its earliest stages. And we also recognize that the importance of both sequence length and accuracy in understanding disorders caused by tandem repeat expansions. It’s clear that to better understand the human genome researchers must be able to interrogate its full complexity with high accuracy. We expect that sequencing with the Revio platform will provide researchers with the most complete and accurate view of the genome in a single assay. With Revio, researchers will be able to interrogate the genome from telomere to telomere, obtained phasing information, structural variation, epigenetic profiles, and of course, single nucleotide variants, all at the scale and affordability required for large projects. The early excitement around Revio and the immense possibility for genomic support our belief that we can grow our revenue towards our goal of a compound annual growth rate of 40% to 50% through 2026. As we work to achieve our revenue growth targets, we see 2023 as a year of product transition. We expect many Sequel II and IIe users will migrate over to Revio over the course of the year. These transitions are difficult to precisely predict and as a result, we may see some temporary variability with respect to consumable revenue. On the instrument side of our business, we expect to see continued strength for Revio throughout the year. Additionally, we do expect to place a modest number of Sequel IIe systems and of course, also our short-read sequencer remains on track for commercial shipment in Q2 of 2023. As a result, our initial guidance for 2023 is that we expect to achieve between 165 million to 180 million in revenue, which represents growth from 29% to 40%. Now, turning to our results. In the fourth quarter, PacBio achieved revenue of $27.4 million, a 24% decrease compared to the previous year's quarter. The decline in revenue was primarily driven by the announcement of the launch of revenue in the fourth quarter, which impacted orders and shipments for Sequel IIe. We delivered 18 Sequel IIes systems during the fourth quarter, bringing our total installed base to 512 Sequel II and Sequel IIe systems as of December 31. However, what truly sets this past quarter apart is that we received orders for 76 Revio systems, a record-breaking start for a PacBio launch and far surpassing our expectations. We have seen a growing excitement around the potential of Revio as indicated by the positive feedback we have received from our customers. At the recent AGBT Conference, many customers told us how Revio could help them scale their research and interrogate the genome at unprecedented levels. At the Plant & Genome Conference in January, we saw a deep appreciation for the importance of HiFi sequencing and the enthusiasm for higher output long read sequencing in the community. We hosted a packed workshop where researchers from Corteva, UCLA, and HudsonAlpha discussed how PacBio sequencing advances their work in agri genomics, biodiversity, and plant evolution. We are thrilled to announce that the first early access Revio is in route to researchers at the Broad Institute. Over the next few weeks, the team at the Broad Institute will perform their first internal sequencing runs on the platform, and in March, we expect to begin full commercial shipments. The Broad has already ordered 10 Revio systems to scale long read sequencing for programs like the NIH's All of Us program. To put that in perspective, 10 Revio systems has the equivalent sequencing power of 150 Sequel IIes. We look forward to supporting this project and more population scale research initiatives to come. While on the topic of All of Us, I wanted to discuss a recent preprint for researchers involved in the program which highlights the utility of long read sequencing. The authors noted that HiFi reads produced the most accurate results for both small and large variants, and concluded that "long reads have widespread value for generating complete and accurate variant call calls". The study also showed that PacBio is best-in-class for calling variants even at lower coverage than other technologies. This supports our belief that even a PacBio genome at 10-fold coverage can be more than sufficient for many research projects. At 10-fold coverage, a Revio can sequence 12 human genomes in 24 hours, or almost 4,000 genomes per year at a list price of approximately $330 per genome with methylation included. The demand for highly accurate reads is increasing as evidenced by the recognition of long read sequencing has nature methods, method of the year with innovative studies utilizing PacBio's long reads from the Vertebrate Genome Project Telomere American Consortium and the Human Pan Genome Reference Consortium, we believe Revio can drive further discovery with its enhanced throughput and cost effectiveness. Our existing customers have also recognized the potential of Revio to accelerate their research. For example, Mohammed Bin Rashid University Of Medicine and Health Sciences, or MBRU purchased Sequel IIe last year and ordered multiple Revios in the fourth quarter to sequence for a very large scale research project in Dubai. And the Wellcome Sanger Institute, a longtime user of PacBio for plant and animal research now plans to increase its use of long-reads in human applications, such as single cell transcriptomics and variant detection with the added power of Revio. Moving on to Onso, our beta program is in full swing at the Broad Institute, Corteva Agriscience, and Weill Cornell, each evaluating how Onso’s extraordinary accuracy can benefit their various genomic applications. Feedback so far has been excellent, with one partner sharing that they've been extremely impressed by Onso’s levels of accuracy and another thing how highly accurate reads will be transformative for many genomic applications, including oncology. We're pleased to announce that we're on scheduled to begin commercialization of Onso in the second quarter, with a launch specification of 400 to 500 million reads and 200 cycle and 300 cycle kits. The expected specification for accuracy of over 90% of the bases at Q40 Plus and the potential to reach Q50 Plus through approved library preparation we believe Onso will set a new standard in the industry. The system has a competitive list price of 259,000 with the 300 cycle kit listed at $1,995. We're collaborating with workflow partners across the short-read ecosystem and will provide library prep conversion kits, so that any current short-read assay can move directly onto the Onso platform. Regarding its capabilities, we have validated Onso’s performance through various testing methods, including the SAR-Seq cell-free DNA control with Agilent library prep and capture and our conversion kit. Internal results demonstrate that Onso is two times more sensitive in detecting variant allele frequency of 0.5% and is 1.4 times higher sensitivity even when applying duplex [indiscernible] at four times the coverage with other short-read sequencing technologies. These performance metrics highlight the exceptional value that Onso can bring to the market, offering high accuracy and sensitivity to meet the demands of various genomic applications, including cell-free DNA research. In addition to cell-free DNA in collaboration with 10x genomics Onso achieved 99.8% of the bases at Q30 or better for single-cell RNA reads showing the potential use of ultra high accuracy in single-cell workflows. We are dedicated to providing our customers with comprehensive and streamlined solutions for their sequencing workflows. This includes offering a range of tools and workflows that are designed to support their success, from automation to sample preparation and informatics. Our recent initiatives include expanding our MAS-Seq program to support new assays on the Sequel II and IIe and Revio sequencing systems. These kits which build on the success of last year's MAS-Seq concatenation technology for single-cell isoform sequencing includes 16S and bulk Iso-Seq and will be available later this year. Additionally, our bioinformatics team is continuously improving interpretation tools, such as the recently launched paraphrase tool that helps characterize the dark regions of the genome linked to spinal muscular atrophy. On top of our internally developed products and tools, we're partnering throughout the ecosystem to make it more plug and play. As such, we recently introduced the PacBio compatible program designed to make PacBio sequencing more accessible, which includes partners across all ends of the sequencing workflow, from automation and sample and library prep, to secondary and tertiary analysis tools. Moving on, I want to share an update on our internal market segmentation from the previous year. In 2022, human genomics was the largest portion of our business, accounting for nearly 40% of our revenue. Customers in this segment include GenDx, who recently ordered a Revio to target difficult to sequence genes and sequence human whole genomes for rare diseases, with previously inconclusive results. In Radford University has leveraged PacBio technology to make numerous genetic discoveries and plans to ramp-up from hundreds to thousands of genomes using Revio. Beyond human applications, we expect Revio to be utilized in applied markets like plant and animal genomics, which made up about 25% of our revenue in 2022. In this market customers like Corteva Agriscience are utilizing PacBio to study plant genomes and identify microbial infectious diseases that affect these plants, so they can improve crop yields and drive agricultural sustainability. Plant and animal genomics also include research programs like the Darwin Tree of Life Project, which recently celebrated sequencing its 500 HiFi genome. The program aims to sequence 70,000 species of eukaryotic organisms in Britain and Ireland, and we expect Revio to enable the researchers to progress towards this goal. Additionally, infectious disease and microbiology, which represented 20% of our revenue in 2022 includes customers like Bioengineering Lab, who plans to use Ravio for metagenomics to discover and characterize communities of microbes for industrial and biomedical applications. About 10% of our 2022 revenue was from oncology applications, with PacBio’s highly accurate long reads, allowing researchers to uncover novel isoforms, fusions and structural variants with exceptional accuracy. Looking ahead, we expect to address more of this large market with Onso's potential for extraordinary sensitivity in liquid biopsy applications. The remaining portion of our revenue comes from other and emerging applications. This includes gene editing and gene therapy applications. Finally, we are pleased with the support and interest from investors in our equity raise last month. In an upsized offering, we raised $201 million in gross proceeds, which will further bolster our ability to grow our business and drive towards our goal of positive cash flows during 2026. With that, I'd like to turn the call over to Susan to discuss our financials and guidance in more detail. Susan?