Gregory T. Lucier
Analyst · Macquarie
Thanks, Carol, and thank you to everyone who is joining us today as we provide an overview of our fourth quarter and full year 2012 results and expectations for 2013. We started 2012 with a promise to our shareholders to grow our underlying business, invest in growth markets and regions, deliver on balanced capital deployment strategy and introduce innovative new products to serve our customers even better. Our performance during the year had its challenges, including the weakened macroeconomic environment that affected Life Sciences' industry globally, and uncertainty in NIH funding in the U.S., in particular. But our management team and employees remain focused and were able to deliver against the promises we made. We introduced game-changing products across all our business groups, expanded further into emerging markets, built the foundation for our Molecular Diagnostics business, and increased our global manufacturing footprint in China, Singapore and Europe, allowing us to be ever more cost competitive. Now let me turn to the results. For the full year, we delivered revenue and earnings per share growth for the 13th year in a row. Revenue increased 2.2% to $3.8 billion, and our operating margin expanded to 29.2%. Non-GAAP earnings per share increased 7% to $3.98, and our strong free cash flow totaled $662 million, enabling us to invest in growing our business and return $635 million to shareholders through share repurchases. We finished the year strong with fourth quarter revenue growth at 4.5%, excluding currency. This growth was driven principally by Ion Torrent and our Research Consumables and Bioproduction businesses. Non-GAAP EPS of $1.11 came within the guidance we'd provided and included absorbing a negative $0.03 impact related to the benefit of the 2012 federal R&D tax credit being pushed from Q4 into the first quarter of 2013. Additionally, we delivered results even though a large order on our Applied Science business moved out of Q4 into 2013. We have been very focused on driving our Consumables business even higher. Our mix of consumables and services is now 85% of our total revenue. In addition, 2012 is the first year where over half our revenue has been generated outside of the Americas, making us an increasingly global company. Finally, we have focused over the last 18 months on reducing our exposure to academia and government, which we have been able to reduce by 10%. While this is still an important customer base for us, given the leading edge science taking place in those end markets, we invest more heavily in expanding our footprint in the faster growing hospital and clinical end markets. We continued to gain momentum as we expand in the higher growth markets through a combination of strategic acquisitions, partnerships and internal development. During the quarter and into 2013, we made acquisitions in our Research Consumables and Applied Sciences businesses, where we are able to immediately leverage our broad distribution capability. In November, we acquired AMG, the developer of imaging systems for research microscopy and the manufacturer of our FLoid Cell Imaging Station. AMG has grown rapidly by successfully developing a complete portfolio of cell imaging products across a range of functionality and price points, which allows us to compete more effectively with established players in a financially constrained environment. With AMG, we are able to expand our product line of cell imaging instrumentation, while leveraging our own molecular Probes, dyes and reagents for a total workflow system. In January, we acquired BAC, a leader in protein purification products with a unique set of innovative and proprietary affinity ligands, which are molecules capable of binding with specific proteins and are typically attached to chromatography resins in a production scale bio purification process. Protein purification is a growing market and a logical adjacency to our existing bioprocess business. With this bolt-on acquisition, our Bioproduction business is now squarely positioned as the provider of end-to-end solutions that are widely utilized in the bioprocess workflow and can compete more fully across the protein purification markets. In January, we also announced we had entered into an exciting new partnership with Boston Children's Hospital to form Claritas Genomics. This new company, in which Life will be a part owner, will develop next generation genetic and genomics-based diagnostic testing solutions for pediatric and inherited diseases, by standardizing their work on the Ion Torrent technology, including proton, PGM and the related consumables. Life is providing capital and technical support to ensure our sequencers are optimized for the workflow that will be developed at Claritas Genomics. We're very excited to have established what we believe is an innovative and flexible structure we can duplicate, going forward, as we partner with select institutions to accelerate the adoption of genetic testing and pediatrics, and ultimately, in advancing Ion Torrent technology into Molecular Diagnostics. And during the quarter, we continued to execute on our development pipeline with 2 production introductions in our leading qPCR business. At ASHG, we announced the QuantStudio 3D digital PCR system, a scalable, chip-based instrument that features a simple workflow with minimal hands-on time. This bench top platform is disruptively priced at $30,000, enabling access to a broad community and will compete in a global market that is expected to grow to $250 million by 2016. We also announced the launch of our QuantStudio Dx real time PCR instrument, which is CE IVD marked for use in Europe, and represents a significant extension of Life's product offerings in the diagnostics arena. Molecular testing is the fastest-growing segment of the diagnostics market, and QuantStudio has unique features to meet the needs of this market, including passage and detection, gene detection, gene expression analysis, SNP genotyping, microRNA and high-resolution melt analysis. Through a partnership with Quidel and others, we will have a menu of infectious disease and oncology tests, CE IVD marked for the European and Asian markets, being launched throughout 2013, bringing a high value menu to market unregulated platforms such as QuantStudio Dx, allows us to further penetrate the clinical markets outside the U.S. and begin the democratization of our platforms. Early in 2012, we laid out a strategy to build out our Molecular Diagnostics offerings and assets with a vision to become the most relevant provider of high-value information to assist physicians in the management of complex diseases. Our first investments were building one of the strongest management teams in the industry, with expertise in this area to bolster our commercial and regulatory efforts. Second, we built the foundation for this business with the acquisitions of 3 companies: Navigenics, Pinpoint Genomics and Compendia, through which we now possess arguably the most robust bioinformatics and physician portal capabilities in the industry, which will enable commercialization of high-value cancer diagnostics. In a very short amount of time, we've been able to assemble capabilities in software and bioinformatics and launch our first lab-developed test, the Pervenio Lung Cancer test service. Additionally, we now have a CLIA lab in one of our largest annotated databases of cancer patient samples globally. In 2013, and over the next several years, we intend to focus our efforts on strengthening our position in oncology and transplant diagnostics by developing a rich menu of compelling assays and panels on multiple platforms. As well, we plan to continue to create strong partnerships with leaders in these disease areas and work to build out our molecular diagnostic capabilities, largely through self funding initiatives. We believe we are well-positioned to deliver a continuum of systems to improve community access to information that will improve patient outcomes and reduce the overall cost of care. New introductions continued and continue the momentum of our installed base that allowed us to more than double the revenue of our Ion Torrent franchise for the second consecutive year. The fast-growing desktop market is highly competitive, and we estimate that our market share is now about 60%. We see this as the largest growth segment in the clinical research area of Molecular Diagnostics and look for Proton to grow that market share even further now. During the fourth quarter, we continue to launch new products that enhance our next generation sequencing offerings. We launched the new 400-base pair sequencing kit for the Ion PGM Sequencer, which produces reads 60% longer than comparable high-throughput benchtop sequencers, generating more complete bacterial de novo assemblies with longer contiguous sequences. We also made progress in expanding our best-in-class Ion AmpliSeq Panels. These panels allow our customers to do fast and affordable targeted sequencing for genes or genomic regions, and provide the highest level multiplexing with 3,000 targets per reaction, while requiring very small amounts of DNA, much less than other competitors, which is critical in research, especially related to cancer. We've already seen thousands of customer designs in the first 9 months of our custom AmpliSeq Panels. And with our new AmpliSeq Community Panels, we are rapidly growing panel menu across cancer and inherited disease, which is increasingly being utilized for clinical research. Last quarter, we launched our Ion Proton System instrument, a platform whose speed, ease-of-use and affordability will democratize genome sequencing by opening up the market to affordable clinical exomes and genomes. We are extremely pleased with the high level of customer interest. One full quarter into the launch, I'm pleased to say that we had our strongest quarter ever for Ion Torrent franchise, as continued strong demand to the PGM and a substantial sequential increase in the proton systems fueled our growth. We are seeing the real uptick of this technology as customers see how we have increased throughput, read-length and accuracy on the PGM and are confident we will be able to deliver it again on Proton. Proton with the P1 chip is the only bench top sequencer enabling human exome and transcriptome analysis today. With the PII chip, Proton will enable whole genome analysis. During the quarter, our businesses continue to generate strong free cash flow of $173 million. At the beginning of the year, we communicated our commitment to return 50% of our available free cash flow to shareholders. We ended the year having purchased $635 million, or 14 million shares in total for the year, well above that 50% level. We have continued to repurchase shares and have completed another $105 million to date in 2013 already. We have an additional $470 million remaining under a $750 million share repurchase program. As we move into 2013, we're focused on 3 priorities we believe will help us drive our performance and increase shareholder value. These include: Transforming our relationships with Life Science customers, meaning we're committed to providing our lab customers with the broadest array of tools and solutions, including web channels and sophisticated supply centers, so they can get their work done faster, more easy and less expensively. We think this will expand our market share. Second, we're focused on winning in Genetic Analysis from discovery to diagnostics, where we have platforms and expertise to move further towards clinical use; and finally, we continue to pursue growth in our applied markets, where we can apply our expertise and innovation to new opportunities to expand a current business or enter a new vertical in a very disciplined way. Moving on to guidance. We're expecting revenue growth of 3% to 5% over 2012 results of $3.8 billion, driven by another significant increase in our Ion Torrent franchise sales for the third consecutive year and expansion in our applied and emerging markets. Additionally, we expect to gain momentum from the roll off of a portion of the headwinds we had in 2012. The low end of the range, 3% growth, already assumes sequestration could reduce our revenue by approximately 1%, if implemented. While the fiscal cliff reduces the sequesters threatened NIH cut from 8.2% to 5.1%, there is now meaningful risk sequester will occur, at least temporarily. We therefore believe it's prudent to take a conservative approach here and revise as events unfold. For non-GAAP EPS, we're expecting results in the range of $4.30 to $4.45, applying 8% to 12% growth over 2012 results. We continue to do our best to navigate through these uncertain times, and remain committed to driving innovation and further diversifying our end market exposure. We are continuing to make investments in markets where we believe we have growth opportunities, such as next generation sequencing and Molecular Diagnostics that will make us increasingly more competitive and diversified. As we look ahead to 2013 and into 2014, we think many of these challenges to growing our top line have improved, and that through disciplined capital deployment we can grow our bottom line, while still making the necessary investments to be even more competitive over the next 3 to 5 years. Before I turn the call over to David, I would like to briefly address our annual strategic review. As you know, we recently issued a press release announcing that our Board of Directors had engaged outside financial advisors to assist them. While we normally would not have announced this, we believed it was prudent in light of speculation in the media. The Board's annual review started last summer, when our stock was trading in the low 40s. The Board engaged financial advisors to help in valuation work and reviewing opportunity to create value for our shareholders. As any thorough review would entail, all ideas are on the table, including pursuing our current strategy, which has yielded solid results, or something different. The Board has not decided on any specific course of action, but any decision will be based on what the Board believes is in the best interest of shareowners to further create value. I recognize that many of you have many questions on this topic. At this time, I am unable to comment further or provide any additional information. The Board's review is ongoing, and we will update you as appropriate. In the meanwhile, the more than 10,000 Lifetech employees around the world remain totally focused on our customers and making 2013 another great year. With that, I'll turn the call over to David.