Good afternoon, ladies and gentlemen, and welcome to Veracyte's third quarter 2021 financial results conference call. As a reminder, today's conference call is being recorded. I'd now like to turn the conference over to Tracy Morris, Veracyte's Vice President of Corporate Communications and Investor Relations. You may begin. Thank you, Erica. Good afternoon, everyone, and thanks for joining us today for a discussion of our third quarter 2021 financial results. With me today are Marc Stapley, Veracyte's Chief Executive Officer, and Rebecca Chambers, our Chief Financial Officer. Veracyte issued a press release earlier this afternoon detailing our third quarter financial results. This news release, along with the business and financial presentation, is available in the Investor Relations section of our website at veracyte.com. Before we begin, I'd like to remind you that various statements that we may make during this call will include forward-looking statements as defined under applicable securities laws. Forward-looking statements are subject to risks and uncertainties, and the company can give no assurance that they will prove to be correct. Further, we are not under any obligation to provide further updates on our business trends or our performance during the quarter. To better understand the risks and uncertainties that could cause actual results to differ, we refer you to the documents that Veracyte filed with the Securities and Exchange Commission, including Veracyte's most recent Forms 10-Q and 10-K. I will now turn the call over to Marc Stapley, Veracyte's CEO. Thanks, Tracy, and thanks everyone for joining us today. It's a pleasure to be here to provide an update. We are pleased with our performance in the third quarter as we delivered revenue of $60.4 million, representing growth of 94% over the prior year, despite some COVID-19 related headwinds. We have also executed on some key milestones since our last update, significantly advancing our strategy. In August, we completed the acquisition of HalioDx, securing our future to develop and manufacture our own test kits for the nCounter system. This will provide physicians and their patients all around the world with access to our growing menu of tests, which we are in the process of transitioning to the instrument. Prior to considering the transfer of our tests onto the nCounter, they're developed as LDTs for the U.S. market in one of our CLIA labs. We pursue reimbursement via a process of evidence development, publications, guideline inclusion, and KOL adoption. Our tests are designed from the ground up to answer very specific clinical unmet needs while fitting into the physician's workflow, and they leverage not only our deep scientific expertise in whole transcriptome genomics, but also now our expertise in immuno-oncology, a rapidly growing field. With the addition of HalioDx, we now address eight of the top ten cancers in the U.S. by indication. Our expanding menu of tests will improve outcomes for patients all over the world at every step of their journey by, for example, ruling out unnecessary surgeries, providing diagnostic clarity, helping physicians with treatment decisions, or helping to detect cancer early when it can be successfully treated. To further assist physicians with the treatment of patients, our menu of tests is bolstered by our partnerships with biopharma companies to whom we provide our extensive genomic and clinical data and services to assist in the development of therapies and companion diagnostics. Turning now to the quarterly results. As always, I'll discuss our progress in the context of our strategic drivers of commercial growth, evidence development, pipeline advancement, and global expansion. Beginning with commercial growth. The Decipher Prostate Genomic Classifier continued to gain strong traction in the market, further fueled by ongoing sales team expansion. You will recall that our prostate cancer business is less impacted by COVID-19 because many of our urologist customers practice in community settings as opposed to hospitals, and community settings in general have been more accessible to patients and our sales reps. We expanded coverage for Decipher Prostate, making the test a covered benefit for an additional five million plan participants and bringing the total number of covered lives to more than 150 million people nationally in the U.S. We also signed a new contract with a large Blues plan and a national government payer. In September, the National Comprehensive Cancer Network, or NCCN, published its 2022 guidelines, which specifically recommend treatment decisions based upon the patient's Decipher Post Radical Prostatectomy, or RP, score. Ours is the only genomic prostate cancer test with this level of recommendation, which we believe will help to further drive adoption and reimbursement. Our Afirma Genomic Sequencing Classifier, or GSC, continues to be the new standard of care in thyroid cancer diagnosis. Afirma GSC revenue and volume increased over prior year, although both were slightly down sequentially as we experienced summer seasonality with higher than typical rates of vacations, hospital staffing shortages, and challenges from the COVID-19 Delta variant. Approximately 70% of our Afirma samples come from procedures performed in a hospital setting, which have tended to be more impacted by COVID, limiting biopsy procedures and sales rep access, particularly in those areas where the case count and hospitalizations have been high. We're also pleased to welcome Dr. Joshua Klopper as our new Medical Director for Endocrinology. Dr. Klopper was an investigator on our original clinical utility study for the Afirma test, and he will play a key role in further establishing the test as standard of care and guiding our ongoing market development work in thyroid cancer. Our pulmonology business continued to be impacted by COVID, as we saw in prior quarters. This stems from the ongoing reduction in the number of bronchoscopies, the procedure used to collect samples for both our Percepta GSC and Envisia tests. Despite limited access, we continue to build awareness of our pulmonology products by leveraging digital marketing to educate our customers and targets with KOL-led online educational events, peer-to-peer engagement tools, and other digital communications. Our Prosigna breast cancer business gained momentum in Europe, where our ability to report molecular subtype information and enable laboratories to perform the test locally gives us key competitive advantages. Our next strategic growth driver is evidence development. We further boosted our library of clinical evidence across our urologic cancer, pulmonology, and endocrinology products with two published studies and six abstracts of major medical conferences, which we believe will help facilitate adoption and reimbursement for our tests. At the CHEST Annual Meeting in October, we unveiled expanded clinical validation data for our Percepta Nasal Swab, which further reinforced the test's ability to help physicians assess lung cancer risk in patients with lung nodules. The findings also showed that our test delivers strong clinical performance across different nodule sizes and cancer stages, and for patients who have already had other cancers. Importantly, the data showed that when nasal swab identifies patients as low risk for cancer, its sensitivity was very high, 97%, meaning that it will miss very few cancers. Conversely, when the test identifies patients as high risk for cancer, its specificity was also high, 92%, meaning that it can help ensure that patients who are more likely to have lung cancer can be quickly guided to further diagnostic procedures and treatments if needed. Also, at the CHEST meeting, researchers shared results of a new decision impact study for Envisia for interstitial lung disease, including idiopathic pulmonary fibrosis or IPF. The findings showed that use of the test increased physician diagnosis of IPF and that when they did diagnose the disease, they were more confident in their decision and also more likely to initiate IPF therapy. Accurate, timely diagnosis is important for IPF patients because it can enable them to begin treatment with antifibrotics that can slow progression of their disease. Further, data shows that immunosuppressive agents, which are frequently used to treat many interstitial lung diseases, can actually be harmful to patients with IPF. Data from two important studies for our prostate test were shared at the American Society for Radiation Oncology, or ASTRO, annual meeting in October. The first study, which examined our Decipher Prostate test, was the first to validate the use of any genomic test in a prospective randomized cohort of prostate cancer patients with long-term follow-up. In this case, a median of 11 years. Results demonstrated that Decipher Prostate test scores are independently associated with distant metastases, prostate cancer-specific mortality, and overall survival in patients with clinically high-risk prostate cancer. The findings suggest that use of the test can help identify patients who may require treatment intensification beyond standard of care therapy. Additionally, findings from a multicenter randomized phase III trial presented at ASTRO suggest that the Decipher Prostate-RP test can guide timing and intensity of treatment for men experiencing prostate cancer progression following surgery. For the Decipher Bladder test, our tool that helps physicians manage treatment decisions for patients with bladder cancer, new data were published in the Journal of Urology showing that the test accurately identified patients whose bladder tumors were most likely to respond to chemotherapy prior to radical cystectomy. These findings suggest that the test could ultimately help physicians optimize treatment planning for their patients with bladder cancer based upon their tumor subtype biology. Until now, there has been no reliable way for physicians to distinguish these cancer types, resulting in overuse of neoadjuvant chemotherapy with little benefit for many patients. Additionally, results of a long-term clinical utility study for the Afirma GSC were published in the Journal of the Endocrine Society. These findings showed that use of the Afirma GSC resulted in 41% fewer surgeries among patients whose thyroid nodule fine needle aspiration results were indeterminate compared to patients who had no molecular testing. Additionally, when surgery was performed, patients deemed suspicious for cancer by the Afirma GSC were nearly twice as likely to have cancer compared to those who had no molecular testing. Turning to pipeline advancement, which is our third strategic growth driver, we have recently achieved a number of key milestones. We were delighted to launch our Percepta Nasal Swab test for early lung cancer risk assessment in October. We believe the clinical need for this test is significant because physicians today lack objective, accurate tools to determine which patients with lung nodules are likely benign and can therefore avoid unnecessary diagnostic procedures, and which patients likely have cancer and should be directed to further diagnostic workup and treatment if needed. With 15 million Americans currently eligible for annual lung cancer screening and 1.6 million lung nodules found incidentally, the ability to reliably determine next steps becomes increasingly important for patients, physicians, and the healthcare system. With the non-invasive Percepta Nasal Swab, we believe that more lung cancers will be detected early when they can be successfully treated. We are making the Percepta Nasal Swab test available to a limited number of sites as we assemble the clinical utility evidence to help secure reimbursement, working up to an initial 50 sites that we would plan to engage in our clinical utility study. Work on Percepta Genomic Atlas, our genomic profiling test for patients with confirmed lung cancer, is progressing. We now expect to launch the test in our CLIA lab in early 2022 and still anticipate 6-12 months post-launch to receive reimbursement. The test will round out our portfolio of three products serving the lung cancer patient from early detection to diagnosis and treatment. Another key product launch was our Decipher Bladder test. Our sales team has begun offering the test to our urology customers, the same physicians that we serve with our Decipher Prostate test. The launch will be steady and measured to ensure that we maximize the long-term potential of this test, which could help in the treatment of up to 80,000 patients a year without disrupting our growing prostate business. As I mentioned earlier, we completed our acquisition of HalioDx on August 2, marking a key step in our strategic plan for global expansion. I've been delighted to welcome the company's talented team to Veracyte and four of its leaders to my executive team, namely Vincent Fert as EVP of Immuno-Oncology and EU Operations, Stéphane Debono as SVP and General Manager of Immunoscore and International Diagnostic Operations, Corinne Danan as SVP and General Manager of our new Biopharma BU, and Fabienne Hermitte as SVP Global Quality and Regulatory Affairs. Our combined team is already collaborating on the move of our IVD test manufacturing from NanoString to our facility in France. This transition, which we estimate will take 24 months, will give us end-to-end control over our IVD product business. In parallel, we plan to port additional tests, including Envisia, Decipher Prostate, and the Percepta Nasal Swab to the nCounter analysis system, so that we can make them available to physicians and their patients in global markets. We have made great progress in finalizing the plans for these development projects, which will be an exciting collaboration between our experienced R&D teams in South San Francisco, San Diego, Marseille. I look forward to updating you on the timing in due course. The HalioDx acquisition also expands our scientific expertise into the emerging area of immuno-oncology, offering a range of products and services for clinicians and biopharma partners that leverage novel insights into the tumor microenvironment. The impressive Immunogram platform gives our biopharma partners a multimodal 360-degree biomarker analysis of the tumor sites, helping them to understand and predict patient response to immunotherapy with the potential to help further inform patient care from treatment decisions to risk of recurrence. Additionally, the acquisition has brought us the Immunoscore Colon Cancer test. This test is intended to guide treatment decision-making by giving physicians a clear and actionable measurement of how an individual patient's immune system is responding to their cancer. The integration has gone extremely well so far. I'd like to thank Bonnie and the work stream leaders and teams from both Veracyte and HalioDx, who have worked tirelessly to ensure that we accomplished our integration goals while maintaining a strong focus on the respective businesses. In summary, we had a strong quarter in which we delivered solid revenue growth year- over- year and positioned our tests for further physician adoption and reimbursement. We also made significant progress in transforming the company for long-term growth through the launches of key new products and through the successful acquisition of HalioDx to achieve our global strategic vision. I'll now turn the call over to Rebecca to give a detailed overview of our results. Thanks, Marc. As Marc mentioned, we are pleased with our third quarter performance. Our revenue for the quarter was $60.4 million, an increase of 94% over prior year, and included a $4.7 million revenue contribution from HalioDx. Our strong results were driven largely by outstanding commercial execution in our urology business. Testing revenue equaled $50.9 million with an ASP of approximately $2,700 per test. Afirma, Envisia, and Percepta GSC were over 11,000 tests in total, an increase of 10% compared to the third quarter of 2020, while Decipher contributed nearly 7,500 tests to the quarter. Product revenue contributed $3 million or 45% growth year- over- year with Prosigna volume of around 2,150 tests. Biopharmaceutical and other revenue equaled $6.5 million, including HalioDx. Testing gross margin was 68%, and our product gross margin was 50%, both of which were slightly lower sequentially. Biopharmaceutical and other gross margin was 37%, lower sequentially, primarily due to a purchase price accounting adjustment to the inventory held by HalioDx. In total, gross margin was 64%, a decrease of 400 basis points sequentially. Operating expenses, excluding the cost of revenue, increased $10.3 million sequentially to $55.4 million. Of the sequential increase, $7.5 million was related to stock-based compensation expense, intangible asset amortization, and acquisition costs attributable to the HalioDx acquisition. Broken down by category, the $55.4 million of operating expenses are as follows. R&D expense grew $1.8 million to $8 million, driven primarily by the two-month impact of the HalioDx R&D organization. Sales and marketing expenses grew $2 million to approximately $21.7 million, again, driven primarily by the two-month impact of HalioDx. G&A expenses were $20.7 million, including approximately $5.8 million of acquisition-related expenses. Total operating expense included $8 million of stock-based compensation expense. We recorded a net loss of $14.1 million, including $6.3 million of net loss from HalioDx and $5.8 million of acquisition-related expenses. Net cash used in operating activities was $1.4 million, and we ended the quarter with $168 million of cash equivalents, and short-term investments. Turning now to our 2021 guidance. Given the potential for volatility created by vaccine mandates, staff shortages, COVID, and supply chain challenges, we are maintaining our previous guidance range while adding the contribution from HalioDx. As a result, we are now projecting revenue of $210 million-$218 million, including HalioDx revenue of approximately $10 million. In all, we are pleased with the quarter and remain confident in our position and ability to execute on our plans as we build on our success through 2021 and beyond. Thank you for your time. I will now turn the call back to Tracy. Thank you, Rebecca. We will now go into the Q&A section of the call, and joining us will also be Dr. Giulia Kennedy, Veracyte's Chief Scientific Officer and Chief Medical Officer, and Dr. Tina Nova, General Manager of Thyroid and Urologic Cancers. Operator, please open the line. The floor is now open for questions. At this time, I would like to inform everyone in order to ask a question, please press star one on your telephone. We'll pause for just a moment to compile the Q&A roster. Your first question comes from the line of Puneet Souda from SVB Leerink. Your line is open. Yeah. Hi, Marc, Rebecca, thanks for taking the question. First one is really on the guide. I just wanna clarify the $10 million contribution from HalioDx. When the acquisition happened, if I recall correctly, it's growing at a clip of about 25% or so. Just wondering if that is what you're contemplating this year or if there is any change from that in the fourth quarter. Then if we look out to 2022, is there any difference versus that prior expectation? Yeah, thanks, Puneet. Appreciate the question on that. You know, if you do the math, we had HalioDx in our numbers for essentially two months of the quarter in Q3, and our guide for Q4 contemplates a couple of things. Firstly, it contemplates you know, the same kind of volatility that we and others are seeing around the quarter in general related to COVID first and second order effects, you know, effects on you know, due to Delta variant, for example, on the supply chain potentially and on staffing shortages and other. That's one element. The other is you know, while the integration is going exceptionally well, I have to say, you know, I've done and been involved in many acquisitions in the past and they always have some distraction for the business. We've been able to ride that fairly well so far, but I wanna make sure in our guidance we give ourselves a little bit of room for that. Then kind of more specific on that point, you know, one of the things that the Halio team or the Marseille team is very focused on right now is working across with our R&D teams in San Diego and South San Francisco to develop our products for the nCounter platform. That's the same team that carries out, you know, third-party IVD work. You know, while that team is able to juggle those different things, again, I wanna make sure we've got room in our forecasts for that. Bear in mind and remember, we acquired HalioDx primarily for the manufacturing capability, and so that is our priority number one is that transition. Meanwhile, in addition to that, we got some fantastic assets in the IVD services business and the biopharma business and the Immunogram platform and Immunoscore. You know, we're gonna benefit from those over the longer term, but right now, short-term priority is manufacturing transition to that. The only thing I'd add to that, Puneet, is that does extend into 2022 per Marc's comments. Our priority will be the bio business as well as the manufacturing of contract manufacturing for IVD. Okay. Great. In terms of, I think you alluded to this somewhat, earlier in terms of the sluggishness that you're seeing obviously impacted on Afirma and more Percepta as well, with hospital access. Maybe just could you remind us where you stand today, right here in November in terms of the rep access? What are you seeing in terms of both the thyroid in-person sales reps and the prostate in-person sales reps and any indication that that is, you know, on a steady improvement versus, let's say, September or so? Yeah. I mean, parsing it out and you know what I will say is there's a lot of kind of volatility here business by business or month by month. Let me go through it. I'd say timing-wise, you know, we did see particularly a greater effect than we anticipated in the middle of the quarter. Things definitely improved towards the end of the quarter, but October's you know gotten off to a start that's more similar to the beginning of the quarter than the end so far. If you go business by business, though, you know, we continue to see across the pulmonology business, which is the most impacted, problems with access and reduced number of procedures. Again, these are hospital-based settings, 70% or so. You really do. In fact more than that, you really do see an impact in pulmonology. That's not gotten better recently, and we're not anticipating much change there going forward right now. Afirma did get impacted, and we talked about that and anticipated that might be the case because Afirma itself is 70% or so in the hospital setting. Then in those areas that were particularly impacted by COVID Delta regionally, we did see the most impact on both sales rep access and patient reticence and, you know, procedures. We also saw an impact in staffing shortages, which are across the board, but you know, we definitely saw that happen in Afirma. That's more general to the hospitals and that's one thing that we think could continue and might be exacerbated by, you know, vaccine mandates and so on. One of the things we remain cautious about is the staffing situation at our customers. Then moving to Decipher. Decipher's been particularly resilient during COVID to kind of case counts and so far to most geographic impacts. I mean, there's not zero impact, but it's relatively, you know, negligible when you look at the growth of the business. It is a growing business. However, I think staffing shortages would be something to watch for that business as well going forward. Yeah, we're continuing to remain cautious about that. Rebecca, anything you wanna add? No, thank you. Okay. You covered it. Got it. Just last one, if I could squeeze one on nasal swab. That's obviously an important product for you. Just as you stand today, given the early work you're doing with the sites, could you just remind us what sort of reimbursement that we should imagine for this product? In terms of the you know data sets, do you have enough data at this point to move forward with the reimbursement or the clinical utility that you're working on with these early sites is gonna be in you know included into that for the reimbursement? Thank you. Thanks for taking my questions. Thanks, I appreciate it. That yeah, really important product. You know, nasal swab is incredible progress. Again, as I mentioned this quarter, you know, we launched the product at limited sites, and we're continuing to grow those sites. Now in terms of the data, you know, we announced new data this quarter that enhanced the clinical validity data of the test, and you know, we can spend more time on that if people want to. You know, in terms of clinical validity, we've got some fantastic data for the nasal swab. The next step is the clinical utility data through those sites, and that's gonna take time. We wanna pick the right sites, and we wanna get this done the right way and done properly to secure the long-term prospects for this breakthrough product. We wanna make sure that it's launched in the best possible way. We're in the process now of doing that. We'll gather the data. We still think reimbursement could be fairly broad range from 12-24 months till we get to that point. The most important focus right now is building that clinical utility data and going through the reimbursement process, something which Veracyte has had incredible experience and an exceptional track record of doing extremely well. We're leveraging our experience there. Great. Thanks, guys. Thank you. Your next question comes from the line of Tejas Savant from Morgan Stanley. Your line is open. Hi, this is Yuko on for Tejas. Thank you for taking our questions. Would you comment on whether you're seeing any pressure on the supply chain now? What are some of the actions that you're taking to ensure there are no risk disruptions? Yeah. I mean, the supply chain pressure. Lots of people are talking about it, and it's very real for many. Throughout COVID actually, we've been able to ride that out very well with our suppliers. You know, we've made a concerted effort to talk to many of our large suppliers and see what they're seeing and hearing right now because you know, one thing you do have to worry about is the second and third order effects on them and their suppliers. So far so good. Doesn't mean that, you know, things couldn't happen, but so far we haven't had too many problems. You know, every now and then there's issues, but we're able to resolve them fairly quickly with our vendors and partners, who collectively I think are doing an exceptional job of managing through this. Again, we're remaining cautious about it. It's very real. It could happen, and we're watching it closely and, you know, to some extent are anticipating the odd road, you know, speed bump here and there, but so far nothing major to report. Great. And then would you provide an update on the rollout of nasal swab and the number of sites where you have rolled it out so far? What's been the early feedback on the classifier so far? Yeah. I mean, again, it's really early. Don't forget, in terms of feedback, we engaged with a lot of key opinion leaders, so we got a lot of feedback even before we launched the products in these sites. Launching nasal swab in the sites now is giving us additional feedback on the actual utility with real patients. You know, we started to launch it, as I mentioned. We've got sites already in place and, you know, we're gonna drive that up to something up to 50 clinical utility sites. I mean, that's a number we could flex either way, but right now that would be our more aggressive plan to achieve the acceleration and the patient numbers that we want to access. We've already gotten in patient samples, and so, you know, it's great to see things are happening. As a result of even those first patient samples, we've gotten some feedback on utility and ease of use and so on. Nothing new to report yet. I think it's a little early days, but as we get through the next quarter, we'll certainly have a lot more experience and possibly something more to share on the next call. Great. Thank you so much. Thank you. Thanks, Yuko. Your next question comes from the line of Matt Sykes from Goldman Sachs. Your line is open. Hi, Marc and Rebecca. Thanks for taking my questions. Appreciate it. You know, maybe just Marc first on big picture questions. Just given all the integrations that's going on and the competitive nature of the diagnostics field, I'm just wondering if you can update on the commercial field force you have now and any issues or any positives from the integration. I'm sure some of those have come with their own commercial forces, but just wondering how you feel in terms of your right size for the commercial capabilities that you have currently. Yeah, that's a great question. Thanks for asking that. We have a really strong sales team, and we've been bolstering that team in, you know, many areas. If I take each one in turn, I mean, Decipher is adding sales reps at a nice steady clip. You know, again, we've kind of, you know, Tina can talk about this if you like, but we've you know, you can't go too fast because you disrupt. It takes a while to get the sales reps trained and ready to go. You know, there's a certain optimal level, and we think we've hit that optimal level. In fact, if anything, we've accelerated that. I don't know, Tina, if you wanna comment on the sales reps for Decipher in particular. No, I think we're very picky about who we hire. We really have a very extensive interview process, and so we really are looking for the best. Also, you know, that's exactly what Marc said. You know, you don't wanna bring too many on too quickly because you've gotta keep the balance of the lab and billing and customer service all in check with your reps. I feel like we have accelerated over what we had originally planned by about three reps. Great. Thanks, Tina. Afirma is a very experienced sales team that's been with us for a while, and again, we've continued to build that sales force. You know, part of our next strategy for 2022 is figuring out how many more sales reps we need to add in that business to go after what is still a significant remaining white space. There are not enough people who are getting the Afirma test today. More patients need access, which means potentially more sales reps for us and more territories. Pulmonology, you know, because we have a broad portfolio of products and the one that is the most significant volume is gonna be the nasal swab. We have built a meaningful sales team there and continue to focus on the commercial launch of that product over the next couple of years. You know, our strategy is a little further outlooking for ensuring that that sales team continues to grow ready for the launch and the volumes that we're likely to get. We'll make sure we have enough salespeople ready to meet the demands for that product, which could grow significantly. In our other businesses, Prosigna you know is growing nicely in Europe, and we have a really good sales team over there. In the key countries, we have country managers that are leading the charge as well, and we've got some strong reimbursement capabilities, market access teams over there. Through the Halio acquisition, you know, we acquired some really good capabilities in IVD services, Biopharma and Immunoscore. Each of those businesses comes with sales and business development capabilities that we're now leveraging across, in some cases, other parts of Veracyte as well. Great. Thanks. That's really helpful color. Appreciate it, Marc. Rebecca, just one quick one for you on the gross margin side. I know when you exclude the HalioDx, it was an increase year-over-year. Just would love to kind of hear your puts and takes and what's going into that and any kind of views you have into the end of the year on the gross margin side, whether it's on the ASP or the COGS part of it. Thanks. Yeah. Happy to do so. In the quarter, as you mentioned, Matt, we were impacted by a purchase price accounting adjustment to the HalioDx business, which brought down that gross margin relatively significantly. We would expect on a go-forward basis that to normalize, and gross margins on a go-forward basis to be in the, call it, mid-ish 60% range, including the impact of Halio, which ex Halio would lend the core business, if you will, to be more in the high 60s. On a go-forward basis, you know, I think ASP is relatively stable. We've seen plus or minus a little bit towards $2,700 now for a couple of quarters. From a COGS perspective, you know, it's highly tied to volume. Assuming volume is coming through, the business, we would expect that not to be, you know, necessarily a point of conversation. Those I would say were the primary puts and takes. Our cost of materials isn't necessarily worth even mentioning, in terms of volatility at this point in time. Obviously, inflation is something we're all keeping our eye on, but currently not impactful. Great. Matt, I apologize. Thanks very much for the questions. You asked as part of your second part of your question about integration and integration effects, which I think was just more broadly than commercial. Just to make sure I address that. The integration, you know, of Halio, which was our focus for this quarter because Decipher had gone extremely well previously, couldn't have gone better in my opinion. I've been through many of these, and this is one of the smoothest I've ever seen. We had a really robust approach driven by, you know, collaborative work streams that were worked together from both Veracyte and Halio. Bonnie led the charge and is still leading the charge on that and the program office. Many things got done, whether it be in the branding and communications, HR, finance. You know, obviously, we had to close the books under a public company structure, not a private company structure. Manufacturing transition, CLIA lab, IT, which you can imagine always has a lot of integration activity to get on. Every one of those work streams did an outstanding job, and folks worked really hard. I'm very pleased with the outcome. In terms of effects and impacts, very, very few, in really, I mean, a few things along the way that we were able to tackle very quickly, but you know, outstanding result. Great. Great to hear. Thanks for taking my questions. Thanks. Your next question comes from the line of Mike Matson from Needham & Company. Your line is open. Yeah, thanks for taking my questions. With the HalioDx Immunoscore test, is there any plans or ability to leverage that into additional GI tests or other types of cancers? I mean, the great thing about Immunogram as a platform from which Immunoscore is derived as one product is it is a platform, and it does have applicability to multiple cancer types. You know, anywhere. There are a number where, you know, and in fact, there's a good Nature paper that covers this, where it is most applicable and somewhere it's less so. You know, anywhere that it could be applicable in looking at the tumor microenvironment in particular and seeing how the individual patient is responding is a potential application for the product. Yeah, there's potential. In terms of how we roll that out and what the strategic plan is for that's something that we're still working on. Vincent Fert, who is leading that, you know, across all of Veracyte now for Immunogram. Okay, thanks. It looks like your OpEx was kind of in the low forties if I strip out the one-timers, the acquisition-related stuff. Is that right? Is that kind of the run rate we should expect, you know, in the nearer term? Yeah. Thanks for the question. It was in the low thirties if you strip out stock comp, intangibles, and acquisition costs. So, I think the stock comp probably is the difference between your number and my number. But- Yeah. Just that clarification. Yes, I think, you know, as we go forward, I think that's a fair rough estimate. Obviously, ahead of 2022 planning, specifically more for the fourth quarter. Yeah. Okay. Got it. Thank you. Anytime. Your next question comes from the line of Brian Weinstein from William Blair. Your line is open. Hey, good afternoon. This is Griffin on for Brian. Thanks for the questions. Just a question on the lung cancer space. I saw Guardant announce plans for that lung cancer screening assay for smokers pre-CT. Just wanted to get an update on your NOBLE trial and your own pre-CT program there. I guess a specific one, do you have any idea what% of nodules are discovered incidentally versus as part of a screening program? Yeah. I mean, on that second part of your question first, you know, there are 15 million people who are high risk and eligible for screening under current USPSTF task force guidance. Of those 15 million, roughly one million are actually undergoing screening on an annual basis, and 1.6 million are found incidentally. Okay. So not as part of a screening regimen. In all cases, those are kind of confirmed by low-dose CT, which is very sensitive. But you know, there's kind of a very high false positive rate or number of nodules that are benign. You know, you need a test like the nasal swab to be able to help confirm whether those nodules are benign or not. That's you know, how we think about it. The NOBLE study is going well. I mean, you know, not much more to add in terms of beyond what we've said publicly about that trial. You know, enrollment's continuing and we're getting samples in and, you know, we're gonna be learning a lot from that study. That's a really important trial for us and will certainly help to open up the markets earlier on in the care continuum. Okay. Thank you. No, no. Actually, Giulia, I'm sorry, maybe I could just open up. Giulia, do you have anything to add with respect to NOBLE in particular? No, your comments were spot on. It's going very well. We're accruing, and we hope to gather 9,000 patients ultimately and follow their course over the next number of years. It's gonna be a very rich repository for us moving forward. It's going well. Excellent. Thanks, Giulia. Okay. Thank you. Just one on Decipher. Could you just talk a bit more broadly about the drivers there? You know, sales force adds, product line extensions, and then the coverage wins. Any idea on the rough magnitude of each of those? Really trying to just understand how impactful Bladder could be in 2022. Thank you. Yeah. I'll turn over to Tina. As you know, we just started with bladder, and we're very excited to have that out on the market. It's one of the first molecular tests to even be offered in bladder. Where it's really going to be used the most is in muscle invasive bladder cancer, where a lot of times now they treat with chemotherapy prior to removal of the bladder, that is the cystectomy. What they have found is that a lot of patients do not benefit from the chemotherapy treatment. It doesn't actually reduce the size of the tumor and does not help when they go to do the surgery, and as a matter of fact, can be more detrimental to the health of the patient before surgery. It's a very complex surgery. It takes a lot of time. It can be anywhere from 6-8 hours to actually do the cystectomy. Therefore, you want to have the patient in the best health possible. Most of the patients, the average age is 73. A lot of them are long-term smokers, and so their health is not good to begin with. By running our test and being able to really say which patients should and should not receive chemotherapy prior to surgery, there's a great advantage to that. It's the first of its kind. There's about 150 surgeons who really focus on doing these surgeries because, as I said, they're very complex. The good news is they're located in the same offices as our urologists who are treating prostate cancer, so therefore we're at the same place at the same time, working with the same docs, and we're using the same sales force. We don't have to have a different sales force because it just fits right in. We do have coverage from Medicare. On that, it's a little over $3,400 for Medicare, and we're actually seeing more Medicare patients coming out of bladder than we will of prostate because of the 10-year age difference between the two. We have data that was just released in The Journal of Urology, which really substantiates this study that I just told you about, of being able to Decipher which patients should get the test and should not prior to cystectomy. Prostate as well. On the prostate side, we've continued to add new sales reps every quarter. We're still seeing a lot of growth. It's amazing as I've mentioned in prior discussions that I've given, prostate is still an area that's behind as far as molecular testing, so we still have a lot of white space and there's still a lot of docs that we can go to and continue to sell them the test. At the ASTRO meeting just a couple weeks ago, it was Decipher, Decipher. There was a lot of presentations given on our test by doctors who participated in clinical trials that we ran, and that was very exciting for us to be showcased so strongly at that meeting. Obviously we keep adding to our GRID database. We're up over 100,000 patients now of data in that database, and we use that to offer additional molecular information to our physician customers as needed. I still see a lot of market runway with both of those products for 2022, certainly, and beyond. Thanks, Tina. Great detail. Thanks, guys. Cheers, Brian. Your next question comes from the line of Thomas Flaten from Lake Street Capital Markets. Your line is open. Hi, guys. This is Travis filling in for Thomas. One question I had is in regards to the HalioDx. I know you guys said that you wanna do IVD testing, development, and manufacturing operations. Could you just tell us how that process is going and just provide a little bit more color on that? I mean, HalioDx has over 15 years of experience in IVD development and manufacturing. You know, first and foremost, the manufacturing capability is gonna be used to manufacture our own kits for the platform nCounter outside the U.S. That process will take 24 months to be completed, is our current estimation. That work has already started in terms of planning for that. Now, the IVD development, which I think is a real gem here in terms of the acquisition, it's a great business that the team in Marseille has built. We can leverage that really well to actually port the test, the CLIA test that we've developed here in the U.S. over to the nCounter platform. Our own internal team has experience of doing this for customers, and we'll be able to do this for Veracyte internally. That's really exciting, and that's what I was referring to is the collaboration between our R&D teams across three sites has gone really well, and the planning has progressed nicely. Not yet ready to say which products in which order and by which date, but certainly we've got a draft roadmap for each of the products. As I mentioned in the prepared remarks, we will be porting over our Envisia test, our prostate, bladder... I'm sorry, Decipher Prostate, and as well as our nasal swab. And then other tests like bladder potentially could be candidates sometime in the future and beyond. More to come on that. Got it. Well, thank you very much for my question, and, congrats on a great quarter. Thank you. Thank you. Thanks, Travis. The next question we have is from Andrew Cooper from Raymond James. Your line is open. Hey, thanks for the questions. Maybe just first to get a little bit of clarity just to make sure I'm understanding correctly, you know, you mentioned kind of the 24-month timeframe for really porting that manufacturing over, but if we go back historically, you had talked, you know, about things specifically Envisia being a little bit faster for getting onto the nCounter platform. Is the 20-month, 24 months sort of to get something prepared for nCounter or really just to be manufacturing it yourself as opposed to relying on NanoString? And how should we be thinking about maybe the cadence there, even if you don't give exact dates for exact products, just a little more flavor would be great. Yeah. Yeah. Thanks, Andrew, for asking that because it really does, you know, help us clarify the two parallel paths. The 24 months is the manufacturing transition, so it's the latter of what you said. It is, you know, getting ourselves ready to be able to manufacture the kits out of Marseille. That is distinct and separate, but obviously interconnected with the development product projects, which is a separate parallel path, which is three individual IVD development projects to port the tests over to the nCounter platform. As you know from our previous commentary, work on that, on Envisia, had already started. We've been able to validate that the concordance between the nCounter and our existing assay was really, really high. So that is ahead of the curve in terms of progress. Of course, we have to go through that same process for prostate and for nasal swab. In addition, we've got to go through the validation and verification of the tests. We've got to go through the manufacturing connection to the manufacturing process. Of course, we've also got to be very cognizant of IVDR in Europe as well. All that has to be part of the project planning for those development projects as well. Those two things are going on in parallel. The timing of the manufacturing transition is, as I said, 24 months current plan. For the development projects, it's over the next few, three, maybe slightly more years. We're continuing to refine that plan. Okay. Helpful. Maybe just one more from me. When we think about Percepta Nasal Swab and the path there, you know, obviously soft launch right now really to build up the data like you've talked about. When you have that in hand, how do we think about sort of the stage gating for kind of full bore launch? What do you expect in terms of, you know, is it a bit by bit, or do we wanna hit the ground running as fast as we can with that product? And just how do we think about the investments ahead of sort of completion of that clinical utility data? Yeah, that's a great question. I mean, obviously the clinical utility part of this phase, as I mentioned, is very thoughtful and planned and deliberate and, you know, we need to move at a pace that is appropriate. Once we get reimbursement in that timeframe, we need to be ready for a kind of full-scale clinical launch, for a test that potentially has very significant volumes. You know, during the same time period, we will be putting in place the plans or refining the plans because much of it, you know, many of them are already in place, to build the necessary commercial capabilities and infrastructure to launch that product at scale. You know, you can kind of rest assured, I don't think the situation that we will find ourselves in is one where we're not ready for the volume. We need to make sure that, you know, we've got a good sense of what that volume is gonna be and that we're ready to absorb it. Our CLIA lab needs to be ready to process the samples, our sales team needs to be scaled up and so on. That's what the work we'll be doing over the next, you know, call it 6-12 months. Great. I'll stop there. Thanks. Thanks. There are no further questions at this time. I would like to turn the call back to Mr. Marc Stapley. Please go ahead, sir. Thank you. Thanks. I appreciate all the great questions. I'd like to take this opportunity to thank the entire global Veracyte team for their tremendous efforts and dedication as we continue to advance our business on multiple fronts. We've got now over 700 dedicated employees, and it's been really gratifying actually to see the collaboration across teams, offices and continents as we've worked together, and we'll continue to work together to build Veracyte into a global diagnostics leader that improves outcomes for patients all over the world at every step of their journey. I look forward to updating you on our progress at our next quarterly call. Thank you everyone. Ladies and gentlemen, this concludes our call today. Thank you for joining us. You may now disconnect.