Good day and thank you for standing by. Welcome to Veracyte Fourth Quarter and Full Year 2023 Financial Results webcast. At this time, all participants are in a listen-only mode. After the speaker's presentation, there will be a question-and-answer session. To ask a question during the session, you will need to press Star 11 on your telephone. You will then hear a message advising your hand is raised. To withdraw your question, please press Star 11 again. Please be advised that today's conference is being recorded. I would now like to pass the call over to the Senior Director of Investor Relations, Shayla Gorman. Good afternoon, everyone, and thanks for joining us today for a discussion of our Fourth Quarter and Full Year 2023 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 Fourth Quarter and Full Year 2023 Financial Results. This release, along with a 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 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 files with the Securities and Exchange Commission, including Veracyte's most recent Forms 10-Q and 10-K. In addition, this call will include certain non-GAAP financial measures. Reconciliation of these measures to the most directly comparable GAAP financial measures are included in today's earnings release, accessible from the IR section of Veracyte's website. I will now turn the call over to Marc Stapley, Veracyte's CEO. Thanks, Shayla, and thanks everyone for joining us today. I am pleased to share that 2023 was a record year for Veracyte. Our high-value tests improved care for more than 125,000 patients and their physicians, enabling better diagnosis, prognosis, and treatment decisions. I'd like to thank the entire Veracyte team for their hard work and dedication to our mission of transforming cancer care. Over the course of 2023, we grew revenue 22% and generated $44 million in cash from operations to deliver our second consecutive year of positive cash flow. This is a significant proof point that our philosophy to drive cash generation while investing in our strategic growth drivers is paying off, and we expect to achieve positive cash flow going forward. I am extremely proud of our strong financial profile, allowing us to further expand the impact we are having on patients' lives. Our success is attributable not only to the dedication of our employees to our mission but also to the Veracyte diagnostics platform, which refers to our unique approach to launching and driving adoption for our diagnostic tests. This is driven by broad sets of genomic and clinical data, deep bioinformatic and AI capabilities, a powerful evidence generation engine which ultimately drives guideline inclusion and durable reimbursement for our tests, as well as proven commercial excellence. The platform creates a flywheel for the generation of novel insights that in turn drive innovation and pipeline development toward future test expansion in a way that is extensible and repeatable across multiple indications. Decipher Prostate continues to be a clear example of this platform in action. Over the course of 2023, we added 8 publications and 16 abstracts to the Clinical Evidence Library for Decipher Prostate and an additional 12 abstracts and 7 publications from our research-use-only, or RUO, Decipher GRID offering. During Q4, data from multiple studies were presented at the annual meeting of the Society of Urologic Oncology, or SUO, highlighting the ability of Decipher Prostate to identify patients whose prostate cancer is likely to progress. This focus on evidence generation reinforces the test status as the only molecular test to receive Level 1 evidence designation in the National Comprehensive Cancer Networks, or NCCN's, prostate cancer guidelines. The backbone of clinical evidence supporting Decipher Prostate is clearly resonating with physicians as we delivered approximately 15,500 Decipher test results in the quarter. We now estimate that the market for molecular tests in prostate cancer is approximately 35% penetrated, with plenty of headroom remaining for growth as we believe penetration could get to 80% over time. Looking to 2024, we are focused on bringing Decipher Prostate to even more patients. We believe this will occur through indication expansion, additional payer coverage, and even more clinical studies, some of which will utilize Decipher GRID to further accelerate the flywheel of data generation and claims expansion. One example of this: we anticipate the current draft of Medicare's Local Coverage Decision policy for patients with metastatic prostate cancer to become final later this year or early next year. As a reminder, we estimate there are an additional 30,000 patients annually who could benefit from the prognostic and predictive information Decipher delivers to clinicians at pivotal moments in their journey to treat cancer. Moving to Afirma, this was another record quarter for tests delivered. We reported approximately 15,200 Afirma results, with growth driven by new and existing accounts, including competitive wins. Over the course of the last two years, we have continued to enhance the Afirma offering, adding TERT promoter mutation testing, enhancing the online physician ordering portal, and introducing the Afirma GRID RUO tool. While GRID for Afirma has only been available for a short period of time, the promise of advancing science in developing prognostic signatures has been well received by customers focused on research. Many have proactively reached out and are interested in collaborating to publish and fully validate new signatures. These launches and enhancements led to increased popularity and adoption of Afirma over the course of 2023, which represented a record growth year for a product which launched more than a dozen years ago. Looking to 2024, we expect Afirma to deliver solid growth through three key mechanisms. First, continued execution to further drive penetration into both existing and new physician accounts. Second, engaging with MolDX on their draft LCD to cover Bethesda V patients who could also benefit from insights provided by Afirma. And lastly, scientific engagement empowered by GRID and an enhanced customer experience to ensure that we maintain and grow our community of dedicated physicians. Decipher and Afirma are great illustrations of the Veracyte diagnostics platform in action. This proven approach will enable our long-term growth across three vectors: global expansion, solving new cancer challenges, and, with the acquisition of C2i Genomics earlier this month, serving more of the patient care journey. With our Percepta Nasal Swab test, we are focused on tackling new cancer challenges. We believe the test will benefit patients and physicians as a non-invasive option to help guide clinicians' next steps for patients with potentially cancerous lung nodules. During the quarter, we made significant progress publishing the clinical validation data for the test in the journal CHEST and bringing the number of sites enrolling for the NIGHTINGALE clinical study close to 100. NIGHTINGALE is designed to demonstrate clinical utility and support reimbursement for the test and remains a key focus in 2024 as we expect to complete patient enrollment in the summer. The level of interest demonstrated by the large number of sites that have engaged in NIGHTINGALE gives us optimism in the value the Percepta Nasal Swab test could bring to physicians and their patients. Shifting to our focus on global expansion, our strategy to deliver IVD versions of our test to physicians and their patients outside of the United States is another key long-term growth driver. Over the last quarter, we have largely completed the transfer of kit manufacturing for our ProSigna breast assay from NanoString to our Marseille, France, location. With this transition, while we maintain some near-term dependency on NanoString for component supply and instrument service, we have worked through mitigating most of the supplier issues we began experiencing in the second half of last year. As a result, Q4 ProSigna volumes were ahead of our prior expectations. Looking forward, we're monitoring the situation and doing our best to ensure continuity wherever we remain dependent on single-source suppliers. As we shared previously, we are now executing on a multi-platform IVD approach where we leverage the quality of our diagnostics and the level of evidence supporting them to differentiate us. We are focused on key product and market development activities that will help drive a steady cadence of IVD test kit launches over the coming years. We will soon submit our existing ProSigna test for approval under the IVDR framework, which is a key step to catalysing launches across our oncology IVD portfolio. From there, we expect Decipher Prostate to launch in mid to late 2025 on PCR, and an updated NGS-based ProSigna test around the same time to be launched on NextSeq 550Dx. We continue to expect Percepta Nasal Swab to be commercially available in 2026 on NGS. Turning to serving more of the patient care journey, we recently closed our acquisition of C2i Genomics, and I'm thrilled to welcome the C2i team to Veracyte. This acquisition enables us to enter the minimal residual disease, or MRD, market and expand our role across the cancer care continuum, building from our position in early diagnosis and risk assessment to treatment monitoring and disease recurrence testing. C2i's novel, whole genome sequencing approach to MRD fits well into the Veracyte diagnostics platform, making it the ideal solution for us to address this portion of the patient journey. First, the assay requires less than 4 ml of blood, much lower than many competing tests. Second, the rapid generation of patient-specific signatures available almost immediately after the whole genome assay is performed is faster than bespoke panels that take weeks to develop. Third, the approach takes the widest possible view of the tumor genetic landscape to deliver performance that we believe enables earlier detection versus imaging and other molecular tests. By identifying the effectiveness of a treatment almost real-time, the physician can rapidly tailor the care plan for a patient, which we believe will lead to better outcomes. And because C2i's technology uses whole genome sequencing, we get more data for evidence development, giving us a rich view of tumor biology that allows for more collaborations and will catalyze further discoveries. As we mentioned when we announced the acquisition, we will commercialize MRD first in muscle-invasive bladder cancer, where we expect to launch a test in the first half of 2026, leveraging the same strong urology channel that has delivered continued growth in Decipher. I am excited about our trajectory, and even more by the impact we are having on physicians and their patients. With that, I will now turn to Rebecca to review our financial results for the quarter and expectations for 2024. Thanks, Marc. Q4 was another record quarter with $98.2 million in revenue, an increase of 22% over the prior year, higher than our pre-announcement due to the finalization of cash collections, which benefited ASP. We grew total volume to approximately 34,000 tests, a 21% increase over the same period in 2022. Testing revenue during the quarter was $90.4 million, an increase of 29% year-over-year, driven by higher-than-expected Afirma volume, Decipher growth, and strong prior period cash collections. Total testing volume was approximately 31,000 tests. Testing ASP was approximately $2,900 as we resolved and collected over $4 million of out-of-period payments. Adjusting for this impact, testing ASP would have been approximately $2,750. Fourth quarter product volume was approximately 2,600 tests, and product revenue was $3.7 million, up 13% year-over-year as the team did a tremendous job limiting the patient impact of the supplier issues Marc mentioned. Biopharmaceutical and other revenue was $4.1 million, in line with our expectations and down 39% year-over-year given overall spending constraints across the industry. Moving to gross margin and operating expenses, I will highlight non-GAAP results, which exclude the amortization of acquired intangible assets, other acquisition-related expenses, and restructuring costs, but does include routine stock-based compensation. Non-GAAP gross margin was 70%, up approximately 340 basis points compared to the prior year. Testing gross margin was 73%, up 90 basis points compared to the prior year, benefiting from higher lab volume and over $4 million of out-of-period collections. Product gross margin was 52%. Biopharmaceutical and other gross margin was 15%, down year-over-year due to lower fixed cost absorption. Non-GAAP operating expenses, excluding cost of revenue, were up 28% year-over-year at $65.6 million, including a $3.5 million technology access fee to develop our IVD-kitted test on the NextSeq 550Dx NGS platform. Research and development expenses increased by $7.6 million to $18.7 million due primarily to the tech access fee and increased costs related to our NIGHTINGALE and Decipher clinical studies. Sales and marketing expenses increased by $1.8 million to $25 million. G&A expenses were up $5.1 million to $21.9 million, driven by higher personnel costs and infrastructure-related investments. We recorded a GAAP net loss of $28.3 million, which included $32 million associated with the impairment of HalioDx biopharmaceutical intangible assets, $7.6 million of stock-based compensation, and $6.3 million of depreciation and amortization. We increased our cash position by $14 million from the prior quarter and ended 2023 with $216.5 million of cash and cash equivalents, 21% higher than the balance of $178.9 million at the end of 2022. Turning now to our 2024 outlook, we are maintaining our total revenue guidance of $394 million-$402 million. This reflects year-over-year testing and product revenue growth of 13%-15% and a decline of approximately 50% in biopharma and other revenue, as we have not seen evidence yet of an improvement in the market. We expect the non-GAAP gross margin to be in line with 2023 as tailwinds from operational testing efficiency efforts and fixed cost leverage roughly offset the annual supplier list price increases, merit, and the benefit of more than $10 million of out-of-period collections in 2023. We are also maintaining cash guidance and expect to end 2024 with between $230 million-$234 million in cash, cash equivalents, and short-term investments, including $8 million of one-time acquisition-related items. As always, our cash commentary is barring potential M&A. Moving to the first quarter, we are forecasting a sequential decline in total revenue given the impact of cash collections in the fourth quarter and typical seasonality. Additionally, we expect non-GAAP operating expenses to be higher sequentially given the impact of the C2i acquisition and the annual reset of taxes and merit. For the quarter, excluding the benefit of acquired cash and customary closing considerations from the C2i acquisition, we are forecasting a slight usage of cash due to the usual timing of compensation payments. I am excited about the momentum we have heading into 2024 and our commitment to executing on our strategic priorities over the course of the year. We'll now go into the Q&A portion of the call. Operator, please open the line. Thank you. As a reminder, to get in the queue, press *11. Wait for your name to be announced. To remove yourself from the queue, press *11 again. One moment for our first question, please. It comes from the line of Sung Ji Nam with Scotiabank. Please proceed. Hi. Thanks for taking the questions, and congratulations on the quarter and a great year. Maybe just kind of kick off with the TERT promoter mutation capability that's part of Afirma. Could you give us a sense of kind of what percentage of the volume that would actually be useful for that particular testing of the Afirma volume? Yeah, Sung. Thanks very much for your kind comments. It was certainly a great year. On TERT itself, it's a relatively rare condition, and so the percentage of patients that actually show up with that mutation is quite small. Having said that, it's proving to be extremely useful to order that test, certainly in a larger number of the cases. I don't actually know if we've got the percentage that we're currently seeing. I don't know if you have that. Yeah. I believe it's ordered approximately 20% of the time where we have a positive result with Afirma. But the actual percentage that has the mutation, in my recollection, is more in the single-digit type range. So that just gives you a sense of how frequently it is being ordered and how frequently it is being seen. I think, importantly also, TERT is a competitive differentiator for us with regard, and we aren't necessarily seeing an ASP uplift from TERT because it is not something we necessarily have coverage for. But to Marc's point, it's more about the overall clinical contribution of having the assay than it is about a financial contribution to the company. It's more about the patient benefit. Yeah. And one of the ways I really think about how having that capability has helped our Afirma team and our Afirma business in particular is it's really given our sales team yet another reason to go and engage with their customers. It's enhanced our test relative to both the competitive landscape and also where we think, ultimately, guidelines can go. And so we always thought it was important to include that as part of the Afirma. And Sung Ji, I apologize. I said 20%. It's actually more like a third. Oh, okay. Wow. Okay. Fantastic. Super helpful. And then my follow-up is just on you mentioned the C2i. The first indication is going to be in the muscle-invasive bladder cancer. Could you guys remind us about Decipher Bladder, the genomic classifier, and kind of how does that kind of go hand in hand with your MRD offering or the plans for the MRD offering? Do you think there could be synergies there? Just kind of how should we think about the Decipher Bladder platform? Yeah. I mean, there are always going to be synergies whenever we can continue to increase the menu of offerings and tests that we have in the urology space. As you know, a few years ago, we launched the bladder test. It's more of a subtyping test to help potentially determine course of treatment. But what we're and it's had relatively low penetration, and we didn't particularly drive that commercially, one of the reasons being it is while it's the same call point, it is a completely new product if you think about it like that. And so we do not want to distract and never wanted to distract from the benefit that we're seeing in Decipher Prostate. But the clinical utility is ultimately what matters, and we're continuing to develop that test further and think of ways of enhancing that utility. But we've really refocused our energy now in bladder on the MRD test at this point. We think that the market opportunity for a muscle-invasive bladder cancer test in MRD, which has a clear path to reimbursement, is greater. And we're going to launch a test in the first half of 2026. And so that's where you're going to see our investments in both our R&D and development activities and then ultimately in our commercial activities as we put that test in the hands of the existing urology salesforce. But beyond that, one thing you'll continue to see us do is and we've talked about this quite a bit before is work across the patient's care continuum. And so as we can come up with other helpful diagnostic tests that have utility in either reducing unnecessary procedures or accelerating treatment or predicting the performance of surgery or therapeutic actions, we'll continue to do that. So continue to consider that an important part of the urology roadmap. Got it. Great. Thank you so much. I'll get back in the queue. Thanks, Sung Ji. Thank you. One moment for our next question, please. It comes from the line of Tejas Savant with Morgan Stanley. Please proceed. Hello. This is Yuko on the call for Tejas. Thank you for taking our questions. I wanted to ask a couple of questions on the C2i MRD assay. What remains to be done prior to launch in first half 2026, and what are the gating factors there? And is there any levers you could pull to pull forward the launch timelines? Sure. And thanks for that question. Yeah. There's quite a few steps that we need to go through here. One, of course, is the integration of C2i, which is very much in progress at this point. That team is now part of the Veracyte team. And then the systems and other integration activities will continue through the early part of this year. Then there's the launch of the product program itself, the muscle-invasive bladder test, which is entering into our normal product development process. That's kicking off now that the team is part of Veracyte. Then we're going to have to continue to run samples on that test to further validate the test and then do the tech assessment that we need to go through in order to get reimbursement. Then there's that period of waiting for a response on that as well. Quite a few different steps, steps that we have quite a lot of experience in following and have been through a number of times before. To your question on is there a way to pull it forward, if there was, we will. If there is, we will. We've provided a timeline that we feel comfortable with given all those steps. Along the way, if there's any opportunity to go faster, I think you can rest assured that the team is looking for it. And of course, that's a conversation we talk about a lot. So yeah, that's where we are right now. But no change in the plan of record first half of 2026. Thank you for that. And then I wanted to also ask about how many genomes have a C2i sequence to date. And as you think about volumes ramping, you'll be generating significant amounts of data. How are you thinking about monetizing that dataset over time? Yeah. So good question. I don't actually have the number in front of me, but it's significant. C2i have been doing this for a number of years, 5 years or so. And as you've seen from a lot of their publications, they've looked at a number of different indications, bladder being one of them. And in each of those indications, they've got a significant amount of whole genome data. In terms of monetizing that data, I think of it very much in the same way as I think about the overall Veracyte diagnostics platform. We've been generating whole transcriptomes in endocrinology, in pulmonology, and in urology for a while. C2i has been generating whole genomes. So we now have an incredibly rich dataset available to us. We, of course, get interest from biopharma and expect to continue in the future. I think particularly with MRD as an asset that continues to grow, that's not our primary focus. Our primary focus is very much on our diagnostics pathway. Opportunistically, as we have contact with biopharma who are interested in any of that dataset I've described, we'll follow up on those opportunities. We clearly have some in the pipeline right now. We've had some in the past, and we'll continue to explore that. You can imagine a scenario where in the future, the C2i MRD assay acts very similarly to Decipher GRID and Afirma GRID where we are continuously generating clinical utility and other studies, which broaden our potential indication expansion and therefore also subsequently help our commercialization efforts and managed care efforts. And so I absolutely agree with Marc. But effectively, when it comes down to the diagnostic platform we have described, this kind of whole X approach, whether it's whole transcriptome or whole genome, really does allow us to monetize these markets more quickly and get a stickier response given the differentiated approach we've taken here. So just add that to Marc's commentary. I think there's a couple of different ways we could see this play out, both of which are obviously quite positive. Thank you very much. Thank you. One moment for our next question, please. It's come from Mason Carrico with Stephens. Please proceed. Hi. Yeah. Thanks for taking our questions. This is Jacob on for Mason. Maybe just starting with your guide, could you just help us think through what's embedded in your guidance for 2024? And maybe more specifically, what are the puts and takes that could play out in 2024 that gets you to the high end versus low end of your guide with respect to Afirma and Decipher growth? I know you said you're expecting testing and product revenue to grow 13%-15%, but maybe just breaking that out a little bit more and giving us more color would be helpful. Yeah. Happy to. You're absolutely correct. We're expecting testing and product revenue growth to be 13%-15%, thereby absorbing a good portion of the biopharma decline of approximately 50%. When you break down Afirma and Decipher, I think the easiest way to think about it is they're at very different stages of their life cycle. And as a result, as well as the comp on the Afirma side, obviously, when it comes down to it, the Decipher growth will be higher than the average of the two, and Afirma will be below the average of the two. We're not going to get into the expectation to a point range at this point in time, but I think the most important thing to know is we are very confident in our ability to penetrate both of these markets up to the 80% level. And while we have significant out-of-period headwind from prior period significant. We have significant prior period collections as a headwind, third time's a charm. We are still very confident in the growth and overall trends of both of these products. I think importantly - and I mentioned this in the prepared remarks - for the first quarter, we do expect a slight difference between the two in seasonality, and that is worth noting. On the Afirma side, we saw, obviously, quite a strong fourth quarter. And so we are expecting a sequentially down quarter for Afirma, maybe even a little more than we had seen in prior years given some of the weather impacts so far year to date. And Decipher, we are expecting to grow. And so just a little bit more guide, more color into the Q1 guide, I think perhaps that could also be helpful. Got it. Thank you. Yeah. That's helpful. Then I guess just on Decipher Prostate more specifically, what are you seeing in terms of competition in the prostate market? Have you started to see any shift in competitive dynamics? Do you still feel like you're taking share? And I guess you guys noted that it's 35% penetrated in the market right now with potential to reach up to 80%. How much of that is kind of dependent on this MolDX LCD coming through at the end of this year and into next year? Yeah. I mean, to cover that second part first, obviously, not a great deal. That is, as I mentioned, it's about 30,000 patients a year. So certainly very important. It'd be great to get that LCD. It'd be more great from the patient outcomes perspective to be able to benefit from the Decipher test in that way. But really, if I think about it, the most important thing we're focused on is how we continue to drive Decipher Prostate and gain that market share. More importantly as well, also to penetrate more of the market as we do that. Because honestly, at this point, with so many patients who have prostate cancer still not getting our test or any other test, I think that's definitely a concern from the patient's perspective. With the level of publications that we've seen for Decipher and that we've generated, not to mention all of the clinical and research publications that I referenced today in the prepared remarks, plus the NCCN Level 1 guidelines, the vast array of experience that people have not just in the U.S. but globally with Decipher, we're doing everything that we can in order to drive further penetration and continue to be the market leader. So, I haven't seen, yeah. I I wouldn't say there's any change in competitive dynamics one way or the other. We're very focused on what we can do to have the most effective test. And then beyond the U.S., I mean, those are all U.S.-related comments and U.S. market shares. But beyond the U.S., there's so much KOL experience outside of the U.S. in terms of experience with studies involving Decipher. We feel there's a pent-up demand for that. So as soon as we can get our Decipher product launched on PCR, which we're planning to do in end of 2025, I think our expectations for the adoption there are a little bit more optimistic than they otherwise would be had we had to go and create a market or a level of interest from scratch. So lots of excitement on our side for Decipher going forward. All right. One moment for our next question, please. It comes from the line of Dustin Scaringe with William Blair. Please proceed. Hi everyone. Good afternoon, and thanks for taking our questions. First here nasal swab, you guys published validation data in December. Just wondering if you can talk about the feedback you've received on that since publication. And then as a follow-up to that, how are you thinking about the TAM here given this was validated on individuals that had some sort of smoking history? Thank you. Yeah. Great questions. So the data that we ended up publishing or getting published in CHEST in December is data that we'd shared previously, actually, a couple of years ago. So getting it into a final publication, I think, is an outstanding outcome. And I congratulate our entire team and others that we worked with on that publication. It's great to finally see it out there. In terms of level of interest, I think the publication really does a couple of things for us. One is it helps us to really commence those reimbursement conversations and start to get ahead of that. We now have a peer-reviewed publication in hand to do that. It also helps us have conversations with potential partners and others who might want to do some work with nasal swab in the future. So very excited about that. But really, where I kind of hang my greatest sense of the level of interest in nasal swab so far is in NIGHTINGALE. Because as I mentioned on the call, with close to 100 sites enrolling, the level of interest in those sites if you think about what it takes from a clinical operations standpoint to identify, gain interest from, contract sign-up, initiate, and then commence enrolling at nearly 100 sites, it's significant. And it can only come from those investigators and those institutions being excited about the prospect of the test itself and being a part of that clinical utility study. So that, to me, I think is so far one of our greatest indicators of interest nasal swab. and we're excited to see how that goes and certainly have a desire to see the clinical utility come out of that study. Understood. Staying on that topic for a while. Oh, yeah. Sorry. You did ask I'm sorry. You asked about the market size for TAM and smoking history. I should cover that. Yeah. Just to be really clear, I mean, nasal swab is based on smoking patients who have a smoking history. It really measures the damage to the epithelial airway. One cause of that damage is, of course, smoking. To expand the TAM beyond that would require a study that includes nonsmokers. And that is not the biggest market we're looking at. By far, the largest market is those patients who are eligible for lung cancer screening and those who have lung nodules incidentally found, which are 15 million and 1.6 million, respectively. That, by far, is the biggest market. And a significant proportion of those are current or former smokers and would fit the eligibility criteria for nasal swab. A next step in the future could very well be trying to expand that TAM by doing the necessary studies outside of nonsmoking. We just don't know whether that's until you've done the study, you don't know whether that actually produces the same results or not. But by far, we've focused the product initially on the largest proportion of the market. Understood. Thank you for that. And switching over to Afirma, just wondering if we should be thinking about any reimbursement dynamics for the test in 2024 and then any considerations longer-term about pricing for this product. Thank you. Yeah. Happy to take that. So Afirma, if you rewind the clock back to 2021 with the code change, we did see the impact in 2022 of that. And then over the course of 2023, we did see, obviously, the benefit of resolution of many of those impacts of 2021 and 2022 tied to the code change. The reason why I go back throughout all of that history is the ASP for Afirma at this point in time, based on those resolutions, is quite elevated. I think when it comes down to it today, we're in a great position. Our goal is to maintain that position. We see no reason why we can't continue to do so. We had some smaller managed care wins over the course of the back half of last year that really help us be confident that we'll be able to maintain ASP plus or minus a bit as we see any given quarter. I think on the Afirma side, not any big dynamics to think through. From a PAMA reset perspective, that doesn't come to bear until 2028 as well. So we feel great about the work the team has done, both on the managed care and the billing side and collection side. And I think we're going to be, obviously, quite focused about that going forward. Over the course of I think also, it's worth highlighting on the Decipher side, obviously, less of a dynamic with a code change like we had on Afirma, but I think a different portion of the story given it's more nascent in its coverage and contracted lives. And so we do have a very good story on the Decipher ASP. We've gotten a number of wins over the course of 2023, and we're hopeful we'll have some more over the course of 2024 and 2025. And so we're obviously hoping that we can continue to progress the coverage for Decipher given, effectively, the Level 1 status that it has and the publication and clinical support it has. Appreciate all the color there. Thank you. Thank you. One moment for our next question. It comes from the line of Matt Sykes with Goldman Sachs. Please proceed. Hey, guys. Congrats on the quarter. Thanks for taking the question. Is there any way to quantify how much benefit you see from your established commercial infrastructure with Decipher Prostate and how much of that can be applied to your bladder MRD test? Yeah. It's a great question. I mean, the leverage that we're getting out of our urology sales force in prostate alone has been very significant. And I think you see that in the numbers. We added less than a handful of net total reps in last year, and you can see the significant growth that we got out of Decipher. One of the reasons we think there's a lot of reasons why we actually think an MRD-based test in bladder is the right test for us, not to mention the cohorts that we've got, the work that's been done already. But really importantly is leveraging that urology sales force again. And it goes back to the comments we made, and I think it was in response to the first question. There is the benefit of having more and more menu available for our reps as they go out. And they've got these fantastic relationships with the urologists from large group practices all the way down to the community, being able to offer their patients who are dealing with bladder cancer, which is a terrible prognosis in many cases, and having something to offer to them to enable to determine whether or not their treatment has been or is being effective; it will be incredibly meaningful. So we do think we'll be able to leverage the existing sales force that we have and will have at that time without having to grow it substantially. While it might be within a practice, there might be a dozen urologists, and maybe one of them specializes in bladder cancer. And so you might find that it's a different sell; it's a different product sold to a specific specialty within that practice. The reality is we have incredible access to those practices in general. So we don't anticipate a great deal of extra investment required in order to sell our test in the channel. Agreed. I would just add one more thing. Obviously, the Decipher franchise extends into the revenue cycle management and client services piece and all the infrastructure to order the test, which has been, obviously, now invested in and will sustain and also benefit from office staff using historically. That should also help the commercial efforts on the MRD side, the knowledge and awareness of those types of interactions. Got it. Thanks. That's really helpful, caller. I know we touched on it earlier, but this is helpful. Then how durable do you see Afirma growth as once the thyroid cancer diagnostics TAM has reached that 80% penetration? Do you have a specific timeline to that penetration mark? We don't have a timeline. But if you think about it, Afirma's been on the market for more than a dozen years at this point, and it's taken that long to get to the penetration that we've currently got. With an 80% estimate out there, there's multiple years of growth still left in Afirma just to target the conditions that we currently cover and the indications that we currently have. And as you know, we've been investing heavily in Afirma. We invested in TERT, as we talked about during this call. We invested in the physician ordering experience and portal. We just launched the Afirma GRID. And so time after time, we're creating new opportunities to engage with physicians and convince even more of them to use Afirma more often in more cases. And so we're gaining wins in terms of both existing accounts and new accounts. And so it's hard to put a time frame on when that plateaus, as everything eventually always does. But it's clear that we've got a lot of a fairly decent amount of headroom still to go, even in endocrinology. Got it. Thank you. Thank you. One moment for our next question. It's from the line of Mike Matson with Needham. Please proceed. Hey, everyone. This is Joseph on for Mike. I guess just looking at other kit development, you obviously guys have a lot on your hands with Envisia, Decipher, and now C2i. But just maybe wanted to ask a question more broadly if there's any other disease areas you guys are focusing on for future test development or, I guess, if it's more focusing on MRD versus a diagnostic assay. Just kind of wanted to get your thoughts on that. Yeah. It's a great question. If you think about it, Veracyte really come from that single product, Afirma company, to a broad cancer diagnostic company. And now with the addition of MRD, we can go even further. If you think about the growth factors that we've talked about, I'll start with geographical. So the success that we've had in the U.S. with our launch of our IVD products outside the U.S. and our clear roadmap of what really amounts to three or four products that we're going to launch over the next few years there, you can see that we've got a real opportunity to grow outside the U.S. and really demonstrate that the model that we've adopted works and that has been so successful for us with the extensive publications behind our test can benefit us outside the U.S. as well. So that's number one. The second one is across the care continuum. I wouldn't say we're going to focus on any area in particular rather than the entire care continuum for patients who have cancer or are suspected of having cancer, all the way from nasal swab, which is focused on those patients who don't have a cancer diagnosis but have a lung nodule and therefore are at risk, and helping to classify those patients. Almost think of that as part of a high-risk screening program, all the way through diagnosis, prognosis, prediction. You're starting to see Decipher move into that prediction space in a very meaningful way as there are more and more publications that talk about the virtues and the benefits of using Decipher in that way, all the way through to treatment recurrence and monitoring. And so, as you think about it that way, we are able to cover a very broad part of the care continuum, everything but screening for healthy people if you think about it that way. And then the third dimension is the indications. And Veracyte has thyroid, prostate, breast, bladder, lung. And now with MRD, you can think about how much more extensible that could also be across other indications. So one of the great benefits of the platform that we've got, the large amounts of data that we generate, is that we can, that is, extensible across other indications as well. Of course, there are always channel considerations you have to go through there and think about as well. And we do and will. But you can certainly see there's opportunities for us to expand beyond the current indications that we have. No clarity yet on what those might be, but that's certainly something we're very focused on. Okay. Yeah. Great. Obviously, the one-stop shop goal. But maybe just one more, looking at C2i, I guess their platform is CE marked in Europe. I guess, A, wondering what's the indication or use case for that. I imagine it's mostly used in clinical trials right now. But maybe if there's any strategic partnerships that are ongoing or prospects in Europe that you guys are still pursuing after the acquisition? Well, there are some existing. And of course, there's a pipeline as well. And we're very selective about what makes sense for us to continue to pursue. And as you can imagine, that's been a very key part of the acquisition and integration conversations. Our approach with the test, especially with the bladder test, is going to be an LDT type of approach. to be determined if we kit that as an IVD in the future. That's certainly not the plan right now as far as the initial focus is to launch it as a lab-developed test in the way that we've described and leverage the platform that we've built there. So more to come. Again, that is, again, another expansion opportunity. And when I talk about geographic expansion and how MRD can play in that, there is a lot of optionality for us in terms of how we might use that in the future outside the US. Okay. Great. Thank you for taking our questions. Thank you. One moment for our last question. And it comes from the line of Puneet Souda with Leerink Partners. Please proceed. Yeah. Hi, guys. Thanks for the questions. So yeah. Hey, Marc. Just first one on, I know VCYT has been asked about, but just maybe what is the level of investment that you're expecting here this year? And And wondering if you can provide anything for next year sort of before you launch this assay. And how should we think about gross margin given that this assay, when it does start scaling up, it does require multiple whole genomes initially and then whole genome with repeat assays, if my understanding is correct? And maybe just on that point, just help us also understand how do you want investors to appreciate Veracyte's position in the MRD market? This is a fairly competitive market in its emergence, and there's a leader in the market already. So maybe just conceptualize so that we understand how Veracyte is going to be positioned here in MRD. Yeah. And Puneet, thanks for that. If you don't mind, I'll answer the third question first, then I'll answer the first question, and then I'll let Rebecca answer the second question on gross margin. But yeah. And thanks for asking this. I'm glad we had an opportunity to go through this. I talked about this a month or so ago when we announced the acquisition of C2i. What we really like about this solution, not to mention the incredible team, but they have built a product that fits so well with the Veracyte diagnostics platform that we're referring to. It is a whole genome-based approach, which means we get that rich data for every single patient. And not only is it whole genome for that landmark, but it's whole genome for every subsequent sequence that we do. And so incredibly rich data. The test performs extremely well. It requires a low input of blood, 4 ml. You don't have to create this bespoke assay as well, which speeds up time, turnaround time, time to answer. And then a great performance that results in, as we believe, better outcomes for patients. So there's so much about the C2i MRD product in particular that we like that fits into Veracyte, not to mention that it's going to play really well into the bladder market where we have a channel and a clear path to reimbursement. So that's how I see now. It is a crowded space. But again, our approach to a specific indication that we have, that channel, is really, I think, a very significant differentiator in addition to all the other things that I just mentioned. In terms of the investment, we've done I think a really important thing here is we've acquired C2i and absorbed and refocused our investments and absorbed the project to develop the MRD test for bladder into our current portfolio. And as you know, we've done a really focused approach to portfolio management over a number of years, and that's enabled us to do this. And that's why we gave the guidance that we gave when we announced the acquisition, that this does not change in one way our philosophy around profitability and cash generation in particular. And so without giving an exact figure on what we're investing because not only have we acquired an MRD asset, we've also acquired AI capabilities that we were going to invest in anyway, it's just, I think, fair to say it's absorbed in everything that we're doing. You want to talk about gross margin? Yeah. Happy to. And just one thing to add, Puneet. We have also said in the future, to answer your question for next year, in the future, we will continue to be generating positive cash flow. And so I think to any extent, we'll be absolutely continuing to follow the financial philosophy we have shared with you all time and time again in the future as we go forward with MRD and any other activities that we decide to pursue. With regard to gross margin, you're absolutely correct. It is a multiple whole genome assay over different periods of time. But we've looked at this very closely, as you would expect, ahead of the acquisition. And we believe, both between the ASP that we're expecting as well as the lab efficiencies that we think we can deliver, we're expecting to have a gross margin that's very reasonable, perhaps not all the way to our current corporate gross margin average, but very reasonable and something that we think more than is worth doing for the organization and can sustain a profitable business similar to how we have with Afirma and Decipher over time with, obviously, volume going through both the lab and the channel. So it will take a little bit of time to ramp there. But I think over time, we will get to exactly where we want to be from a gross margin perspective, and we're confident to that end. Got it. Okay. That makes sense. And then just briefly on the FDA's expectations to regulate the cancer LDTs, any latest thoughts from your end and anything changes spend-wise or OpEx-wise from your perspective if that was to be implemented? At this point, no changes. One of the things I'd say about Veracyte is we're very well prepared for that because our lab-developed testing process and our quality systems are very, very robust, well-proven. The publications behind our tests, as we've talked about at length, are very extensive. And so as I think about it, we're the kind of lab, and we have the kind of tests that I think fit well into any kind of model that they come out with. Clearly, we'll need to invest in the multi-stage process that ultimately gets launched. There would be some level of investment, but I don't think as great as many others who've got to kind of create that backdrop that we've got would have to incur. So we're quite comfortable with where we are there. We've got the optionality. We've got the experience of IVD development. So I'm not overly concerned about the pathway. We're as involved as others, as you can imagine, in trying to help comment on that, respond to that, and shape the way that that actually ultimately gets launched, so. Got it. Okay. All right. Thank you. Thank you. And as I see no further questions, I will turn it to Marc Stapley for final comments. Great. Thank you, Carmen. I appreciate it. So as you can all see, we ended a very strong year in 2023, and we've set ourselves up well for continued growth in 2024 and beyond. I believe our success will continue to hinge on three core pillars of execution: meaningfully expanding the markets we serve, utilizing our established Veracyte diagnostics platform across geographies, indications, and the care continuum, embracing the best technology, adding new capabilities such as MRD and AI to our world-class platform, and driving revenue growth with a discipline and a focus on profitability and continued positive cash generation. These tenets will allow Veracyte to continue to build a strong foundation for growth while achieving our vision of transforming cancer care for patients all over the world. I would like to thank our entire team for their commitment, hard work, and passion. It is fueling our progress and driving our results. So thank you. Ladies and gentlemen, this concludes our call today. Thank you for joining us. You may now disconnect.