Good day, ladies and gentlemen, and welcome to the fourth quarter 2023 Illumina Earnings Conference Call. At this time, all participants are in a listen-only mode. After the speaker's presentation, there will be a question-and-answer session. Please be advised that today's conference is being recorded. I would now like to hand the conference over to Salli Schwartz, Vice President of Investor Relations. Hello, everyone, and welcome to our earnings call for the fourth quarter and year-end 2023. During the call today, we will review the financial results we released after the close of market and offer commentary on our commercial and regulatory activity, after which we will host a question-and-answer session. Our earnings release can be found in the Investor Relations section of our website at illumina.com. Participating for Illumina today will be Jacob Thaysen, Chief Executive Officer, and Joydeep Goswami, Chief Financial Officer and Chief Strategy and Corporate Development Officer. Jacob will provide an update on the state of Illumina's business, and Joydeep will review our financial results, which include GRAIL. As a reminder, GRAIL must be held and operated separately and independently from Illumina, pursuant to the transitional measures ordered by the European Commission, which prohibited our acquisition of GRAIL under the EU Merger Regulation. This call is being recorded, and the audio portion will be archived in the investor section of our website. It is our intent that all forward-looking statements regarding our financial results and commercial activity made during today's call will be protected under the Private Securities Litigation Reform Act of 1995. Forward-looking statements are subject to risks and uncertainties. Actual events or results may differ materially from those projected or discussed. All forward-looking statements are based upon current available information, and Illumina assumes no obligation to update these statements. To better understand the risks and uncertainties that could cause actual results to differ, we refer you to the documents that Illumina files with the Securities and Exchange Commission, including Illumina's most recent Forms 10-Q and 10-K. With that, I'll now turn the call over to Jacob. Thank you, Salli. Good afternoon, everyone. As you know, I joined Illumina as CEO a little over four months ago. In this time, part of my focus has been on meeting with customers to understand their priorities, hear their feedback, and develop more collaborative relationships. Our customers think highly of Illumina and our solutions, and they want to work in strategic partnerships with us to move the whole NGS ecosystem forward. Now that we have announced that we will divest GRAIL, it has been easier for our customers to plan what their future looks like with Illumina. These meetings have been instructive and inspiring. During my recent trip to Europe, I was able to see firsthand how we are working with our customers, governments, and the broader genomics community to accelerate whole-genome sequencing adoption safely and more effectively, and to understand rare diseases and cancers as a part of the standard of care. I've also learned about Germany's model project that aims to fully integrate comprehensive genomic testing into the healthcare system there, beginning in Q2 this year. Within the hallways of our headquarters and in several global offices, I have also been connecting with our talented employees, who are committed to driving innovation and continuing to build out the genomics ecosystem. I've also had an opportunity to engage with many of you at recent investor conferences. These conversations are informing my leadership agenda and importantly, having reinforced my confidence in Illumina's core business. 2023 was a dynamic year for Illumina. NovaSeq X has been the most successful high-throughput product launched in our history. We ended the year with 352 NovaSeq X shipments, above the 330-340 we expected, amid a challenging macroeconomic backdrop that we saw many of our customers remaining constrained in their purchasing decisions. In the fourth quarter, we delivered higher-than-expected consolidated revenue of approximately $1.12 billion. Americas revenue, which is more than half of our business, was flat year-over-year. Europe revenue was up 17% year-over-year on a relatively easy prior year comparable. EMEA revenue declined 1%, although that included a 10 percentage point impact from sanctions in Russia. Greater China revenue was down 13% year-over-year, reflecting continued geopolitical challenges and local competition in mid-throughput. As I've noted before, China and our customers there are important to Illumina. We've already taken certain pricing and other strategic actions that are beginning to yield results. We will share more specifics on our progress there over time. Globally, we expect our customers will remain cautious, and for now, we continue to expect 2024 results to look very similar to 2023. While some macro headlines are encouraging, we haven't yet seen that translate to increased investment in our industry and therefore have not reflected it in our guidance. Joydeep will take you through more details in our guidance in a few minutes. While we cannot control the external environment, the management team and I remain committed to accelerating value creations across the enterprise. As you are aware, I have laid out three key priorities that I believe will position Illumina for accelerated growth and profitability as market conditions improve. My first priority, driving our top line, is centered on continuing to grow our installed base and helping customers accelerate utilization of these instruments in new and existing applications. I discussed earlier how pleased we are with the first year of NovaSeq X shipments. For high throughput, more broadly, across the NovaSeq X and NovaSeq 6000, we placed more than 400 instruments in 2023. In 2024, we will support this growing installed base as customers launch large projects and more sequencing-intensive applications like multiomics, liquid biopsy, and minimal residual disease, or MRD. We anticipate ongoing high-throughput instrument orders throughout 2024, primarily coming from further conversion of NovaSeq 6000 customers to the X, from customer fleet expansions, and long term, from new to high-throughput customers. With that said, given the significant number of placements in 2023, we believe we will ultimately ship fewer high-throughput instruments in 2024. As you are aware, XLEAP- SBS chemistry has been the engine for our X platform, delivering significant improvements in quality, turnaround time, and cost. This quarter, we'll be making XLEAP available to our mid-throughput customers on their existing NextSeq 1K, 2K instruments without having to upgrade their instruments. This offering will further strengthen our leadership position around the world and drive progress in markets such as single-cell, spatial, and proteomics. As we grow installed base, we will remain focused on supporting our customers as they launch new projects. This will build momentum for consumables demand this year and going forward. Already, our efforts to develop this demand is paying off. In Q4, we saw higher than expected growth in X consumable sales following the late October launch of our much-anticipated 25B read kit. More recently, in January, we launched a 1.5B kit, which together with the 25B and the 10B flow cells, allows us to offer a full suite of products to the NovaSeq X customers. While we will continue to see customers reduce their inventories of NovaSeq 6000 consumables as they transition to the X, building pull-through on the NovaSeq X will drive our overall high-throughput consumables growth this year. Turning to my second priority, I'm focused on delivering operational excellence by applying greater rigor throughout our P&L, while sustaining innovation and growth. We have launched a multi-year effort focusing on improving our margins through greater productivity and pursuing additional areas for cost savings. In January, we took an additional action to further optimize our global workforce. Over the past year, we have made cumulative role reductions totaling approximately 12%. Our most recent actions included an adjustment that we aligned with our late 2023 portfolio optimization efforts. You'll see us continue to take steps to not only manage our near-term cost, but also to build our agility to deliver more sustained growth and margins over time. Illumina is taking a highly disciplined approach to support our customers, employees, and partners, and to deliver shareholder returns throughout a range of macroeconomic environments. Moving to my third priority, which is working to resolve GRAIL as quick as possible. Since joining Illumina, I've made it an imperative to move with speed on GRAIL. In December, we announced that we would divest GRAIL with a goal of finalizing the terms of a transaction by the end of the second quarter this year. We'll continue to pursue parallel paths. The divestiture will be executed through a third-party sale or capital markets transaction, consistent with the European Commission's divestiture order. To date, we've been able to make swift progress. GRAIL's Form 10 has been confidentially filed with the SEC. Our advisers are actively moving the process forward on both sale and capital markets paths. The special committee of the board that we established in Q3 continues to help ensure this process moves forward efficiently. I'm encouraged by the momentum we've entered 2024 with, and I'm committed to seeing our initiative through. For now, I will ask Joydeep to share more detail on our results for 2023 and our outlook for 2024. Thank you, Jacob. I'll start by reviewing our consolidated financial results, followed by segment results for Core Illumina and GRAIL, and then conclude with my remarks on our current outlook for 2024. I'll be discussing non-GAAP results, which include stock-based compensation. I encourage you to review the GAAP reconciliation of these non-GAAP measures, which can be found in today's release and in the supplementary data available on our website. In the fourth quarter, consolidated revenue of $1.12 billion was up 4% year over year, both on a reported and constant currency basis. Consolidated revenue was flat from the third quarter of 2023. Non-GAAP net income was $22 million, or $0.14 per diluted share, which included dilution from GRAIL's non-GAAP operating loss of $152 million for the quarter. Non-GAAP EPS exceeded our expectations, driven by higher revenue and gross margin and lower operating expense for the quarter. Our non-GAAP tax rate was 55.4% for the quarter and 41.8% for full year 2023, compared to 29.3% in Q4 2022, and 26% for full year 2022. Although both periods reflect the impact of R&D capitalization requirements, the impact to our effective tax rate in 2023 was more significant due to our lower earnings. In addition, our non-GAAP tax rate for both years include a meaningful impact from the consolidation of GRAIL's losses. Absent the impact of GRAIL, our full year 2023 core tax rate was in the mid-twenties. Our non-GAAP weighted average diluted share count for the quarter was approximately 159 million. Moving to segment results. Core Illumina fourth quarter revenue of $1.1 billion was up 3% year-over-year on both a reported and constant currency basis, and included an anticipated reduction of approximately 5 percentage points from two primary categories. One, the decrease in COVID surveillance and the effect of sanctions in Russia, that together represented approximately 3 percentage points. And two, the year-over-year reduction in China revenue that represented approximately 2 percentage points. Despite these impacts, core Illumina revenue exceeded expectations due to stronger than projected NovaSeq X placements and uptake in X consumables, with strong early demand for the 25B flow cell that launched in Q4. Core Illumina sequencing consumables revenue of $687 million was flat year-over-year. Stronger than expected NovaSeq X consumables purchases were largely offset by the anticipated reduction in NovaSeq 6000 consumables and the impact of pricing transitions, as customers continue to adopt the NovaSeq X. Total sequencing consumables revenue was also impacted by COVID, Russia, and China factors that I previously noted, as well as the continued impact of macroeconomic conditions on customers' purchasing behavior. COVID surveillance contributed approximately $4 million in total revenue in Q4 2023, compared to $20 million in Q4 2022. Turning to sequencing activity, total activity on our connected high and mid-throughput instruments grew 46% year-over-year in the quarter, following the 29% year-over-year growth we reported in Q3. Sequentially, Q4 sequencing activity grew 13% from Q3. As a reminder, we believe this data is a useful reference that shows the general activity trends across our installed base and is directionally correlated with revenue over time. Sequencing instruments revenue for Core Illumina of $161 million grew 10% year-over-year in Q4, driven primarily by NovaSeq X, which more than offset the decline in NovaSeq 6000 shipments. Growth in high-throughput instruments was partially offset by the expected decline in mid- and low-throughput shipments due to capital purchase and cash flow constraints that continue to impact our customers' purchasing behaviors, as well as local competition in China. For NovaSeq X, we exited Q4 with 390 orders since launch. Our shipments of 79 NovaSeq X instruments in Q4 brought our total installed base to 352 instruments. While we expect most of our NovaSeq 6000 customers to transition to the NovaSeq X over time, we are still very early in this transition. As of the end of 2023, our net install base for NovaSeq 6000 was approximately 1,770 instruments, which reflects approximately 110 instruments that have been deactivated between 2017 and 2023. The majority of these were in 2023 due to customer transitions to NovaSeq X. We expect this to increase in 2024 as customers continue to ramp up utilization of NovaSeq X. Additionally, going forward, we will be reporting our annual instrument install base figures on a net basis, which accounts for instruments that have been decommissioned or inactivated since launch. The information included on this slide includes additional details to help you with your modeling. We will be posting this presentation to our investor relations website following our prepared remarks. Core Illumina sequencing service and other revenue of $152 million was up 16% year-over-year, driven primarily by an increase in revenue from strategic partnerships and higher instrument service contract revenue on a growing installed base. Moving to the rest of Core Illumina P&L. Core Illumina Non-GAAP gross margin of 64.7% for the quarter decreased 260 basis points year-over-year, primarily driven by the mix of lower margin strategic partnership revenue, lower instrument margins due to the NovaSeq X launch, which is typical with a new platform introduction, and increased field services and installation costs, partially offset by lower freight costs. Core Illumina non-GAAP operating expenses of $507 million were down $21 million year over year, primarily due to continued expense reduction initiatives and lower performance-based stock compensation expense year over year. As a result of these factors and higher revenue, core Illumina non-GAAP operating margin was 18.5% in Q4 2023, compared to 17.8% in Q4 2022. Transitioning to financial results for GRAIL. GRAIL revenue of $30 million for the quarter grew 30% year-over-year, driven primarily by adoption of Galleri. GRAIL non-GAAP operating expenses totaled $167 million, and increased $1 million year-over-year. Moving to consolidated cash flow and balance sheet items for the quarter. Cash flow provided by operations was $224 million. Capital expenditures were $51 million, and free cash flow was $173 million. We did not repurchase any common stock. We ended the quarter with approximately $1.05 billion in cash, cash equivalents, and short-term investments. Moving now to 2024 guidance. As Illumina continues to move as quickly as possible to resolve GRAIL, given the uncertainty around the specific timing and impact of the GRAIL divestment, the company is focusing its 2024 financial outlook on core Illumina. Our guidance does not assume any impact for the potential divestment of GRAIL in 2024. Upon the completion of the divestment, we will provide non-GAAP EPS guidance for the full year 2024. As Jacob mentioned, our outlook assumes the current challenging macroeconomic environment persists in 2024, and tighter funding and budget pressures continue to impact our customers' purchasing decisions. We expect full year 2024 core revenue to be approximately flat from 2023, reflecting the following offsetting factors: We expect core Illumina sequencing instrument revenue to decline in the high teens year over year, driven primarily by a decrease in NovaSeq X instrument placements. The reduction reflects the expected transition in our adoption curve to early majority customers from early adopters and a lower backlog entering 2024 compared to 2023. We also expect capital and cash flow constraints to continue to impact purchasing behavior and moderate instrument placements in 2024. We expect core Illumina sequencing consumables revenue to grow in the low single digits year over year, driven primarily by modest growth in high-throughput consumables, as increased NovaSeq X consumables purchases and sequencing volume outpace the expected decline in NovaSeq 6000 consumables and the impact of pricing transitions. Moving to annual pull-through. Going forward, we will be calculating and providing pull-through figures based on the instrument's net install base. As I mentioned previously, supplemental information is included in our earnings presentation to help with modeling, which will be posted to our investor relations website following our prepared remarks. Importantly, this does not change reported revenue in any way. We expect annual pull-through for NovaSeq 6000 of approximately $700,000-$800,000 per system in 2024, as customers continue to transition sequencing volume to NovaSeq X. We expect annual pull-through for NextSeq 1K/2K in the range of $80,000-$130,000 per system in 2024, which primarily reflects the impact of customers transitioning to XLEAP chemistry as it becomes available on NextSeq 1K/2K. We expect annual pull-through for MiSeq in the range of $30,000-$40,000. We expect the remainder of our pull-through ranges to be in line with historical guidance. We expect core Illumina total sequencing revenue to be approximately flat year-over-year. This includes intercompany sales to GRAIL of approximately $30 million, which are eliminated in consolidation. We expect core Illumina non-GAAP operating margin of approximately 20%. Our operating margin expectations reflect the benefit of our continued gross margin improvement and expense reduction initiatives, offset by normalization of our performance-based compensation, as well as the impacts of inflation and market-based merit increases. For the first quarter of 2024, we expect core Illumina revenue in the range of $1.03 billion-$1.04 billion, reflecting a year-over-year decrease of 3.5%-4.5%, driven predominantly by the following factors: We expect lower NovaSeq X instrument shipments year-over-year, given that we are entering 2024 with a more modest backlog compared to the significant pre-order book we entered 2023 following the launch of NovaSeq X. We expect the increase in NovaSeq X consumables purchases year-over-year to be largely offset by the anticipated reduction in NovaSeq 6000 consumables and the impact of pricing transitions, consistent with the trend we saw in Q4. We expect an increase in sequencing service and other revenue year over year, driven by strategic partnership initiatives and higher instrument service contract revenue on a growing installed base. For the first quarter, we expect core Illumina non-GAAP operating margin of approximately 18%. Lastly, for the first quarter, we expect core Illumina non-GAAP net other expense of approximately $12 million, with the year-over-year increase driven primarily by lower interest income on our lower cash balance following the repayment of our convertible notes in mid-2023. I will now turn it back over to Jacob for his closing remarks. Thank you. Thanks, Joydeep. Before we close and move to Q&A, I want to discuss what I believe success looks like, both this year and the years ahead... Illumina has the opportunity to truly drive the next-generation sequencing ecosystem forward. We will deepen our relationships with our customers and seek out greater ways to collaborate and partner with them to drive greater adoption of NGS. Our goal is to make our customers the heroes in their labs, and to support them as they expand their work in genomics and multiomics. In turn, this will help capitalize our market-leading innovation and continue to differentiate Illumina and maintain our industry-leading position across research and clinical markets. We will also continue to drive innovation that is focused on our customers' priorities. This include involving our sequencing platform and delivering greater sample-to-answer solutions. There is an opportunity to further integrate customers' workflow to build our share of wallet as we create greater value for our customers. Our comprehensive strategy work is well underway, and we will share more with you later this year. I'm excited to be part of Illumina's leadership team that is driving our unmatched core business forward. Thank you for joining. I'll now invite the operator to open the line for Q&A. Thank you. If you would like to signal with questions, please press star one on your touchtone telephone. If you're joining us today using a speakerphone, please make sure your mute function is turned off to allow your signal to reach our equipment. As a reminder, please limit yourself to one question so that we can accommodate as many analysts as possible. You're welcome to reenter the queue if you have additional questions. Again, that is star one to signal with questions, star one. Our first question will come from Doug Schenkel with Wolfe Research. Hey, good afternoon, everybody, and thank you for taking the questions. I want to ask just about the 25 B, 25 B chip release and what you're seeing in the field entering the early part of the year. As you know, 25 B reduces the cost per genome to about $200, but it also requires customers to have enough samples to run to fully use up the flow cells. So what have you seen in the first few months of availability? You know, what's spending on X consumables? You know, how does that trend relative to Q3? And are you seeing signs in the field that sample access is not a problem, you know, as you see folks move to the 25 B? Thank you. Thanks, Doug, and, no, that was a nice one question there. So let me start by saying that we've been very pleased with the pickup of the 25B since the launch in late November. In fact, it kind of performed over our expectations, and have been very well received with our customers. So we continue to expect that this will continue to really drive the X performance, but also, of course, it completely now unleashed the full performance of the instrument, and thereby, we also expect that the 25B, the availability of the 25B will have more customers to jump onto the X wagon here. I think we are seeing customers being able to load it. Of course, many of them are still doing validation work, but we are seeing that they have big enough projects to load this flow cells. Yeah, and just maybe one quick add, right? About 40% of our X customers so far have adopted the 25B. Correct. Our next question will come from Puneet Souda with Leerink Partners. Yeah, hi, Jacob. Jo, thanks for taking the question. So, maybe just following up on that point, I mean, sort of help us just understand how do you get to the low single-digit, you know, growth rate this year? There's obviously 25B, there's reductions that are happening from just the X installs, cost per gigabase is lower, China continues to be challenging, and then the market backdrop is challenging too. So just maybe talk to us a little bit about sort of how do you, you know, continue to have confidence in the sort of a low single-digit, you know, sequencing consumable growth rate. And I would really appreciate if you could provide us some context around, and details around GRAIL as well. What's the progress there? Any level of interest that you're finding, and what are you contemplating for spend on GRAIL this year? Thank you so much. All right. Thanks for that, Puneet. And let me start by the latter part of this question about GRAIL, and then I will have Joydeep chime in on our expectations here on consumable growth. But as I mentioned, you know, we are very pleased with the announcement that we made here in December that we're now divesting GRAIL for sure. And I'm actually very pleased with the progress so far. We have our advisors really moving ahead and are in connection and in conversations with relevant parties. We are continuing to run a dual track, of course, via a capital market initiative, or it can be a transaction. And so, we still expect to be on track with the timeline we were previously talking about, that we will have all the terms finalized by end of Q2. So we are, at this point, not talking about the, since we are expecting to finish up with GRAIL this year, we're not having any guidance on the expenditure for GRAIL this year. Yeah, and to address your question about the low single digits consumables growth, Puneet. So, you know, let me start by saying we were very encouraged by the uptake of the 25B and 10B flow cells that we saw in the fourth quarter. We're also very pleased to see the elasticity, the growth in underlying sequencing activity being driven by X customers, right? So both of those are good. We saw that uptick on sequencing activity now for the second quarter in a row. So again, it's broad-based, it's both research and clinical customers, and it's quarter-on-quarter and year-on-year growth. So what's offsetting that, you know, expected growth in X consumables, as you rightly pointed out, is the expected price transition as customers move from the NovaSeq 6000 to the X. This is very similar to the price transition that you saw when you were moving from HiSeq to Six K. And then, of course, some of the expected, again, reduction in Six K consumables as customers switch from one platform to the other, right? So that is the really big piece on, you know, what's leading to the lower, or the low single-digit growth rate in consumables in 2024. Our next question will come from Vijay Kumar with Evercore ISI. Hey, guys. Thanks for taking my question. I had a two-part question. On this, GRAIL, I know it was a confidential S-1. When will it be made public? The reason I ask is that GRAIL's operating losses were $700 million last year. It's really hard to foresee a capital market transaction with those kind of spend levels. So I'll be very curious to see what the S-1 assumptions are on GRAIL. And on consumable pull-through, $700,000-$800,000 on NovaSeq 6000. Joydeep, is there like a cadence, perhaps Q1, we're starting at the low end, and is the assumption we exit Q4 at the high end of that range? Yeah, so let's start with the GRAIL question, and obviously, we'd like to provide as much information to all of you as possible. Right now, as you say, the filing is confidential, and I don't think it'll be publicly available before very late in Q1, maybe dripping into Q2 here. So I think that's where we are at this. But as soon as it's available, we make sure you know. Okay, and then, Vijay, I want to be sure, you were—you're asking about NextSeq six thousand—sorry, NovaSeq 6000, pull-through numbers and how they modulate through the year? Correct, Joydeep. Is there an assumption we start at the low end and exit the year at the high end or above the high end of the range? No, there isn't. I think, again, pull-through, I will reemphasize, is a calculated number, so it's more of, you know, the total amount of consumables, sold in any quarter, divided by, you know, the number of, now the active install base in, in the, in the quarter, right? So, and we don't have an assumption in terms of, quarterly spread on that. Our next question will come from Dan Arias with Stifel. Hey, guys. Thanks for the questions. Jacob or Joydeep, on the 6000 to X transition, and just sort of thinking about the clinical side of things, you know, a big part of that bucket are these commercial labs that are watching their own margins pretty tightly and trying to find ways to be just more efficient. So are you sensing that maybe you could see X adoption faster than in, maybe in a normal environment, in order for those folks to take advantage of the cost savings? It seems like they're incentivized to do that, but I also know that the clinical wheel spins slowly, so I'm just not sure whether that's a factor for them. Yeah, of course, it's a relevant hypothesis to come in with. What we have seen is that most of our clinical customers are using the opportunity with the lower cost on X to actually expand and the depth of sequencing, providing bigger panels and so on. So what we are seeing is that most of the current panels continue to run on the NovaSeq 6000, and thereby continue to also drive volume there. And then they are right now validating many of the newer assays or the new assays that might not have been possible in the 6000 due to the cost and so on, to be on the X. So we're quite encouraged about that. We've also seen several of our specialty labs customer now order tens of NovaSeq X. So I'm encouraged that we will see a lot of volume here going forward on this. Our next question will come from Subbu Nambi with Guggenheim Securities. Hey, thank you, guys. Thank you for taking the questions. You spent about $1 billion on R&D in 2023. Relative to 2019, your revenue has grown at 6% CAGR; however, R&D has grown 12% CAGR. Why can't you reduce R&D spend in dollar terms from current levels over the next 1 or 2 years? Can you outline where the spend is allocating? Yeah, thank you. You're right that we continue to believe that there's a lot of innovation that is required, and thereby investment into R&D in order to drive the whole NGS ecosystem forward. As I said, one of the things—what I said previously is one of the things that I was really excited about is the pipeline of innovation that we have running right now, and thereby also that will be a lot of innovation coming out from Illumina over the next period of time here. And we continue to believe that we are in the early stages of the whole opportunities here in NGS, but even also multiomics, and thereby, we continue to make investment into that. You're also right that there has been an increase in R&D, and we certainly looking to change that trajectory over time. We still believe that a high level of investment is required, but you will see here over the next year that the percentage spending on R&D versus revenue will start to come down. Just to add, Subbu, I think we have made reductions in R&D over the last year. It's been very strategic in terms of specific aspects of the portfolio that we had considered as longer, much longer payoff time of payoffs or more risky. And we've also our overall R&D includes spend in certain areas like medical affairs, et cetera, that we were doing to support customers. And as they have matured, right, we have been able to pull back on investment there without affecting innovation. Yeah. Good. We'll take a question from Mason Carrico with Stephens. Hey, guys. Thanks for the question. So for high-throughput customers who have already purchased the Next, could you talk about the conversations you're having around the potential fleet expansions? I mean, what portion of those opportunities, whether it's orders or shipments, have already come through, and how many, you know, remain an opportunity this year? Yeah, I think, I mean, we certainly see a lot of our high-end customers or high-volume customers that started buying one or two NovaSeq X, is starting to consider purchasing more instruments. So they're using the first few X to validate assays on, and then they wanna expand into, into, you know, use the additional X's to actually run in production. But very few customers have still gone into production mode, and thereby, there is a real big opportunity in front of us. I think that less than half of our high-volume customers have purchased an X so far, so I think there's still a lot of opportunities there. But as also mentioned, some of the high-volume customers that have purchased one or two have now put orders in for 10 instruments. So, I think we still in the very early stages, and there should be a lot of opportunities here, both in 2024 and 2025, to drive more placements. Yeah, and just to add, we weren't expecting to see that before the launch of the 25B flow cell, right? So really, you're in very early innings there, and we do expect to see those fleet expansions come in in this year. We have a question from David Westenberg with Piper Sandler. Hi, thank you for taking the question. I'm actually gonna hit on some of the competition coming in. A couple different things, we saw at AGBT, for example, a combination of spatial and sequencing on one platform. How do you see that stacking competitively? Would you pursue a strategy like that? And then on Ultima and the $100 genome, you know, some of the specs look significantly better than it did a couple of years ago. You know, how do you feel stacked up against the $100 price and, you know, with some of your key bells and whistles? Thank you very much. Yeah, thanks, Dave. And of course, we're tracking of course everything that is happening on the market, and we take our competition very seriously. But I think you've also heard me on the multiomics place. I think you've heard me speak multiple times about multiomics, so we have an intention also to be in that space. I think we've been out talking about moving forward as a starting point with proteomics here, with our relationships with SomaLogic. But I think you can see that. Actually, we believe there is many more modalities that can be available on the instrument. So, I think where Illumina is doing is that we will go out and provide that insight when we're ready to put something in the market and speak less about it when it's more in the future. Secondly, you know, we feel with the NovaSeq X, where we come out with a very attractive price point for a lot of different applications and not only a very few ones. So I think we are—we feel that we have a very attractive solution. But I also remind you that it's not only the cost per sequencing that anymore that is relevant, but also you need to look at the whole cost of the whole workflow, how many manual steps you have, how much waste you are is the instrument spending and so on. So I think if you dig into the details, you will actually realize that Illumina has a very attractive and very differentiated platform. And we'll take a question from Conor McNamara with RBC. Hey, guys, and thanks for taking the questions. Appreciate it. Just a financial question on margins. You got into 18% in Q1 and 20% for the whole year. So how do we think about the cadence of the margin progression? And I guess same on tax rate, just you talked about a mid-20s% for the core Illumina tax rate. How should we think about that in 2024? Yeah, so the tax rate, again, you know, is something that you should expect to be, you know, relatively constant as you go into and, again, for core Illumina into 2024. And this is again, core Illumina, right? We are not giving guidance this year yet on the consolidated number. In terms of the operating margin cadence, again, you know, that is typically does go up, you know, as the gross margins tend to go up as we move into greater volume and through the year. In terms of operating margin, you will see a decrease in potentially in Q2 as the merit and the other, you know, inflation-related aspects come into play. But then you will see after that, a quarter-on-quarter increase as we move into the rest of the year. And we'll- Yeah, and then, of course, you know, I think on, on the—sorry, just, just one other thing, right? I know there's been some movement in terms of the R&D capitalization piece, but, you know, that is something we're monitoring very carefully. It has passed the House, but it still needs to get through the Senate and the President signing. If we get that, you can expect a further improvement in the tax rate, right? But we are not building that into our assumptions at this point. Our next question will come from Sung Ji Nam with Scotiabank. Hi, thanks for taking the question. Just on the MRD assay under development with Janssen, was wondering if you might be able to comment whether that's a tumor-informed or tumor-naive approach, or something different altogether, and whether there might be potential for that to be developed into an IVD assay in the future for clinical applications. Thank you. Yeah, thanks for the question. So again, to remind everyone, the approach that Illumina has is quite unique. It's a whole genome-based MRD assay. You know, it is initially a tumor-informed assay, but it does have the potential with more data and you know, behind it to at some point move into a tumor-naive, right? In terms of being you know, capable of being IVD, of course, as you know, we have invested very heavily in platforms and technologies and infrastructure that allow us to move assays to be IVD when the time is right, right? So right now, the agreement we have with pharma has been mainly to explore this in various forms, but we can go move into IVD when the time is right. Well, let me also add that we have no intention of providing that through a CLIA lab, a commercial CLIA lab. We do have our CLIA lab that, of course, is running very few samples, but we're not going out and commercialize it through our CLIA lab. In fact, we are very interested to work with customers and partners to continue to develop this. We'll take our next question from Patrick Donnelly with Citi. Hey, guys. Thanks for taking the questions. Joydeep, maybe a quick one for you, and the follow-up would be probably more for Jacob. But just on the gross margin piece, can you talk about, you know, a Q4 step down a little bit, came in a little light where we were. Can you just talk about anything that impacted that Q4, the right way to think about the progression there throughout 2024? And then on the gross margin kind of pricing initiatives, Jacob, how are you thinking about just the price side? Again, I know someone mentioned AGBT competitors are making noise and saying they're seeing discounting in the market, particularly on kind of the mid-throughput side. So just curious, as you've taken a look here, you know, what you're thinking about on the pricing side. Thanks, guys. Yeah. So, Patrick, in terms of, you know, sequential decrease in fourth quarter on gross margin, you know, there are several factors there, right? One, revenue was lower, so that has an impact, obviously, in terms of, you know, just absorption of fixed costs. We also did have a higher than expected contribution, and that coupled with more of the partnership revenue, which tends to be lower margin-driven, all affected our gross margin numbers. And then lastly, I will say there was a mix shift from 6K consumables to X consumables, and that also had an impact in our overall gross margin number for Q4. I will say, and I think it leads into, you know, your question to Jacob, we have made a lot of progress in 2023 in terms of COGS productivity, and we started seeing the benefits of that as we rolled out of 2023 and into 2024 as well and beyond. Yeah, when coming into the company here, Patrick, and looking into pricing and how we are thinking about pricing going forward, first, I will say that Illumina is presenting a premium product, and thereby, I think also our customers are seeing that we can command a premium pricing in the industry. But I think more importantly is that only talking about cost per gigabase is probably too simplistic for most of our customers. They are more interested in the cost for the whole, for Sample to Insight, for the whole workflows. And that is, of course, including sample prep automation, but probably even more importantly, informatics, which is also a key cost driver for our customers. So really, with the DRAGEN platform, and what we have in our comprehensive informatics offering, we actually can provide the customer with a very cost attractive solution. So therefore, it, the thing about just talking cost per gigabase is kind of maybe the old way of looking at it, and the future way we look at it a little more comprehensive. So I feel really good about that, where we are. And that said, we will now, with, in the mid-throughput, with the XLEAP- SBS chemistry be available. We are coming out with a more attractive pricing, quality and more capacity on our 1K and 2K instruments. So I'm really excited about that, and again, driving elasticity based on that new price point. So you will see us really move the knobs on many more elements than just one pricing element. Our next question comes from Eve Burstein with Bernstein Research. Hi there. Thanks a lot for taking the question. Wanted to ask about NextSeq placement. So there, you ended the year with 885 placements, and that's comfortably above where you were pre-pandemic, but it's also below where you've been for the last two years. So how much of this do you attribute to just, you know, changing needs, obviously, post-pandemic? How much do you attribute to the capital purchase and cash flow constraints that you talked about? And how much do you attribute to competitive dynamics, which you also talked about? And then how should we think about what normalized demand here looks like going forward? Yeah, so I think the major factors, I would put two, maybe three, right? And then, there's a sub-factor. So the major factors, as you rightly pointed out, you know, coming out of COVID, in '21 and '22, we had a real uptick in the amount of mid-throughput instruments and low- throughput instrument sales, right? And that has normalized a little bit as, you know, the COVID threat, thankfully, has reduced. We also, at the same time, did see in 2023, some of the macroeconomic conditions that led to more conservatism at our customers and, you know, more conservatism in the purchases on capital come through. The third factor in mid-throughput especially, was also China, right? So if you're looking at an overall number, we did get impacted in China, for competition and for macroeconomic reasons, as we have repeatedly stated in our 2023 earnings calls. As far as competition goes, I mean, clearly that was a factor in China, but that does not seem to be a huge factor in the rest of the world, right? And we did see our. You know, we track our competitive win rates fairly closely, and we did see that stabilizing in Q3 and in Q4. Moving on to Dan Brennan with TD Cowen. Great, thanks for the questions, guys. On the X pull-through, you know, we would come out with around $1 million in the fourth quarter, and some quick math, we arrive at something like maybe $850,000 in 2024. So any comment on those numbers, if they seem reasonable, and if so, could you just speak to, like, what would drive, you know, the assumption for that kind of, you know, kind of sequential step down? Thank you. Thanks, Dan. I think you've done more math than that we have at this point, since it's still way too early in the way early innings here to start to look at pull-through from the X. So we haven't really done that math as of yet, and we will provide that math when we think we are more in a stable situation where it makes sense. Any other comments on that, Joydeep? No, I think, you know, I'll reiterate. Look, it is early. I think Jacob stated earlier that many customers are just going through validation, especially on the 25B. So, I will disagree with him that we haven't done the math, but the math is not relevant, and we don't want to confuse you. When this stabilizes, right, we will absolutely come out with a number, but so far what we have seen has been encouraging to us. We have a question from Dan Leonard with UBS. Thank you. Jacob, I'm curious if you could elaborate further on the health of your diagnostics markets following your customer listening tour. And with looming FDA regulation of LDTs, how does that impact demand for your products or not? Yeah, no, I think that's a good question, and something also I, I really was eager to understand better coming into Illumina. As, as you know, I have a background in IVD, and I have a lot of passion for, for cancer diagnostic, but really fighting cancers. And I think how we, how we think about it, of course, that we serve a lot of clinical customers out there that is using the Illumina ecosystem and, and build, build companies on top of that, primarily into the LDT space. And then we have our own offerings in other LDT, but in other place also IVD on, especially the TSO 500 and the NIPT and other places where... And if you look into our TSO 500 business, it's been growing really fast over the last period of time, and it's more than $100 million now, and we expect to have high double-digit growth also into this year, and we don't see any end to that right now. So I'm really, I'm really bullish around where we can bring that, and we are, of course, looking into a strategic review right now on how does that fit into the overall, you know, core business strategy. But clearly, we would also like to play in that space going forward. Was there another? Was there a second part of that question? Regulation impact. Yeah. Okay, so I think the second part was the impact of the reregulation. I mean, of course, we're monitoring that very, very deeply right now, and there's of course, again, a conversation with our customers, and we're helping some customers make sure they're ready for that. The larger customers can, of course, go through a single-site PMA, which helps them. But there's also a changes maybe in the leveling of the different clinical, so some of the Class III products are considered being brought down to Class II products right now. It's not. It's still kind of on the table for consideration, but if that happens, that will certainly also reduce the requirements for getting through clinical trials and so on. So I think there's still a lot of moving elements, but what I can tell you is that I think Illumina is very well positioned to support the markets going forward, almost independent on where FDA is landing on this one. Yeah, I'll just add, Jacob, that, you know, we are about the only company that has, even in our RUO products, ISO 13485 classification on all our, our instruments and, and in most of our consumables, and we have obviously the path to IVD should our customers want it, right? So we're well, well-positioned to serve whichever direction they want to go in. Our next question will come from Kyle Mikson with Canaccord. Yeah, thanks for the questions. Just following guidance. So, it seems like you probably had the opportunity to kind of establish an outlook that was softer than what you said in November. Could have set a low bar. You kept the range, though, risks clearly remain. How much like visibility or confidence do you have, and how much conservatism are you kind of baking in compared to prior years? And you listed some, but what are the most material swing factors and kind of risks that we should consider in one Q and then first half or second half? And if I could just ask one for you, Joydeep, on 6,000 pull-through. The $700,000-$800,000 seems like possibly aggressive compared to how I see kind of decline in its years post the 6,000 launch. So just kind of walk through what you're thinking about in terms of the decline, I guess, or deterioration in 6,000 pull-through. Thanks. Let me address the 6,000 piece first. It may be an easier one, right? So remember when HiSeq was, well, NovaSeq 6000 was introduced, we didn't have as many clinical customers, right? So now we have clinical, about, you know, about 50% of our, our cons revenue is coming from clinical customers, who have these validated assays, right? Where you, you're not gonna change platforms in the short term. So, the overall reduction in pull-through will be more mitigated compared to what you saw with HiSeq. You know, Jacob, you want to comment on the overall guidance, or you want me to? No, you can continue. Okay. So I think overall, look, we have repeatedly said, right, we see this as a prudent approach to the overall forecast, right? And you know, while there have been some signs in some markets that the macroeconomic conditions might be turning, we have not assumed this in our forecast. And you know, the only place we have been pessimistic, and of course, has been in China, right? Where you know, the recent news also seems to corroborate that piece. As far as the puts and takes, look, it's a lot about adoption of the X, right? So, we're spending an inordinate amount of time making sure that our X customers can transition quickly, can adopt and get on with their assays as quickly as possible, and we will continue to do that. And of course, if the markets pick up, we are very well positioned then to benefit from any of the upsides. On the flip side, it's, you know, it, further macroeconomic headwinds that further reduce our customers' ability to bring on the X or to spend on consumables will affect us as well. Jacob, I don't know if there's anything else you want to add. Good. I think we're good. Our next question will come from Rachel Vatnsdal with JP Morgan. Great, good afternoon, and thanks for taking the questions. I just want to follow up to your answer on Patrick's question earlier. You mentioned that the gross margin line in Q4 was lighter due to that consumables mix shift from 6000 to the X. So can you just walk us through that dynamic a little bit more? Is this just a function of the X's ramping, so there's less volume leverage at this point, or is there something where X consumables are structurally lower margin? And then how should we think about that consumables mix impacting gross margin throughout 2024 as well? Yeah. So, first easy part is, you know, no, we have-- we have said, right, all through, right, that we had designed the, the X and X consumables that at scale, right, they would... we would expect the margins to be comparable to, to X consumables at scale. What you're seeing is, of course, early on in the, in the adoption, you're gonna see the, the consumables, margins be lower. We haven't fully scaled up, and as we move through 2024, you will see that, you know, more or less normalized. Now, as you go into 2024, overall gross margins will be, you know, have, several factors, right? So one, we will have a little bit of a benefit from, from the, from this, lower placement of instruments. As you said, we've said, right, that we do expect that to decline. So a little bit more consumables that will lead to an increase in gross margin. We also will benefit from, you know, some uptick in terms of all the actions we have taken to improve COGS productivity. So those are the two largest things that will serve to improve our gross margins as we get into 2024. Thank you. That concludes our Q&A session. I will now hand the call back over to Salli Schwartz. Thank you for joining us today. As a reminder, a replay of this call will be available in the Investors section of our website. This concludes our call, and we look forward to seeing you at upcoming conferences and other events. Thank you. That does conclude today's conference. We do thank you for your participation and have an excellent day.