Introduction – Company Background

GuangXin Industrial Co., Ltd. is a specialized manufacturer dedicated to the development and production of high-quality insoles.

With a strong foundation in material science and footwear ergonomics, we serve as a trusted partner for global brands seeking reliable insole solutions that combine comfort, functionality, and design.

With years of experience in insole production and OEM/ODM services, GuangXin has successfully supported a wide range of clients across various industries—including sportswear, health & wellness, orthopedic care, and daily footwear.

From initial prototyping to mass production, we provide comprehensive support tailored to each client’s market and application needs.

At GuangXin, we are committed to quality, innovation, and sustainable development. Every insole we produce reflects our dedication to precision craftsmanship, forward-thinking design, and ESG-driven practices.

By integrating eco-friendly materials, clean production processes, and responsible sourcing, we help our partners meet both market demand and environmental goals.

Core Strengths in Insole Manufacturing

At GuangXin Industrial, our core strength lies in our deep expertise and versatility in insole and pillow manufacturing. We specialize in working with a wide range of materials, including PU (polyurethane), natural latex, and advanced graphene composites, to develop insoles and pillows that meet diverse performance, comfort, and health-support needs.

Whether it's cushioning, support, breathability, or antibacterial function, we tailor material selection to the exact requirements of each project-whether for foot wellness or ergonomic sleep products.

We provide end-to-end manufacturing capabilities under one roof—covering every stage from material sourcing and foaming, to precision molding, lamination, cutting, sewing, and strict quality control. This full-process control not only ensures product consistency and durability, but also allows for faster lead times and better customization flexibility.

With our flexible production capacity, we accommodate both small batch custom orders and high-volume mass production with equal efficiency. Whether you're a startup launching your first insole or pillow line, or a global brand scaling up to meet market demand, GuangXin is equipped to deliver reliable OEM/ODM solutions that grow with your business.

Customization & OEM/ODM Flexibility

GuangXin offers exceptional flexibility in customization and OEM/ODM services, empowering our partners to create insole products that truly align with their brand identity and target market. We develop insoles tailored to specific foot shapes, end-user needs, and regional market preferences, ensuring optimal fit and functionality.

Our team supports comprehensive branding solutions, including logo printing, custom packaging, and product integration support for marketing campaigns. Whether you're launching a new product line or upgrading an existing one, we help your vision come to life with attention to detail and consistent brand presentation.

With fast prototyping services and efficient lead times, GuangXin helps reduce your time-to-market and respond quickly to evolving trends or seasonal demands. From concept to final production, we offer agile support that keeps you ahead of the competition.

Quality Assurance & Certifications

Quality is at the heart of everything we do. GuangXin implements a rigorous quality control system at every stage of production—ensuring that each insole meets the highest standards of consistency, comfort, and durability.

We provide a variety of in-house and third-party testing options, including antibacterial performance, odor control, durability testing, and eco-safety verification, to meet the specific needs of our clients and markets.

Our products are fully compliant with international safety and environmental standards, such as REACH, RoHS, and other applicable export regulations. This ensures seamless entry into global markets while supporting your ESG and product safety commitments.

ESG-Oriented Sustainable Production

At GuangXin Industrial, we are committed to integrating ESG (Environmental, Social, and Governance) values into every step of our manufacturing process. We actively pursue eco-conscious practices by utilizing eco-friendly materials and adopting low-carbon production methods to reduce environmental impact.

To support circular economy goals, we offer recycled and upcycled material options, including innovative applications such as recycled glass and repurposed LCD panel glass. These materials are processed using advanced techniques to retain performance while reducing waste—contributing to a more sustainable supply chain.

We also work closely with our partners to support their ESG compliance and sustainability reporting needs, providing documentation, traceability, and material data upon request. Whether you're aiming to meet corporate sustainability targets or align with global green regulations, GuangXin is your trusted manufacturing ally in building a better, greener future.

Let’s Build Your Next Insole Success Together

Looking for a reliable insole manufacturing partner that understands customization, quality, and flexibility? GuangXin Industrial Co., Ltd. specializes in high-performance insole production, offering tailored solutions for brands across the globe. Whether you're launching a new insole collection or expanding your existing product line, we provide OEM/ODM services built around your unique design and performance goals.

From small-batch custom orders to full-scale mass production, our flexible insole manufacturing capabilities adapt to your business needs. With expertise in PU, latex, and graphene insole materials, we turn ideas into functional, comfortable, and market-ready insoles that deliver value.

Contact us today to discuss your next insole project. Let GuangXin help you create custom insoles that stand out, perform better, and reflect your brand’s commitment to comfort, quality, and sustainability.

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Latex pillow OEM production facility in Taiwan

Are you looking for a trusted and experienced manufacturing partner that can bring your comfort-focused product ideas to life? GuangXin Industrial Co., Ltd. is your ideal OEM/ODM supplier, specializing in insole production, pillow manufacturing, and advanced graphene product design.

With decades of experience in insole OEM/ODM, we provide full-service manufacturing—from PU and latex to cutting-edge graphene-infused insoles—customized to meet your performance, support, and breathability requirements. Our production process is vertically integrated, covering everything from material sourcing and foaming to molding, cutting, and strict quality control.Eco-friendly pillow OEM manufacturer Thailand

Beyond insoles, GuangXin also offers pillow OEM/ODM services with a focus on ergonomic comfort and functional innovation. Whether you need memory foam, latex, or smart material integration for neck and sleep support, we deliver tailor-made solutions that reflect your brand’s values.

We are especially proud to lead the way in ESG-driven insole development. Through the use of recycled materials—such as repurposed LCD glass—and low-carbon production processes, we help our partners meet sustainability goals without compromising product quality. Our ESG insole solutions are designed not only for comfort but also for compliance with global environmental standards.Vietnam athletic insole OEM supplier

At GuangXin, we don’t just manufacture products—we create long-term value for your brand. Whether you're developing your first product line or scaling up globally, our flexible production capabilities and collaborative approach will help you go further, faster.China graphene material ODM solution

📩 Contact us today to learn how our insole OEM, pillow ODM, and graphene product design services can elevate your product offering—while aligning with the sustainability expectations of modern consumers.Pillow ODM design company in Thailand

Neuron densities in cortical areas in the mammalian brain follow a consistent distribution pattern. This finding that has profound implications for brain modeling and the development of brain-inspired technologies. Credit: Morales-Gregorio Human Brain Project researchers from Forschungszentrum Jülich and the University of Cologne (Germany) have uncovered how neuron densities are distributed across and within cortical areas in the mammalian brain. They have unveiled a fundamental organizational principle of cortical cytoarchitecture: the ubiquitous lognormal distribution of neuron densities. Numbers of neurons and their spatial arrangement play a crucial role in shaping the brain’s structure and function. Yet, despite the wealth of available cytoarchitectonic data, the statistical distributions of neuron densities remain largely undescribed. The new Human Brain Project (HBP) study, published in the journal Cerebral Cortex, advances our understanding of the organization of mammalian brains. Analyzing the Datasets and the Lognormal Distribution Nine publicly available datasets of seven species (mouse, marmoset, macaque, galago, owl monkey, baboon, and human) provided the foundation for the research team’s investigations. After analyzing the cortical areas of each, they found that neuron densities within these areas follow a consistent pattern – a lognormal distribution. This suggests a fundamental organizational principle underlying the densities of neurons in the mammalian brain. A lognormal distribution is a statistical distribution characterized by a skewed bell-shaped curve. It arises, for instance, when taking the exponential of a normally distributed variable. It differs from a normal distribution in several ways. Most importantly, the curve of a normal distribution is symmetric, while the lognormal one is asymmetric with a heavy tail. Implications and Relevance of Findings These insights are pivotal for precise brain modeling. “Not least because the distribution of neuron densities influences the network connectivity,” says Sacha van Albada, leader of the Theoretical Neuroanatomy group at Forschungszentrum Jülich and senior author of the paper. “For instance, if the density of synapses is constant, regions with lower neuron density will receive more synapses per neuron,” she explains. Such aspects are also relevant for the design of brain-inspired technology such as neuromorphic hardware. “Furthermore, as cortical areas are often distinguished on the basis of cytoarchitecture, knowing the distribution of neuron densities can be relevant for statistically assessing differences between areas and the locations of the borders between areas,” van Albada adds. Understanding the Lognormal Distribution in Brain Characteristics The results align with previous observations that surprisingly many characteristics of the brain follow a lognormal distribution. “One reason why it may be very common in nature is because it emerges when taking the product of many independent variables,” says Alexander van Meegen, joint first author of the study. In other words, the lognormal distribution arises naturally as a result of multiplicative processes, similar to how the normal distribution emerges when many independent variables are summed. “Using a simple model, we were able to show how the multiplicative proliferation of neurons during development may lead to the observed neuron density distributions” explains van Meegen. According to the study, in principle, cortex-wide organizational structures might be by-products of development or evolution that serve no computational function; but the fact that the same organizational structures can be observed for several species and across most cortical areas suggests that the lognormal distribution serves some purpose. “We cannot be sure how the lognormal distribution of neuron densities will influence brain function, but it will likely be associated with high network heterogeneity, which may be computationally beneficial,” says Aitor Morales-Gregorio, first author of the study, citing previous works that suggest that heterogeneity in the brain’s connectivity may promote efficient information transmission. In addition, heterogeneous networks support robust learning and enhance the memory capacity of neural circuits. Reference: “Ubiquitous lognormal distribution of neuron densities in mammalian cerebral cortex” by Aitor Morales-Gregorio, Alexander van Meegen and Sacha J van Albada, 6 July 2023, Cerebral Cortex. DOI: 10.1093/cercor/bhad160

Artist rendering of early Earth. Credit: NASA A new study is taking the air out of a hypothesis linking early Earth’s oxygenation to larger, more complex organisms. Georgia Tech researchers report a more complex effect. Scientists have long thought that there was a direct connection between the rise in atmospheric oxygen, which started with the Great Oxygenation Event 2.5 billion years ago, and the rise of large, complex multicellular organisms. That theory, the “Oxygen Control Hypothesis,” suggests that the size of these early multicellular organisms was limited by the depth to which oxygen could diffuse into their bodies. The hypothesis makes a simple prediction that has been highly influential within both evolutionary biology and geosciences: Greater atmospheric oxygen should always increase the size to which multicellular organisms can grow. It’s a hypothesis that’s proven difficult to test in a lab. Yet a team of Georgia Tech researchers found a way — using directed evolution, synthetic biology, and mathematical modeling — all brought to bear on a simple multicellular lifeform called a ‘snowflake yeast’. The results? Significant new information on the correlations between oxygenation of the early Earth and the rise of large multicellular organisms — and it’s all about exactly how much O2 was available to some of our earliest multicellular ancestors. “The positive effect of oxygen on the evolution of multicellularity is entirely dose-dependent — our planet’s first oxygenation would have strongly constrained, not promoted, the evolution of multicellular life,” explains G. Ozan Bozdag, research scientist in the School of Biological Sciences and the study’s lead author. “The positive effect of oxygen on multicellular size may only be realized when it reaches high levels.” “Oxygen suppression of macroscopic multicellularity” was recently published in the journal Nature Communications. Bozdag’s co-authors on the paper include Georgia Tech researchers Will Ratcliff, associate professor in the School of Biological Sciences; Chris Reinhard, associate professor in the School of Earth and Atmospheric Sciences; Rozenn Pineau, Ph.D. student in the School of Biological Sciences and the Interdisciplinary Graduate Program in Quantitative Biosciences (QBioS); along with Eric Libby, assistant professor at Umea University in Sweden and the Santa Fe Institute in New Mexico. Directing yeast to evolve in record time “We show that the effect of oxygen is more complex than previously imagined. The early rise in global oxygen should in fact strongly constrain the evolution of macroscopic multicellularity, rather than selecting for larger and more complex organisms,” notes Ratcliff. “People have long believed that the oxygenation of Earth’s surface was helpful — some going so far as to say it is a precondition — for the evolution of large, complex multicellular organisms,” he adds. “But nobody has ever tested this directly, because we haven’t had a model system that is both able to undergo lots of generations of evolution quickly, and able to grow over the full range of oxygen conditions,” from anaerobic conditions up to modern levels. The researchers were able to do that, however, with snowflake yeast, simple multicellular organisms capable of rapid evolutionary change. By varying their growth environment, they evolved snowflake yeast for over 800 generations in the lab with selection for larger size. The results surprised Bozdag. “I was astonished to see that multicellular yeast doubled their size very rapidly when they could not use oxygen, while populations that evolved in the moderately oxygenated environment showed no size increase at all,” he says. “This effect is robust — even over much longer timescales.” Size — and oxygen levels — matter for multicellular growth In the team’s research, “large size easily evolved either when our yeast had no oxygen or plenty of it, but not when oxygen was present at low levels,” Ratcliff says. “We did a lot more work to show that this is actually a totally predictable and understandable outcome of the fact that oxygen, when limiting, acts as a resource — if cells can access it, they get a big metabolic benefit. When oxygen is scarce, it can’t diffuse very far into organisms, so there is an evolutionary incentive for multicellular organisms to be small — allowing most of their cells access to oxygen — a constraint that is not there when oxygen simply isn’t present, or when there’s enough of it around to diffuse more deeply into tissues.” Ratcliff says not only does his group’s work challenge the Oxygen Control Hypothesis, it also helps scientists understand why so little apparent evolutionary innovation was happening in the world of multicellular organisms in the billion years after the Great Oxygenation Event. Ratcliff explains that geologists call this period the “Boring Billion” in Earth’s history — also known as the Dullest Time in Earth’s History, and Earth’s Middle Ages — a period when oxygen was present in the atmosphere, but at low levels, and multicellular organisms stayed relatively small and simple. Bozdag adds another insight into the unique nature of the study. “Previous work examined the interplay between oxygen and multicellular size mainly through the physical principles of gas diffusion,” he says. “While that reasoning is essential, we also need an inclusive consideration of principles of Darwinian evolution when studying the origin of complex multicellular life on our planet.” Finally being able to advance organisms through many generations of evolution helped the researchers accomplish just that, Bozdag adds. Reference: “Oxygen suppression of macroscopic multicellularity” by G. Ozan Bozdag, Eric Libby, Rozenn Pineau, Christopher T. Reinhard and William C. Ratcliff, 14 May 2021, Nature Communications. DOI: 10.1038/s41467-021-23104-0 This work was supported by National Science Foundation grant no. DEB-1845363 to W.C.R, NSF grant no. IOS-1656549 to W.C.R., NSF grant no. IOS-1656849 to E.L., and a Packard Foundation Fellowship for Science and Engineering to W.C.R. C.T.R. and W.C.R. acknowledge funding from the NASA Astrobiology Institute.

Researchers from the Telomere-to-Telomere (T2T) consortium have successfully sequenced the complex Y chromosome, adding 30 million new bases to the human genome reference. This accomplishment reveals 41 new protein-coding genes and promises to revolutionize studies on reproduction, evolution, and population changes. The Telomere-to-Telomere consortium has fully sequenced the Y chromosome, uncovering 41 new genes and adding 30 million new bases to the human genome. This breakthrough will impact studies on reproduction, evolution, and human population changes, and correct previous misidentifications of bacterial DNA. Future endeavors aim to integrate this data into the human pangenome for global research collaborations. For decades, the Y chromosome – one of the two human sex chromosomes – has been notoriously challenging for the genomics community to sequence due to the complexity of its structure. Now, this elusive area of the genome has been fully sequenced, a feat that finally completes the set of end-to-end human chromosomes and adds 30 million new bases to the human genome reference, mostly from challenging-to-sequence satellite DNA. These bases reveal 41 additional protein-coding genes, and provide crucial insight for those studying important questions related to reproduction, evolution, and population change. Researchers from the Telomere-to-Telomere (T2T) consortium, which is co-led by the University of California, Santa Cruz Assistant Professor of Biomolecular Engineering Karen Miga, announced this achievement in a new paper to be published today (August 23) in the journal Nature. The complete, annotated Y chromosome reference is available for use on the UCSC Genome Browser and can be accessed via Github. “Just a few years ago, half of the human Y chromosome was missing [from the reference] – the challenging, complex satellite areas,” said Monika Cechova, co-lead author on the paper and postdoctoral scholar in biomolecular engineering at UCSC. “Back then we didn’t even know if it could be sequenced, it was so puzzling. This is really a huge shift in what’s possible.” Until recently, about half of the human Y chromosome was missing from the reference genome. Now, scientists have sequenced this chromosome from end to end. Credit: Darryl Leja, National Human Genome Research Institute (NHGRI) Decoding the Y Chromosome When scientists and clinicians study an individual’s genome, they compare the individuals’ DNA to that of a standard reference to determine where there is variation. Until now, the Y chromosome portion of the human genome has contained large gaps which made it difficult to understand variation and associated disease. The structure of the Y chromosome has been challenging to decode because some of the DNA is organized in palindromes – long sequences that are the same forward and backward – spanning up to more than a million base pairs. Moreover, a very large part of the Y chromosome that was missing from the previous version of the Y reference is satellite DNA – large, highly repetitive regions of non-protein-coding DNA. On the Y chromosome, two satellites are interlinked with each other, further complicating the sequencing process. Karen Miga. Credit: Nick Gonzales/UC Santa Cruz The researchers were able to achieve a gapless read of the Y chromosome due to advances in long-read sequencing technology and new, innovative computational assembly methods that could deal with the repetitive sequences and transform the raw data from sequencing into a usable resource. These new method assemblies allowed the team to tackle some of the particularly challenging aspects of the Y chromosome, such as pinpointing precisely where an inversion occurs in a palindromic sequence — a technique that can be used to find other inversions. The methods established in the paper will allow scientists to complete more end-to-end reads of human Y chromosomes to get a better understanding of how this genetic material affects the diverse human population. “It was the Y chromosome that lacked the most sequences from the previous reference genome,” said Arang Rhie, a staff scientist at the National Human Genome Research Institute and the paper’s lead author. “It was always irritating knowing we were missing half the Y whenever we tried to do any reference-based analysis. I was really excited to curate the first complete Y, to see what we were actually missing, and what we can now do.” The Path to Completion In 2018, Miga and her colleagues released the first complete map of a human centromere on the Y chromosome. This first gap closure was credited to access to ultra-long data, which builds on nanopore sequencing technology that has its origins here at UCSC. It was clear at that point that emerging technology and high-coverage long-read datasets had the potential to complete entire chromosomes end to end, which led to the launch of the T2T Consortium, co-led by Phillippy and Miga. Now, just five years later, the T2T consortium has filled in 30 million additional base pairs, in addition to the first fully sequenced human genome (all the autosomes and the X chromosome) that was released in 2022. Karen Miga in the lab. Credit: Carolyn Lagattuta / UC Santa Cruz Enabling New Research and Discoveries The Y chromosome is most commonly associated with male individuals, but may be found in others, such as intersex people. The sex characteristics regulated by DNA on the Y chromosome are also not equivalent to an individual’s gender identity. While there are relatively few genes on the Y chromosome, the ones that are present are complex and dynamic, and code for important functions such as spermatogenesis, the production of sperm. The complete Y chromosome reference will allow scientists to better study a myriad of features about this part of the human genome in a way that has never before been possible. The complex structure of the Y chromosome has lent itself to rapid evolution within its gene families. In fact, the Y chromosome is the most rapidly changing human chromosome, and even the most rapidly changing chromosome among great apes. This means two healthy people’s Y chromosomes can look very different – for example, one person might have 40 copies of one gene, while another person has 19 copies. This evolution can now be better studied using the new reference and the established methods for sequencing Y chromosomes. This could be the future focus of in vitro fertilization clinics or other research on reproduction and infertility. The end-to-end Y chromosome sequence is a hugely important resource for those studying human population evolution and drift. This is because the Y chromosome is inherited from generation to generation in one group of genetic material, with very little recombination outside of that group, unlike the autosomes and genes on the human X chromosome which often recombine and share genetic material with each other. Having a clearer picture of the Y chromosome makes it easier to track genes across generations of inheritance and learn how the location and content of genes has changed over time. The 30 million new bases added to the Y chromosome reference will also be crucial for studying genome evolution. It will now be possible to study specific and unique Y chromosome sequence patterns, such as the structure of the two satellites and the location and copy numbers of the genes. Even within the Y chromosome, the genes are split into several regions, which are very different from each other in terms of content, structure, and evolutionary history. Understanding rates of change on the Y chromosome and how to interpret this change are intriguing questions that will now be possible to study using the techniques developed in this paper to completely sequence human Y chromosomes. The richer reference that includes the full sequence of the Y chromosome satellite DNA will also allow scientists to better understand the evolutionary relationship of these sequences with satellite DNA found elsewhere on the genome. “It is exciting to be able to finally see these sequences in heterochromatic [densely-packed] regions for the first time. Finally, we can design experiments to test the impact and function of these previously unexplored parts of the Y chromosome,” Miga said. It’s been shown that people with Y chromosomes can lose some or all of that genetic material as they age, but scientists have never fully understood why this happens and the effects it may have. The complete Y chromosome reference may help to illuminate this mystery. It will also be easier to study conditions and disorders that are linked to the Y chromosome, such as the lack of sperm production which leads to infertility. Contamination in Bacterial Genomes An unexpected finding from this paper was that Y chromosome DNA has been repeatedly mistaken to be bacterial DNA in past studies due to the incomplete removal of human contamination in bacterial DNA. This discovery promises to improve the study of bacterial species’ genomes. Human DNA can appear as a contaminant in the genomic samples of bacterial species because the bacterial DNA is often taken from swipes off of human skin. Scientists use the current human genome reference to identify which sequences come from human contamination and remove those, leaving just the bacterial DNA for their study. But, because large parts of the human Y chromosome were missing from the past human reference, scientists were not able to identify them as human and thus mistook them to be part of the DNA of the species they were studying. This paper finds evidence that about 5,000 bacterial genomes in a common database likely contained contamination matching human Y sequences. The groups studying these bacterial species can use the updated Y reference to correctly remove all human contamination from their reference genomes and get a clearer understanding of the bacterial genome. “That was a surprising thing,” Rhie said. “People were guessing at it, but no one could prove that this was happening until now.” Pangenome Y and Future Directions While the complete human Y chromosome will open the door to many new discoveries, the researchers plan to further improve the study of this region by including the Y chromosome in future versions of the human pangenome. The pangenome is a new reference for genomics that combines the genomic information of multiple people from various ancestral backgrounds to ultimately enable more equitable research and clinical discoveries such as helping to diagnose disease, predict medical outcomes, and guide treatments. In collaboration with the Human Pangenome Reference Consortium, the researchers plan to incorporate complete Y chromosome sequences into the individual genomes that make up the pangenome. This will help scientists understand how the Y chromosome varies among people of different ancestral backgrounds and provide a better point of reference for understanding the Y across the diversity of the human population. The researchers hope to be able to collaborate with scientists around the world to enable others to complete Y chromosome sequencing. “We aim to make these data widely accessible,” Miga said. “By creating and sharing these important catalogs of genetic differences on the Y chromosome, we can expand genetic studies of human disease and provide new insights into basic biology.” For more on this breakthrough, see Complete Human Y Chromosome Sequence Assembled for the First Time. Reference: “The complete sequence of a human Y chromosome” by Arang Rhie, Sergey Nurk, Monika Cechova, Savannah J. Hoyt, Dylan J. Taylor, Nicolas Altemose, Paul W. Hook, Sergey Koren, Mikko Rautiainen, Ivan A. Alexandrov, Jamie Allen, Mobin Asri, Andrey V. Bzikadze, Nae-Chyun Chen, Chen-Shan Chin, Mark Diekhans, Paul Flicek, Giulio Formenti, Arkarachai Fungtammasan, Carlos Garcia Giron, Erik Garrison, Ariel Gershman, Jennifer L. Gerton, Patrick G. S. Grady, Andrea Guarracino, Leanne Haggerty, Reza Halabian, Nancy F. Hansen, Robert Harris, Gabrielle A. Hartley, William T. Harvey, Marina Haukness, Jakob Heinz, Thibaut Hourlier, Robert M. Hubley, Sarah E. Hunt, Stephen Hwang, Miten Jain, Rupesh K. Kesharwani, Alexandra P. Lewis, Heng Li, Glennis A. Logsdon, Julian K. Lucas, Wojciech Makalowski, Christopher Markovic, Fergal J. Martin, Ann M. Mc Cartney, Rajiv C. McCoy, Jennifer McDaniel, Brandy M. McNulty, Paul Medvedev, Alla Mikheenko, Katherine M. Munson, Terence D. Murphy, Hugh E. Olsen, Nathan D. Olson, Luis F. Paulin, David Porubsky, Tamara Potapova, Fedor Ryabov, Steven L. Salzberg, Michael E. G. Sauria, Fritz J. Sedlazeck, Kishwar Shafin, Valery A. Shepelev, Alaina Shumate, Jessica M. Storer, Likhitha Surapaneni, Angela M. Taravella Oill, Françoise Thibaud-Nissen, Winston Timp, Marta Tomaszkiewicz, Mitchell R. Vollger, Brian P. Walenz, Allison C. Watwood, Matthias H. Weissensteiner, Aaron M. Wenger, Melissa A. Wilson, Samantha Zarate, Yiming Zhu, Justin M. Zook, Evan E. Eichler, Rachel J. O’Neill, Michael C. Schatz, Karen H. Miga, Kateryna D. Makova and Adam M. Phillippy, 23 August 2023, Nature. DOI: 10.1038/s41586-023-06457-y

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