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	<title>subcutaneous fat &#8211; Science</title>
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	<title>subcutaneous fat &#8211; Science</title>
	<link>https://scienmag.com</link>
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		<title>CT body-composition changes precede pancreatic cancer diagnosis</title>
		<link>https://scienmag.com/ct-body-composition-changes-precede-pancreatic-cancer-diagnosis/</link>
		
		<dc:creator><![CDATA[Nathaniel Bowman]]></dc:creator>
		<pubDate>Tue, 20 Oct 2026 20:17:24 +0000</pubDate>
				<category><![CDATA[Cancer]]></category>
		<category><![CDATA[Artificial Intelligence]]></category>
		<category><![CDATA[artificial intelligence in medical imaging]]></category>
		<category><![CDATA[body]]></category>
		<category><![CDATA[body composition]]></category>
		<category><![CDATA[composition]]></category>
		<category><![CDATA[CT body composition analysis]]></category>
		<category><![CDATA[CT scans]]></category>
		<category><![CDATA[early biomarkers for pancreatic cancer]]></category>
		<category><![CDATA[early detection]]></category>
		<category><![CDATA[longitudinal CT scan analysis for cancer prediction]]></category>
		<category><![CDATA[Mayo Clinic]]></category>
		<category><![CDATA[non-invasive imaging for pancreatic cancer screening]]></category>
		<category><![CDATA[pancreatic cancer]]></category>
		<category><![CDATA[pancreatic cancer early detection]]></category>
		<category><![CDATA[pancreatic ductal adenocarcinoma]]></category>
		<category><![CDATA[prediagnostic body composition markers]]></category>
		<category><![CDATA[predictive value of CT scans in pancreatic cancer diagnosis]]></category>
		<category><![CDATA[role of body fat and muscle changes in cancer detection]]></category>
		<category><![CDATA[skeletal muscle]]></category>
		<category><![CDATA[skeletal muscle changes prior to pancreatic cancer diagnosis]]></category>
		<category><![CDATA[subcutaneous fat]]></category>
		<category><![CDATA[subcutaneous fat loss in pancreatic ductal adenocarcinoma]]></category>
		<category><![CDATA[visceral fat]]></category>
		<category><![CDATA[visceral fat decline before pancreatic cancer]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=322287</guid>

					<description><![CDATA[A Mayo Clinic cohort study found that steeper fat loss and emerging muscle differences on CT scans were associated with pancreatic ductal adenocarcinoma during the years before diagnosis.]]></description>
										<content:encoded><![CDATA[<p>People who later develop pancreatic ductal adenocarcinoma (PDAC) show steeper declines in visceral and subcutaneous fat than matched patients without pancreatic cancer during the three years before diagnosis, according to a peer-reviewed Mayo Clinic study published in <i>Pancreatology</i>. The analysis also found that differences in skeletal muscle were most apparent during the final 12 months before diagnosis. Together, the findings indicate that routinely acquired CT scans may capture measurable body-composition changes associated with pancreatic cancer before it is clinically detected.</p>
<p>The researchers analyzed abdominal CT scans from 1,825 patients with PDAC and 3,650 matched controls from Mayo Clinic sites in Arizona, Florida and Minnesota. They used an artificial intelligence-based body-composition tool to measure changes in skeletal muscle, subcutaneous fat and visceral fat over time. By comparing longitudinal measurements between patients who developed pancreatic cancer and similar individuals without cancer, the investigators assessed whether the timing and rate of body-composition changes differed before diagnosis. The study is observational, so it shows an association between prediagnostic changes and subsequent PDAC rather than proving that those changes cause the disease or that CT-based measurements can screen for it.</p>
<p>The strongest observed difference was a significantly steeper decline in both subcutaneous and visceral fat during the three years before PDAC diagnosis among patients who developed the disease. Muscle differences were less apparent over the full period but became most pronounced in the year immediately preceding diagnosis. When the researchers evaluated whether the muscle and fat measurements could distinguish patients who later developed pancreatic cancer from matched controls, the measures demonstrated moderate discriminatory ability. This supports their potential to provide additional information in future risk-assessment strategies, but the study did not establish a complete clinical prediction model, evaluate a prospective screening program or demonstrate improved patient outcomes.</p>
<p>The results may be relevant to efforts to identify pancreatic cancer earlier because PDAC can develop silently and is often diagnosed after it has spread. Current surveillance programs focus primarily on people with inherited genetic risk or strong family histories, while most pancreatic cancers occur outside those high-risk groups. The Mayo Clinic analysis is, to the researchers’ knowledge, the largest controlled study to examine prediagnostic body-composition trajectories in patients who later developed pancreatic cancer and one of the first to assess whether those trajectories can help distinguish future cases from controls. Mayo researchers are now developing algorithms that combine body-composition measurements with other routinely collected clinical factors and imaging biomarkers to identify patients at increased risk.</p>
<p><strong>Subject of Research:</strong> Prediagnostic CT body-composition trajectories associated with pancreatic ductal adenocarcinoma</p>
<p><strong>Article Title:</strong> Body composition changes on CT scans may help identify pancreatic cancer risk</p>
<p><strong>Article References:</strong> Body composition changes on CT scans may help identify pancreatic cancer risk. <a href="https://www.eurekalert.org/news-releases/1148511" rel="noopener noreferrer">Original publication</a> (Bibliographic details unavailable.)</p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> Not provided</p>
<p><strong>Keywords:</strong> pancreatic cancer, pancreatic ductal adenocarcinoma, body composition, CT scans, visceral fat, subcutaneous fat, skeletal muscle, artificial intelligence, early detection, Mayo Clinic, Body, composition</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">322287</post-id>	</item>
		<item>
		<title>AI Maps Facial Tissue Depths in Nearly 2,000 CT Scans to Help Identify the Dead</title>
		<link>https://scienmag.com/ai-maps-facial-tissue-depths-in-nearly-2000-ct-scans-to-help-identify-the-dead/</link>
		
		<dc:creator><![CDATA[Ophelia Keating]]></dc:creator>
		<pubDate>Fri, 02 Oct 2026 23:38:09 +0000</pubDate>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[Aging]]></category>
		<category><![CDATA[AI in forensic anthropology]]></category>
		<category><![CDATA[AI-driven facial recognition]]></category>
		<category><![CDATA[AI-enhanced craniofacial mapping]]></category>
		<category><![CDATA[Artificial Intelligence]]></category>
		<category><![CDATA[bilateral symmetry]]></category>
		<category><![CDATA[biometric identification using soft tissue depth]]></category>
		<category><![CDATA[computed tomography]]></category>
		<category><![CDATA[craniofacial soft tissue thickness]]></category>
		<category><![CDATA[craniofacial soft tissue thickness database]]></category>
		<category><![CDATA[CT scan analysis for forensic identification]]></category>
		<category><![CDATA[facial reconstruction]]></category>
		<category><![CDATA[facial tissue thickness at craniofacial landmarks]]></category>
		<category><![CDATA[forensic facial reconstruction]]></category>
		<category><![CDATA[forensic identification]]></category>
		<category><![CDATA[forensic identification methods using CT scans]]></category>
		<category><![CDATA[forensic science]]></category>
		<category><![CDATA[Machine learning]]></category>
		<category><![CDATA[medical imaging for forensic science]]></category>
		<category><![CDATA[population-specific database]]></category>
		<category><![CDATA[population-specific facial tissue measurements]]></category>
		<category><![CDATA[sexual dimorphism]]></category>
		<category><![CDATA[soft tissue measurement in forensic reconstruction]]></category>
		<category><![CDATA[subcutaneous fat]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=229611</guid>

					<description><![CDATA[A study of nearly 2,000 CT scans from northwestern India has built a large AI-assisted database of craniofacial soft tissue and fat thickness to improve forensic facial reconstruction.]]></description>
										<content:encoded><![CDATA[<p>When forensic artists reconstruct a face from a bare skull, they depend on one deceptively simple set of numbers: how thick the soft tissue is at dozens of standardized points on the head. Those values, known as craniofacial soft tissue thickness, act as the bridge between skeletal anatomy and a recognizable human face. A new study from India has now built one of the largest population-specific databases of these measurements ever assembled, and it has used artificial intelligence to squeeze far more information out of them than traditional averages allow.</p>
<p>The research, published in the International Journal of Legal Medicine, was led by Sushil Kumar Battan and colleagues at the Postgraduate Institute of Medical Education and Research in Chandigarh together with collaborators at Chandigarh University. The team carried out a retrospective cross-sectional analysis of computed tomography scans from 1,972 individuals aged between 18 and 80 years, all drawn from a northwestern Indian population. Rather than relying on the mean tissue depths that have dominated facial reconstruction practice for decades, the researchers measured both total craniofacial soft tissue thickness and the subcutaneous fat layer thickness separately, at 73 standardized craniofacial landmarks.</p>
<p>The distinction matters because the total thickness at any point on the face is not a single uniform material. It is a composite of skin, muscle, fascia, glands and fat, and only the subcutaneous fat component changes dramatically with age, sex, nutrition and body composition. Most existing reference tables, including large in vivo databases assembled for European populations, collapse all of these layers into a single number. By separating the adipose from the non-adipose contribution, the Indian dataset offers reconstructers a two-parameter description of facial architecture, which in principle allows far more nuanced modeling of how a face would have looked in life.</p>
<p>Technically, the measurements were extracted from CT imaging, which provides the millimeter-scale resolution needed to delineate the boundary between the bone, the deeper soft tissues and the subcutaneous fat plane. The statistical analysis combined classical tools with machine learning. Descriptive statistics established the baseline distributions at each landmark, independent t-tests quantified differences between the sexes, analysis of variance tested variation across age groups, and Pearson correlation assessed how tightly the two thickness measures track each other. On top of this, the team trained regression and machine learning algorithms to predict tissue thicknesses and to evaluate how well different variables explain the observed variation.</p>
<p>The results confirm that total soft tissue thickness consistently exceeds fat layer thickness at every one of the 73 landmarks, underscoring that a substantial portion of facial volume comes from muscle and other non-adipose structures. At the level of individual landmarks, the correlation between the two measures was strong, with a coefficient of determination of roughly 0.785, meaning that about three quarters of the landmark-level variation in total thickness can be accounted for by the fat layer alone. Interestingly, that relationship weakens dramatically when data are aggregated by age group, where the correlation drops to about 0.143. This suggests that while fat is a dominant driver of thickness at any given anatomical point, age-related changes in the two layers follow partially independent trajectories, likely reflecting muscle atrophy and connective tissue remodeling that proceed on different schedules from fat redistribution.</p>
<p>Sexual dimorphism emerged clearly in the data, with males showing higher values than females across the landmark set, although the effect sizes were small. That combination of statistical significance and modest magnitude is a familiar pattern in facial anthropometry and carries a practical warning for forensic practitioners: knowing the sex of a skull helps narrow the expected tissue depths, but it does not remove the need for population- and age-appropriate reference values. The age analysis revealed a classic increase-peak-decline pattern, with thickness measurements rising through early adulthood, reaching a maximum in middle adulthood and then declining in older age groups, mirroring the well-documented trajectory of facial fat compartments and the progressive resorption of the underlying facial skeleton.</p>
<p>One of the most striking findings concerns symmetry. When the researchers compared measurements taken on the right and left sides of the same faces, they found an extremely high correlation, with a coefficient of determination of 0.992. For forensic facial approximation, this is reassuring news, because it means that reference values collected on one side of the head can be applied to the other with negligible loss of accuracy, and that genuine bilateral asymmetry in soft tissue depth is rare enough to be treated as an exception rather than a rule in reconstruction work.</p>
<p>The artificial intelligence component of the study is where the project pushes furthest beyond conventional practice. The team compared machine learning models against standard linear regression and found that the best-performing algorithms, particularly a Random Forest model, achieved coefficients of determination exceeding 0.90 within the dataset, outperforming conventional approaches and showing limited systematic bias. Random Forest methods work by building an ensemble of decision trees, each trained on random subsets of the data and features, and averaging their predictions; this makes them well suited to capturing the nonlinear interactions between age, sex, landmark position and body composition that govern facial tissue thickness, interactions that a single linear equation cannot represent.</p>
<p>The authors are careful to flag the central limitation of these results: the models demonstrated strong within-dataset performance, but independent external validation is required before the predictions can be trusted on new populations or imaging systems. A model that achieves an R-squared above 0.90 on the data it was trained and tested on may still degrade when confronted with scans from a different scanner, a different ancestry group or a different body mass distribution. This caution reflects a broader lesson from the application of machine learning in medical imaging, where promising internal metrics have repeatedly failed to translate without rigorous external testing.</p>
<p>Even with that caveat, the study delivers something the forensic community has long needed: a large, CT-derived, population-specific reference database for a northwestern Indian population, one of the most populous regions of the world that has been underrepresented in facial reconstruction literature. Most established tissue depth tables were built from cadaver measurements or smaller imaging samples of European and East Asian subjects, and applying them to other populations introduces systematic error into reconstructed faces. By integrating total soft tissue thickness and fat layer thickness across 73 landmarks, quantifying sex and age effects, and demonstrating near-perfect bilateral symmetry, the Chandigarh team has produced a foundation for more accurate, data-driven facial approximation. As AI-guided craniofacial reconstruction systems mature, datasets of this kind will be the raw material that determines whether a reconstructed face becomes a recognizable likeness or just an anatomical guess.</p>
<p><strong>Subject of Research:</strong> AI-based CT measurement of craniofacial soft tissue and fat thickness for forensic facial reconstruction in a northwestern Indian population</p>
<p><strong>Article Title:</strong> Artificial intelligence -based modeling and comparative evaluation of craniofacial soft tissue and subcutaneous fat thickness using ct imaging for forensic identification in a northwestern indian population</p>
<p><strong>Article References:</strong> Battan, S. K., Sharma, M., Garg, M., Singh, P., verma, P., &amp; Singla, N. (2026). Artificial intelligence -based modeling and comparative evaluation of craniofacial soft tissue and subcutaneous fat thickness using ct imaging for forensic identification in a northwestern indian population. <em>International Journal of Legal Medicine</em>. <a href="https://doi.org/10.1007/s00414-026-04000-y" rel="noopener noreferrer">https://doi.org/10.1007/s00414-026-04000-y</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1007/s00414-026-04000-y" rel="noopener noreferrer">10.1007/s00414-026-04000-y</a></p>
<p><strong>Keywords:</strong> forensic science, facial reconstruction, craniofacial soft tissue thickness, subcutaneous fat, computed tomography, artificial intelligence, machine learning, sexual dimorphism, aging, bilateral symmetry, forensic identification, population-specific database</p>
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		<post-id xmlns="com-wordpress:feed-additions:1">229611</post-id>	</item>
		<item>
		<title>Scientists Decode Why Tibetan Pig Fat Tastes Better Than Duroc Pork</title>
		<link>https://scienmag.com/scientists-decode-why-tibetan-pig-fat-tastes-better-than-duroc-pork/</link>
		
		<dc:creator><![CDATA[Juliet Wilcox]]></dc:creator>
		<pubDate>Sat, 12 Sep 2026 14:12:54 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[butyric acid]]></category>
		<category><![CDATA[candidate genes]]></category>
		<category><![CDATA[Duroc pigs]]></category>
		<category><![CDATA[fat metabolism]]></category>
		<category><![CDATA[fatty acid metabolites in pigs]]></category>
		<category><![CDATA[fatty acids]]></category>
		<category><![CDATA[gene expression in pig breeds]]></category>
		<category><![CDATA[high-altitude pig adaptation]]></category>
		<category><![CDATA[high-altitude pig genetics]]></category>
		<category><![CDATA[indigenous pig breed meat characteristics]]></category>
		<category><![CDATA[lipid compounds in pork quality]]></category>
		<category><![CDATA[lipidomics]]></category>
		<category><![CDATA[meat flavor science]]></category>
		<category><![CDATA[Meat Quality]]></category>
		<category><![CDATA[molecular basis of pork flavor]]></category>
		<category><![CDATA[multi-omics pork research]]></category>
		<category><![CDATA[pork breeding and flavor improvement]]></category>
		<category><![CDATA[pork flavor]]></category>
		<category><![CDATA[Proteomics]]></category>
		<category><![CDATA[subcutaneous fat]]></category>
		<category><![CDATA[Tibetan pig fat flavor analysis]]></category>
		<category><![CDATA[Tibetan pigs]]></category>
		<category><![CDATA[Tibetan vs Duroc pig fat]]></category>
		<category><![CDATA[transcriptome]]></category>
		<guid isPermaLink="false">https://scienmag.com/?p=195187</guid>

					<description><![CDATA[A multi-omics comparison of Tibetan and Duroc pigs has identified candidate genes and fatty acid biomarkers that may explain why Tibetan pork has a distinctive flavor.]]></description>
										<content:encoded><![CDATA[<p>The secret behind the celebrated flavor of Tibetan pig pork may finally be coming into focus, thanks to an ambitious multi-omics study that has compared the subcutaneous fat of two dramatically different pig breeds at the molecular level. In research published in BMC Genomics, a team of Chinese scientists led by Hao Li, Jie Wu and Yizhi Luo undertook a comprehensive comparison between Tibetan pigs, a hardy breed adapted to the high-altitude environments of the Qinghai-Tibet Plateau, and Duroc pigs, a fast-growing commercial breed widely used in industrial pork production worldwide. By analyzing fatty acid metabolites, proteins and gene expression in subcutaneous fat simultaneously, the researchers assembled one of the most detailed molecular portraits to date of how breed differences translate into meat quality. Their findings point to specific genes, lipid compounds and metabolic pathways that could shape the future of pork breeding and flavor science.</p>
<p>The motivation for the study stems from a growing tension in the global pork industry. Consumers increasingly complain that modern lean-meat breeds sacrifice taste for efficiency, while indigenous breeds such as the Tibetan pig are prized for their distinctive flavor, tender texture and rich aroma. Subcutaneous fat, the layer of fat beneath the skin, is a critical depot in this equation because it stores fatty acids and other compounds that influence juiciness, mouthfeel and the volatile molecules released during cooking. Yet the molecular basis for why Tibetan pig fat tastes different from that of commercial breeds has remained poorly characterized. To close that gap, the research team designed an integrated experiment combining fatty acid metabolomics, quantitative proteomics and transcriptome sequencing on subcutaneous fat samples from both breeds, allowing them to track differences across three layers of biological information.</p>
<p>The scale of the molecular divergence between the two breeds was striking. The analysis revealed 345 differentially abundant lipid compounds between Tibetan and Duroc pigs, alongside 238 differentially expressed proteins and 993 differentially expressed genes in the subcutaneous fat tissue. This tri-layered dataset gave the researchers an unusually complete view of the biological machinery governing fat deposition. Rather than treating each data type in isolation, the team cross-referenced the metabolite, protein and gene profiles to identify molecules whose abundance changes were supported at multiple levels, a strategy that strengthens confidence that the identified factors genuinely influence meat quality rather than being incidental statistical fluctuations.</p>
<p>From this integrated analysis, four candidate genes emerged as particularly important: MT2A, ABHD14B, PDK4 and APOA1. Each of these genes has functions that plausibly connect to fat metabolism and energy handling. PDK4, for example, encodes pyruvate dehydrogenase kinase 4, a well-known regulator of cellular fuel switching that shifts metabolism away from glucose oxidation toward fatty acid utilization. ABHD14B belongs to a family of enzymes involved in lipid hydrolysis and protein modification, while APOA1 encodes apolipoprotein A1, the principal protein component of high-density lipoprotein particles that transport lipids through the bloodstream. MT2A, a metallothionein involved in metal binding and stress responses, adds a further layer of regulatory complexity. The researchers propose that variation in these genes contributes to the differences in subcutaneous fat properties and, by extension, meat quality between Tibetan and Duroc pigs.</p>
<p>Perhaps the most eye-catching single finding concerns butyric acid, a short-chain fatty acid with a strong odor that emerged as a potential biomarker capable of distinguishing Tibetan pigs from Duroc pigs. Short-chain fatty acids like butyric acid are key contributors to the characteristic aromas of aged cheeses and fermented foods, and elevated levels in fat tissue could directly shape the sensory profile of the meat. Alongside butyric acid, the study found higher levels of adenosine triphosphate, or ATP, in Tibetan pig fat. ATP is best known as the universal energy currency of cells, but in meat science it plays a starring role as a precursor of flavor: after slaughter, ATP degrades into inosine monophosphate and other compounds that give cooked meat its savory umami character. Higher ATP reserves may therefore help explain the deeper, more satisfying taste associated with Tibetan pork.</p>
<p>Synthesizing these observations, the researchers propose that the distinctive flavor of Tibetan pigs relative to Durocs may stem from fundamental differences in fat deposition patterns and the efficiency of energy utilization. Tibetan pigs evolved under extreme plateau conditions characterized by cold temperatures, low oxygen and sporadic food availability, pressures that likely shaped a metabolism optimized for storing energy in fat depots rich in flavor-relevant compounds. Duroc pigs, by contrast, have been selectively bred over decades for rapid growth and lean carcasses, an optimization that may come at the expense of the biochemical processes that build flavor. The multi-omics comparison suggests these two evolutionary and agricultural trajectories left measurable fingerprints across the genome, proteome and lipidome of the fat tissue.</p>
<p>The study also raises an intriguing nutritional hypothesis. The subcutaneous fat of Tibetan pigs was found to be rich in triacylglycerols, or TAGs, the molecules that constitute the bulk of dietary fat. The authors suggest that this TAG-rich fat may be more readily absorbed by the human body than the fat of Duroc pigs, a possibility that, if confirmed in controlled digestion and nutrition studies, could reframe how scientists and consumers think about the healthfulness of fat from indigenous breeds. The researchers are careful to note that this absorption question warrants further investigation, and no clinical claims are being made. Nevertheless, the idea that the structure and composition of fat from different breeds could influence digestibility adds a compelling dimension to ongoing debates about fat quality versus fat quantity in human nutrition.</p>
<p>Beyond its immediate scientific findings, the study carries practical implications for livestock breeding. The identification of MT2A, ABHD14B, PDK4 and APOA1 as candidate markers gives breeders potential molecular handles for selecting pigs that combine the growth efficiency of commercial breeds with the flavor attributes of indigenous ones. Marker-assisted selection and genomic editing techniques could, in principle, be directed at these genes or their regulatory networks to engineer pork that satisfies both economic and sensory demands. The metabolite findings, particularly the butyric acid biomarker, could also find application in quality control, offering a chemical signature for authenticating Tibetan pork products in a marketplace where provenance commands a premium.</p>
<p>The research was conducted by teams from the Institute of Animal Science at the Guangdong Academy of Agricultural Sciences, South China Agricultural University and partner institutions, with experimental materials provided by the pig core breeding farms of Wens Foodstuff Group and the Guangdong Academy of Agricultural Sciences. All animal procedures received ethics approval from the Animal Care and Use Committee of the Guangdong Academy of Agricultural Sciences. The work was supported by a suite of Guangdong provincial funding programs focused on seed industry revitalization and rural development, reflecting China&#8217;s broader strategic investment in preserving and exploiting the genetic resources of indigenous livestock breeds. Published as an open-access article, the study offers researchers worldwide a rich dataset for exploring the biology of meat quality.</p>
<p>For now, the molecular story of why a pig raised on the Tibetan Plateau tastes different from one raised in an industrial barn is only beginning to be written. The study establishes a framework linking genes, proteins and lipids to the eating experience, and it delivers a concrete set of candidate markers for the next generation of breeding programs. Whether future work confirms the nutritional advantages of Tibetan pig fat or uncovers additional flavor compounds hiding in its lipidome, the message of this research is clear: the taste of pork is written in the chemistry of fat, and that chemistry can now be read with unprecedented precision. As consumers worldwide demand better-tasting, more authentic food, studies like this one are turning traditional delicacies into guides for the future of animal breeding.</p>
<p><strong>Subject of Research:</strong> Multi-omics analysis of subcutaneous fat in Tibetan and Duroc pigs to identify substances affecting pork meat quality</p>
<p><strong>Article Title:</strong> Identification of important substances in subcutaneous fat affecting meat quality in Tibetan pigs and Duroc by lipid-protein-transcriptome</p>
<p><strong>Article References:</strong> Li, H., Wu, J., Luo, Y., Yao, Z., Ji, Y., Wang, Y., Chen, Y., Li, X., Rao, K., Li, B., Xin, H., Hu, B., Wang, S., Cheng, L., Lin, X., Xu, G., Yang, M., Yang, J., Wu, Z., &#8230; Meng, F. (2026). Identification of important substances in subcutaneous fat affecting meat quality in Tibetan pigs and Duroc by lipid-protein-transcriptome. <em>BMC Genomics</em>. <a href="https://doi.org/10.1186/s12864-026-13331-4" rel="noopener noreferrer">https://doi.org/10.1186/s12864-026-13331-4</a></p>
<p><strong>Image Credits:</strong> AI Generated</p>
<p><strong>DOI:</strong> <a href="https://doi.org/10.1186/s12864-026-13331-4" rel="noopener noreferrer">10.1186/s12864-026-13331-4</a></p>
<p><strong>Keywords:</strong> Tibetan pigs, Duroc pigs, subcutaneous fat, meat quality, fatty acids, lipidomics, proteomics, transcriptome, butyric acid, candidate genes, pork flavor, fat metabolism</p>
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