High-plex whole slide imaging is quickly becoming an essential tool for studying immune response and understanding biological networks. Yet, key to the workflow is choosing the right analysis approaches to leverage large data sets. Scientists at the University Hospital Erlangen got the chance to learn how to acquire such data using Imaging Mass Cytometry™, and then how to connect the right analysis pipelines combining HistoCat phenotyping methods with a downstream analysis in R. Thank you to the Universitätsklinikum Erlangen for hosting, and to Clara Reichardt, PhD student, and Melissa Klug, Field Application Scientist at Standard BioTools, for sharing their learnings and insights. Interested in hosting a seminar at your institution, or need support in your imaging project? Let us know! https://lnkd.in/g3mBv-UA
Standard BioTools’ Post
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In the EM-object paper, we seamlessly merged publicly available spatial transcriptomics data (10x Visium) with its corresponding H&E image, unlocking new insights from existing data! Ever wondered what insights could be extracted by integrating multiple data layers from your projects? This could provide a deeper understanding of what's going on in the tissue samples and impact drug discovery. Reach out if you want to discuss how to integrate multiomic data! https://lnkd.in/g4JdaFS8 #spatialtranscriptomics #multiomics #spatialbiology Enable Medicine
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I’m pleased to announce that my newest scientific article published on Expert Systems with Applications during my Ph.D. in Informatics Engineering is already available online. This article addresses primary challenges that endure in the drug discovery field, including the multi-domain representation space of Drug-Target Interactions (DTIs), DTI understanding and model explainability, and the modeling of the pharmacological space based on information concerning binding pockets. This work presents a novel end-to-end binding-region-guided Transformer-based architecture that simultaneously predicts the 1D binding pocket and the binding affinity of DTI pairs, where the prediction of the 1D binding pocket guides and conditions the prediction of Drug-Target Affinity (DTA). Furthermore, it is capable of providing increasing DTI and prediction understanding due to the nature of the attention blocks and prediction of the 1D binding pocket. This work is the result of the effort performed by a scientific group composed of me and the following excellent researchers: Professor Joel P. Arrais and Professor José Luis Oliveira. https://lnkd.in/dTsra5kX
TAG-DTA: Binding-region-guided strategy to predict drug-target affinity using transformers
sciencedirect.com
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We’re thrilled to announce that our latest web tool Stain-iT™, developed in partnership with the Biosciences Division (BID) of Thermo Fisher Scientific has been awarded CiteAb’s Digital Science Tool of the Year 2024. Stain-iT enables researchers to plan and optimize their cell staining experiments. By selecting the preferred sample fixation status and choosing specific cellular structures to stain, researchers can preview how different dyes and probes will interact with their samples, helping ensuring their purchased products deliver optimal results in the lab. Launched as an MVP last April, its intuitive features and user-friendly interface have led to a growing fan-base amongst researchers worldwide. With more updates planned for later this year, the best of Stain-iT™ is yet to come! With this award-winning tool and our ongoing commitment to innovation, we continue to design and develop revolutionary digital science solutions to help empower scientists worldwide. For Research Use Only. Not for use in diagnostic procedures. #AwardWinning #Innovation https://lnkd.in/e_pv7zxG
Digital Science Tool of the Year - CiteAb Awards 2024
citeab.com
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"BioPhysical and Active Learning Screening (BioPALS), a rapid and versatile hit identification protocol combining AI-powered virtual screening with a confirmation workflow based on GCI and a suite of other orthogonal in vitro biophysical methods"...
Full professor of Medicinal Chemistry & Chemical Biology at the University of Salerno; Secretary of the EFMC Executive Committee; Chair of the Editorial Board of ChemMedChem
A new paper by Concept Life Sciences, just accepted as ChemMedChem (Chemistry Europe) Early View Article, reports the development of BioPhysical and Active Learning Screening (BioPALS), a rapid and versatile hit identification protocol combining AI-powered virtual screening with a confirmation workflow based on GCI and a suite of other orthogonal in vitro biophysical methods. Its application to the BRPF1b bromodomain afforded a range of novel micromolar binders with favorable ADMET properties, showing the versatility and robustness of BioPALS. Accelerating BRPF1b hit identification with BioPhysical and Active Learning Screening (BioPALS) Sandeep Pal, Zandile Nare, Vincenzo A. Rao, Brian O. Smith, Ian Morrison, Edward A. Fitzgerald, Andrew Scott, Tilly (Matilda) Bingham, Thomas Pesnot (FRSC) https://lnkd.in/dBEBU6sv
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#Podcast now available! Experts recently took part in a Podcast to discuss application of multiomics to novel target discovery in #immunooncology Eran Ophir (Chief Scientific Officer, Compugen) and Yaron Turpaz ירון טורפז (Senior Vice President and Senior Advisor, Data and Informatics Solutions, Compugen) discuss the advantages of using multi-omic and #computational approaches for the discovery of novel targets and mechanisms of action of novel drug candidates in immuno-oncology. Listen to the #podcast or read the transcript here to grow your knowledge, as we address questions including: · How are they applying multiomics to novel target discovery in the I–O space? · What advantages do multiomics approaches offer? What is the cutting edge currently in this space? · What is Compugen’s computational approach to developing its I–O pipeline? · The development of diagnostic and prognostic biomarkers remains a key challenge for the I–O space. How can computational approaches help in these efforts? Listen to the podcast or read the transcript here:
Applying multiomics to novel target discovery in immuno-oncology
insights.bio
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Continuous investment in technology talents is the way KFBIO promotes the development of digital pathology #KFBIO#Digitalpathology https://lnkd.in/gsxPERu6
KFBIO Successfully Organized a Postdoctoral Report Review Meeting in C...
kfbiopathology.com
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Executive and Thought Leadership in "Gen AI", "Machine Learning", "Artificial Intelligence", "Data Science", "Cloud", "Data Analytics" "MLOps", "AIOps"
#Technology #DataAnalytics #DataDriven Beyond AlphaFold: The Future Of LLM in Medicine: AlphaFold leaves a complex legacy: What will be the future of LLM in biology and medicine? Continue reading on Towards Data Science » #MachineLearning #ArtificialIntelligence #DataScience
Beyond AlphaFold: The Future Of LLM in Medicine
towardsdatascience.com
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Great course, with hands on practical and data-analytical workshops, as well as inspirational talks by invited scientists.
We are hosting a DDEA PhD course on Quantitative 3D imaging at RUC in January. Bioimaging is being used increasingly in life-science research and instrumentation is available at most universities and through national infrastructures. Even though these technologies are at your fingertips, how do you know which instrument to choose? How to generate high quality quantitative data? What methods should you choose for analysing the data? This course helps answer those questions and gives you the confidence and inspiration to apply bioimaging to answer your specific research questions. Sign up here: https://lnkd.in/ejWPRDM5 #ddeacademy #danishbioimaging #bioimaging
Quantitative 3D Bioimaging PhD Course
https://ddeacademy.dk
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Assistant Professor, PhD. Leading the group of Computational Biomedicine at the University of Innsbruck, Austria
🥁 New preprint alert: #Benchmarking second-generation methods for cell-type #deconvolution of #transcriptomic data 👉 https://lnkd.in/diYZPWFW Second-generation #deconvolution methods can be trained with scRNA-seq data to estimate the cellular composition of bulk RNA-seq samples. This flexibility can unlock the deconvolution of any cell type, tissue, and organism, but poses major challenges to methods benchmarking. We put together a unique set of real and simulated datasets to comprehensively benchmark second-generation deconvolution tools in various scenarios, and systematically assess how deconvolution performance is affected by different sources of variation and bias. In addition, we provide the scientific community with an ecosystem of tools and resources, #omnideconv, that strongly simplifies the application, benchmarking, and optimization of deconvolution methods. 👉 omnideconv.org Great collaboration with Markus List ✨ 👏 Kudos to Alexander Dietrich and Lorenzo Merotto for leading this effort, and to all the co-authors: Konstantin P. Bernhard Eder Constantin Zackl Katharina Reinisch Edenhofer Frank Federico Marini Gregor Sturm 🙏 Many thanks to Universität Innsbruck #DiSC Austrian Science Fund FWF Oesterreichische Nationalbank Bundesministerium für Bildung und Forschung #MyeInfoBank for supporting our work We hope our study and set of tools and resources can be helpful to the scientific community 💫
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