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      Machine learning of serum metabolic patterns encodes early-stage lung adenocarcinoma

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          Abstract

          Early cancer detection greatly increases the chances for successful treatment, but available diagnostics for some tumours, including lung adenocarcinoma (LA), are limited. An ideal early-stage diagnosis of LA for large-scale clinical use must address quick detection, low invasiveness, and high performance. Here, we conduct machine learning of serum metabolic patterns to detect early-stage LA. We extract direct metabolic patterns by the optimized ferric particle-assisted laser desorption/ionization mass spectrometry within 1 s using only 50 nL of serum. We define a metabolic range of 100–400 Da with 143 m/z features. We diagnose early-stage LA with sensitivity~70–90% and specificity~90–93% through the sparse regression machine learning of patterns. We identify a biomarker panel of seven metabolites and relevant pathways to distinguish early-stage LA from controls ( p < 0.05). Our approach advances the design of metabolic analysis for early cancer detection and holds promise as an efficient test for low-cost rollout to clinics.

          Abstract

          Early diagnosis significantly improves the probability of successful cancer therapy. Here, the authors develop a technique to analyse serum metabolites and define a biomarker panel for early-stage lung adenocarcinoma diagnosis.

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          Most cited references54

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          Innate Immune Landscape in Early Lung Adenocarcinoma by Paired Single-Cell Analyses

          To guide the design of immunotherapy strategies for patients with early stage lung tumors, we developed a multiscale immune profiling strategy to map the immune landscape of early lung adenocarcinoma lesions to search for tumor-driven immune changes. Utilizing a barcoding method that allows a simultaneous single cell analysis of the tumor, non-involved lung and blood cells together with multiplex tissue imaging to assess spatial cell distribution, we provide a detailed immune cell atlas of early lung tumors. We show that stage I lung adenocarcinoma lesions already harbor significantly altered T cell and NK cell compartments. Moreover, we identified changes in tumor infiltrating myeloid cell (TIM) subsets that likely compromise anti-tumor T cell immunity. Paired single cell analyses thus offer valuable knowledge of tumor-driven immune changes, providing a powerful tool for the rational design of immune therapies. Comparing single tumor cells with adjacent normal tissue and blood from patients with lung adenocarcinoma charts early changes in tumor immunity and provides insights to guide immunotherapy design.
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            Efficient, approximate and parallel Hartree–Fock and hybrid DFT calculations. A ‘chain-of-spheres’ algorithm for the Hartree–Fock exchange

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              Deep learning for cellular image analysis

              Recent advances in computer vision and machine learning underpin a collection of algorithms with an impressive ability to decipher the content of images. These deep learning algorithms are being applied to biological images and are transforming the analysis and interpretation of imaging data. These advances are positioned to render difficult analyses routine and to enable researchers to carry out new, previously impossible experiments. Here we review the intersection between deep learning and cellular image analysis and provide an overview of both the mathematical mechanics and the programming frameworks of deep learning that are pertinent to life scientists. We survey the field's progress in four key applications: image classification, image segmentation, object tracking, and augmented microscopy. Last, we relay our labs' experience with three key aspects of implementing deep learning in the laboratory: annotating training data, selecting and training a range of neural network architectures, and deploying solutions. We also highlight existing datasets and implementations for each surveyed application.
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                Author and article information

                Contributors
                k.qian@sjtu.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                16 July 2020
                16 July 2020
                2020
                : 11
                : 3556
                Affiliations
                [1 ]ISNI 0000 0004 0368 8293, GRID grid.16821.3c, State Key Laboratory for Oncogenes and Related Genes, School of Biomedical Engineering, , Shanghai Jiao Tong University, ; 200030 Shanghai, P. R. China
                [2 ]ISNI 0000 0004 0368 8293, GRID grid.16821.3c, Department of Laboratory Medicine, Shanghai Chest Hospital, , Shanghai Jiao Tong University, ; 200030 Shanghai, P. R. China
                [3 ]iMS Clinic, 310052 Hangzhou, P. R. China
                [4 ]ISNI 0000 0004 1936 7929, GRID grid.263864.d, Department of Chemistry, , Southern Methodist University, ; 3215 Daniel Avenue, Dallas, TX 75275-0314 USA
                Author information
                http://orcid.org/0000-0002-1787-5298
                http://orcid.org/0000-0003-1839-6739
                http://orcid.org/0000-0001-7860-5577
                http://orcid.org/0000-0002-9530-196X
                http://orcid.org/0000-0001-8241-9769
                http://orcid.org/0000-0001-8191-3255
                http://orcid.org/0000-0003-1666-1965
                Article
                17347
                10.1038/s41467-020-17347-6
                7366718
                32678093
                aef10347-dc49-43e4-ba84-44bcac0db4d7
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 22 January 2020
                : 24 June 2020
                Funding
                Funded by: Innovation Group Project of Shanghai Municipal Health Comission (2019CXJQ03) Clinical Research Plan of SHDC (Project 16CR2011A)
                Funded by: FundRef https://doi.org/10.13039/501100001809, National Natural Science Foundation of China (National Science Foundation of China);
                Award ID: 81971771
                Award ID: 81771983
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/501100002855, Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology);
                Award ID: 2017YFE0124400
                Award ID: 2017YFC0909000
                Award Recipient :
                Funded by: Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology)
                Funded by: Shanghai Rising-Star Program (19QA1404800) Shanghai Institutions of Higher Learning (Program for Professor of Special Appointment (Eastern Scholar))
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                mass spectrometry,cancer metabolism,tumour biomarkers,biomedical engineering
                Uncategorized
                mass spectrometry, cancer metabolism, tumour biomarkers, biomedical engineering

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