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      Artificial Intelligence-Aided Massively Parallel Spectroscopy of Freely Diffusing Nanoscale Entities

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          Abstract

          Massively parallel spectroscopy (MPS) of many single nanoparticles in an aqueous dispersion is reported. As a model system, bioconjugated photon-upconversion nanoparticles (UCNPs) with a near-infrared excitation are prepared. The UCNPs are doped either with Tm 3+ (emission 450 and 802 nm) or Er 3+ (emission 554 and 660 nm). These UCNPs are conjugated to biotinylated bovine serum albumin (Tm 3+-doped) or streptavidin (Er 3+-doped). MPS is correlated with an ensemble spectra measurement, and the limit of detection (1.6 fmol L –1) and the linearity range (4.8 fmol L –1 to 40 pmol L –1) for bioconjugated UCNPs are estimated. MPS is used for observing the bioaffinity clustering of bioconjugated UCNPs. This observation is correlated with a native electrophoresis and bioaffinity assay on a microtiter plate. A competitive MPS bioaffinity assay for biotin is developed and characterized with a limit of detection of 6.6 nmol L –1. MPS from complex biological matrices (cell cultivation medium) is performed without increasing background. The compatibility with polydimethylsiloxane microfluidics is proven by recording MPS from a 30 μm deep microfluidic channel.

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          Deep learning.

          Deep learning allows computational models that are composed of multiple processing layers to learn representations of data with multiple levels of abstraction. These methods have dramatically improved the state-of-the-art in speech recognition, visual object recognition, object detection and many other domains such as drug discovery and genomics. Deep learning discovers intricate structure in large data sets by using the backpropagation algorithm to indicate how a machine should change its internal parameters that are used to compute the representation in each layer from the representation in the previous layer. Deep convolutional nets have brought about breakthroughs in processing images, video, speech and audio, whereas recurrent nets have shone light on sequential data such as text and speech.
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            U-Net: Convolutional Networks for Biomedical Image Segmentation

            There is large consent that successful training of deep networks requires many thousand annotated training samples. In this paper, we present a network and training strategy that relies on the strong use of data augmentation to use the available annotated samples more efficiently. The architecture consists of a contracting path to capture context and a symmetric expanding path that enables precise localization. We show that such a network can be trained end-to-end from very few images and outperforms the prior best method (a sliding-window convolutional network) on the ISBI challenge for segmentation of neuronal structures in electron microscopic stacks. Using the same network trained on transmitted light microscopy images (phase contrast and DIC) we won the ISBI cell tracking challenge 2015 in these categories by a large margin. Moreover, the network is fast. Segmentation of a 512x512 image takes less than a second on a recent GPU. The full implementation (based on Caffe) and the trained networks are available at http://lmb.informatik.uni-freiburg.de/people/ronneber/u-net . conditionally accepted at MICCAI 2015
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              Upconversion and anti-Stokes processes with f and d ions in solids.

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                Author and article information

                Journal
                Anal Chem
                Anal Chem
                ac
                ancham
                Analytical Chemistry
                American Chemical Society
                0003-2700
                1520-6882
                08 August 2023
                22 August 2023
                : 95
                : 33
                : 12256-12263
                Affiliations
                [1]Institute of Analytical Chemistry of the Czech Academy of Sciences , Veveří 97, 602 00 Brno, Czech Republic
                Author notes
                Author information
                https://orcid.org/0000-0003-3358-3858
                https://orcid.org/0000-0002-8421-6583
                Article
                10.1021/acs.analchem.3c01043
                10448498
                37552526
                6cd54b81-8310-4a7a-b7a2-6d5990be6d77
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 08 March 2023
                : 25 July 2023
                Funding
                Funded by: Grantová Agentura Ceské Republiky, doi 10.13039/501100001824;
                Award ID: 21-03156S
                Categories
                Article
                Custom metadata
                ac3c01043
                ac3c01043

                Analytical chemistry
                Analytical chemistry

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