![]() Garcia Santa Cruz, Beatriz ![]() ![]() in Scientific Reports (2022) The study of complex diseases relies on large amounts of data to build models toward precision medicine. Such data acquisition is feasible in the context of high-throughput screening, in which the quality ... [more ▼] The study of complex diseases relies on large amounts of data to build models toward precision medicine. Such data acquisition is feasible in the context of high-throughput screening, in which the quality of the results relies on the accuracy of the image analysis. Although state-of-the-art solutions for image segmentation employ deep learning approaches, the high cost of manually generating ground truth labels for model training hampers the day-to-day application in experimental laboratories. Alternatively, traditional computer vision-based solutions do not need expensive labels for their implementation. Our work combines both approaches by training a deep learning network using weak training labels automatically generated with conventional computer vision methods. Our network surpasses the conventional segmentation quality by generalising beyond noisy labels, providing a 25% increase of mean intersection over union, and simultaneously reducing the development and inference times. Our solution was embedded into an easy-to-use graphical user interface that allows researchers to assess the predictions and correct potential inaccuracies with minimal human input. To demonstrate the feasibility of training a deep learning solution on a large dataset of noisy labels automatically generated by a conventional pipeline, we compared our solution against the common approach of training a model from a small manually curated dataset by several experts. Our work suggests that humans perform better in context interpretation, such as error assessment, while computers outperform in pixel-by-pixel fne segmentation. Such pipelines are illustrated with a case study on image segmentation for autophagy events. This work aims for better translation of new technologies to real-world settings in microscopy-image analysis. [less ▲] Detailed reference viewed: 213 (18 UL)![]() ; ; et al in Nature metabolism (2022), 4(5), 589-607 Pyruvate dehydrogenase (PDH) is the gatekeeper enzyme of the tricarboxylic acid (TCA) cycle. Here we show that the deglycase DJ-1 (encoded by PARK7, a key familial Parkinson's disease gene) is a pacemaker ... [more ▼] Pyruvate dehydrogenase (PDH) is the gatekeeper enzyme of the tricarboxylic acid (TCA) cycle. Here we show that the deglycase DJ-1 (encoded by PARK7, a key familial Parkinson's disease gene) is a pacemaker regulating PDH activity in CD4(+) regulatory T cells (T(reg) cells). DJ-1 binds to PDHE1-β (PDHB), inhibiting phosphorylation of PDHE1-α (PDHA), thus promoting PDH activity and oxidative phosphorylation (OXPHOS). Park7 (Dj-1) deletion impairs T(reg) survival starting in young mice and reduces T(reg) homeostatic proliferation and cellularity only in aged mice. This leads to increased severity in aged mice during the remission of experimental autoimmune encephalomyelitis (EAE). Dj-1 deletion also compromises differentiation of inducible T(reg) cells especially in aged mice, and the impairment occurs via regulation of PDHB. These findings provide unforeseen insight into the complicated regulatory machinery of the PDH complex. As T(reg) homeostasis is dysregulated in many complex diseases, the DJ-1-PDHB axis represents a potential target to maintain or re-establish T(reg) homeostasis. [less ▲] Detailed reference viewed: 62 (6 UL)![]() Jarazo, Javier ![]() ![]() in Movement Disorders (2021) Detailed reference viewed: 132 (24 UL)![]() Gomez Giro, Gemma ![]() ![]() in Acta Neuropathologica Communications (2020) Detailed reference viewed: 210 (31 UL)![]() Garcia Santa Cruz, Beatriz ![]() ![]() ![]() Poster (2019, November 29) Automation of biological image analysis is essential to boost biomedical research. The study of complex diseases such as neurodegenerative diseases calls for big amounts of data to build models towards ... [more ▼] Automation of biological image analysis is essential to boost biomedical research. The study of complex diseases such as neurodegenerative diseases calls for big amounts of data to build models towards precision medicine. Such data acquisition is feasible in the context of high-throughput screening in which the quality of the results relays on the accuracy of image analysis. Although the state-of-the-art solutions for image segmentation employ deep learning approaches, the high cost of manual data curation is hampering the real use in current biomedical research laboratories. Here, we propose a pipeline that employs deep learning not only to conduct accurate segmentation but also to assist with the creation of high-quality datasets in a less time-consuming solution for the experts. Weakly-labelled datasets are becoming a common alternative as a starting point to develop real-world solutions. Traditional approaches based on classical multimedia signal processing were employed to generate a pipeline specifically optimized for the high-throughput screening images of iPSC fused with rosella biosensor. Such pipeline produced good segmentation results but with several inaccuracies. We employed the weakly-labelled masks produced in this pipeline to train a multiclass semantic segmentation CNN solution based on U-net architecture. Since a strong class imbalance was detected between the classes, we employed a class sensitive cost function: Dice coe!cient. Next, we evaluated the accuracy between the weakly-labelled data and the trained network segmentation using double-blind tests conducted by experts in cell biology with experience in this type of images; as well as traditional metrics to evaluate the quality of the segmentation using manually curated segmentations by cell biology experts. In all the evaluations the prediction of the neural network overcomes the weakly-labelled data quality segmentation. Another big handicap that complicates the use of deep learning solutions in wet lab environments is the lack of user-friendly tools for non-computational experts such as biologists. To complete our solution, we integrated the trained network on a GUI built on MATLAB environment with non-programming requirements for the user. This integration allows conducting semantic segmentation of microscopy images in a few seconds. In addition, thanks to the patch-based approach it can be employed in images with different sizes. Finally, the human-experts can correct the potential inaccuracies of the prediction in a simple interactive way which can be easily stored and employed to re-train the network to improve its accuracy. In conclusion, our solution focuses on two important bottlenecks to translate leading-edge technologies in computer vision to biomedical research: On one hand, the effortless obtention of high-quality datasets with expertise supervision taking advantage of the proven ability of our CNN solution to generalize from weakly-labelled inaccuracies. On the other hand, the ease of use provided by the GUI integration of our solution to both segment images and interact with the predicted output. Overall this approach looks promising for fast adaptability to new scenarios. [less ▲] Detailed reference viewed: 1132 (44 UL)![]() Arias, Jonathan ![]() ![]() ![]() in Scientific Reports (2019) Autophagic processes play a central role in cellular homeostasis. In pathological conditions, the flow of autophagy can be affected at multiple and distinct steps of the pathway. Current analyses tools do ... [more ▼] Autophagic processes play a central role in cellular homeostasis. In pathological conditions, the flow of autophagy can be affected at multiple and distinct steps of the pathway. Current analyses tools do not deliver the required detail for dissecting pathway intermediates. The development of new tools to analyze autophagic processes qualitatively and quantitatively in a more straightforward manner is required. Defining all autophagy pathway intermediates in a high-throughput manner is technologically challenging and has not been addressed yet. Here, we overcome those requirements and limitations by the developed of stable autophagy and mitophagy reporter-iPSC and the establishment of a novel high-throughput phenotyping platform utilizing automated high-content image analysis to assess autophagy and mitophagy pathway intermediates. [less ▲] Detailed reference viewed: 221 (34 UL)![]() Arias, Jonathan ![]() ![]() ![]() in Stem Cell Reports (2017) Detailed reference viewed: 415 (17 UL) |
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