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Marc Aubreville

Publications and source records attributed to Marc Aubreville.

64 records · Page 4Linked to original sources

Fooling the Crowd with Deep Learning-based Methods

Modern, state-of-the-art deep learning approaches yield human like performance in numerous object detection and classification tasks. The foundation for their success is the availability of training datasets of substantially high quantity, which are expensive to create, especially in the field of medical imaging. Recently, crowdsourcing has been applied to create large datasets for a broad range of disciplines. This study aims to explore the challenges and opportunities of crowd-algorithm collaboration for the object detection task of grading cytology whole slide images. We compared the classical crowdsourcing performance of twenty participants with their results from crowd-algorithm collaboration. All participants performed both modes in random order on the same twenty images. Additionally, we introduced artificial systematic flaws into the precomputed annotations to estimate a bias towards accepting precomputed annotations. We gathered 9524 annotations on 800 images from twenty participants organised into four groups in concordance to their level of expertise with cytology. The crowd-algorithm mode improved on average the participants' classification accuracy by 7%, the mean average precision by 8% and the inter-observer Fleiss' kappa score by 20%, and reduced the time spent by 31%. However, two thirds of the artificially modified false labels were not recognised as such by the contributors. This study shows that crowd-algorithm collaboration is a promising new approach to generate large datasets when it is ensured that a carefully designed setup eliminates potential biases.

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Learning New Tricks from Old Dogs -- Inter-Species, Inter-Tissue Domain Adaptation for Mitotic Figure Assessment

For histopathological tumor assessment, the count of mitotic figures per area is an important part of prognostication. Algorithmic approaches - such as for mitotic figure identification - have significantly improved in recent times, potentially allowing for computer-augmented or fully automatic screening systems in the future. This trend is further supported by whole slide scanning microscopes becoming available in many pathology labs and could soon become a standard imaging tool. For an application in broader fields of such algorithms, the availability of mitotic figure data sets of sufficient size for the respective tissue type and species is an important precondition, that is, however, rarely met. While algorithmic performance climbed steadily for e.g. human mammary carcinoma, thanks to several challenges held in the field, for most tumor types, data sets are not available. In this work, we assess domain transfer of mitotic figure recognition using domain adversarial training on four data sets, two from dogs and two from humans. We were able to show that domain adversarial training considerably improves accuracy when applying mitotic figure classification learned from the canine on the human data sets (up to +12.8% in accuracy) and is thus a helpful method to transfer knowledge from existing data sets to new tissue types and species.

cs.CV↗

Deep Learning-Based Quantification of Pulmonary Hemosiderophages in Cytology Slides

Purpose: Exercise-induced pulmonary hemorrhage (EIPH) is a common syndrome in sport horses with negative impact on performance. Cytology of bronchoalveolar lavage fluid by use of a scoring system is considered the most sensitive diagnostic method. Macrophages are classified depending on the degree of cytoplasmic hemosiderin content. The current gold standard is manual grading, which is however monotonous and time-consuming. Methods: We evaluated state-of-the-art deep learning-based methods for single cell macrophage classification and compared them against the performance of nine cytology experts and evaluated inter- and intra-observer variability. Additionally, we evaluated object detection methods on a novel data set of 17 completely annotated cytology whole slide images (WSI) containing 78,047 hemosiderophages. Resultsf: Our deep learning-based approach reached a concordance of 0.85, partially exceeding human expert concordance (0.68 to 0.86, $μ$=0.73, $σ$ =0.04). Intra-observer variability was high (0.68 to 0.88) and inter-observer concordance was moderate (Fleiss kappa = 0.67). Our object detection approach has a mean average precision of 0.66 over the five classes from the whole slide gigapixel image and a computation time of below two minutes. Conclusion: To mitigate the high inter- and intra-rater variability, we propose our automated object detection pipeline, enabling accurate, reproducible and quick EIPH scoring in WSI.

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Field Of Interest Proposal for Augmented Mitotic Cell Count: Comparison of two Convolutional Networks

Most tumor grading systems for human as for veterinary histopathology are based upon the absolute count of mitotic figures in a certain reference area of a histology slide. Since time for prognostication is limited in a diagnostic setting, the pathologist will often almost arbitrarily choose a certain field of interest assumed to have the highest mitotic activity. However, as mitotic figures are commonly very sparse on the slide and often have a patchy distribution, this poses a sampling problem which is known to be able to influence the tumor prognostication. On the other hand, automatic detection of mitotic figures can't yet be considered reliable enough for clinical application. In order to aid the work of the human expert and at the same time reduce variance in tumor grading, it is beneficial to assess the whole slide image (WSI) for the highest mitotic activity and use this as a reference region for human counting. For this task, we compare two methods for region of interest proposal, both based on convolutional neural networks (CNN). For both approaches, the CNN performs a segmentation of the WSI to assess mitotic activity. The first method performs a segmentation at the original image resolution, while the second approach performs a segmentation operation at a significantly reduced resolution, cutting down on processing complexity. We evaluate the approach using a dataset of 32 completely annotated whole slide images of canine mast cell tumors, where 22 were used for training of the network and 10 for test. Our results indicate that, while the overall correlation to the ground truth mitotic activity is considerably higher (0.94 vs. 0.83) for the approach based upon the fine resolution network, the field of interest choices are only marginally better. Both approaches propose fields of interest that contain a mitotic count in the upper quartile of respective slides.

cs.CV↗

Augmented Mitotic Cell Count using Field Of Interest Proposal

Histopathological prognostication of neoplasia including most tumor grading systems are based upon a number of criteria. Probably the most important is the number of mitotic figures which are most commonly determined as the mitotic count (MC), i.e. number of mitotic figures within 10 consecutive high power fields. Often the area with the highest mitotic activity is to be selected for the MC. However, since mitotic activity is not known in advance, an arbitrary choice of this region is considered one important cause for high variability in the prognostication and grading. In this work, we present an algorithmic approach that first calculates a mitotic cell map based upon a deep convolutional network. This map is in a second step used to construct a mitotic activity estimate. Lastly, we select the image segment representing the size of ten high power fields with the overall highest mitotic activity as a region proposal for an expert MC determination. We evaluate the approach using a dataset of 32 completely annotated whole slide images, where 22 were used for training of the network and 10 for test. We find a correlation of r=0.936 in mitotic count estimate.

cs.CV↗

Motion Artifact Detection in Confocal Laser Endomicroscopy Images

Confocal Laser Endomicroscopy (CLE), an optical imaging technique allowing non-invasive examination of the mucosa on a (sub)cellular level, has proven to be a valuable diagnostic tool in gastroenterology and shows promising results in various anatomical regions including the oral cavity. Recently, the feasibility of automatic carcinoma detection for CLE images of sufficient quality was shown. However, in real world data sets a high amount of CLE images is corrupted by artifacts. Amongst the most prevalent artifact types are motion-induced image deteriorations. In the scope of this work, algorithmic approaches for the automatic detection of motion artifact-tainted image regions were developed. Hence, this work provides an important step towards clinical applicability of automatic carcinoma detection. Both, conventional machine learning and novel, deep learning-based approaches were assessed. The deep learning-based approach outperforms the conventional approaches, attaining an AUC of 0.90.

cs.CV↗

Deep Denoising for Hearing Aid Applications

Reduction of unwanted environmental noises is an important feature of today's hearing aids (HA), which is why noise reduction is nowadays included in almost every commercially available device. The majority of these algorithms, however, is restricted to the reduction of stationary noises. In this work, we propose a denoising approach based on a three hidden layer fully connected deep learning network that aims to predict a Wiener filtering gain with an asymmetric input context, enabling real-time applications with high constraints on signal delay. The approach is employing a hearing instrument-grade filter bank and complies with typical hearing aid demands, such as low latency and on-line processing. It can further be well integrated with other algorithms in an existing HA signal processing chain. We can show on a database of real world noise signals that our algorithm is able to outperform a state of the art baseline approach, both using objective metrics and subject tests.

eess.AS↗

SlideRunner - A Tool for Massive Cell Annotations in Whole Slide Images

Large-scale image data such as digital whole-slide histology images pose a challenging task at annotation software solutions. Today, a number of good solutions with varying scopes exist. For cell annotation, however, we find that many do not match the prerequisites for fast annotations. Especially in the field of mitosis detection, it is assumed that detection accuracy could significantly benefit from larger annotation databases that are currently however very troublesome to produce. Further, multiple independent (blind) expert labels are a big asset for such databases, yet there is currently no tool for this kind of annotation available. To ease this tedious process of expert annotation and grading, we introduce SlideRunner, an open source annotation and visualization tool for digital histopathology, developed in close cooperation with two pathologists. SlideRunner is capable of setting annotations like object centers (for e.g. cells) as well as object boundaries (e.g. for tumor outlines). It provides single-click annotations as well as a blind mode for multi-annotations, where the expert is directly shown the microscopy image containing the cells that he has not yet rated.

cs.CV↗

A Guided Spatial Transformer Network for Histology Cell Differentiation

Identification and counting of cells and mitotic figures is a standard task in diagnostic histopathology. Due to the large overall cell count on histological slides and the potential sparse prevalence of some relevant cell types or mitotic figures, retrieving annotation data for sufficient statistics is a tedious task and prone to a significant error in assessment. Automatic classification and segmentation is a classic task in digital pathology, yet it is not solved to a sufficient degree. We present a novel approach for cell and mitotic figure classification, based on a deep convolutional network with an incorporated Spatial Transformer Network. The network was trained on a novel data set with ten thousand mitotic figures, about ten times more than previous data sets. The algorithm is able to derive the cell class (mitotic tumor cells, non-mitotic tumor cells and granulocytes) and their position within an image. The mean accuracy of the algorithm in a five-fold cross-validation is 91.45%. In our view, the approach is a promising step into the direction of a more objective and accurate, semi-automatized mitosis counting supporting the pathologist.

cs.CV↗

Automatic Classification of Cancerous Tissue in Laserendomicroscopy Images of the Oral Cavity using Deep Learning

Oral Squamous Cell Carcinoma (OSCC) is a common type of cancer of the oral epithelium. Despite their high impact on mortality, sufficient screening methods for early diagnosis of OSCC often lack accuracy and thus OSCCs are mostly diagnosed at a late stage. Early detection and accurate outline estimation of OSCCs would lead to a better curative outcome and an reduction in recurrence rates after surgical treatment. Confocal Laser Endomicroscopy (CLE) records sub-surface micro-anatomical images for in vivo cell structure analysis. Recent CLE studies showed great prospects for a reliable, real-time ultrastructural imaging of OSCC in situ. We present and evaluate a novel automatic approach for a highly accurate OSCC diagnosis using deep learning technologies on CLE images. The method is compared against textural feature-based machine learning approaches that represent the current state of the art. For this work, CLE image sequences (7894 images) from patients diagnosed with OSCC were obtained from 4 specific locations in the oral cavity, including the OSCC lesion. The present approach is found to outperform the state of the art in CLE image recognition with an area under the curve (AUC) of 0.96 and a mean accuracy of 88.3% (sensitivity 86.6%, specificity 90%).

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