In this paper we describe a fast and accurate pipeline for real-time face recognition that is based on a convolutional neural network (CNN) and requires only moderate computational resources. After training the CNN on a desktop PC we employed a Raspberry Pi, model B, for the classi cation procedure. Here, we reached a performance of approximately 2 frames per second and more than 97% recognition accuracy. The proposed approach outperforms all of OpenCV’s algorithms with respect to both accuracy and speed and shows the applicability of recent deep learning techniques to hardware with limited computational performance.
Makale: Autonomous Vehicles Need Experimental Ethics: Are We Ready for Utilitarian Cars?
The wide adoption of self-driving, Autonomous Vehicles (AVs) promises to dramatically reduce the number of traffic accidents. Some accidents, though, will be inevitable, because some situations will require AVs to choose the lesser of two evils. For example, running over a pedestrian on the road or a passer-by on the side; or choosing whether to run over a group of pedestrians or to sacrifice the passenger by driving into a wall. It is a formidable challenge to define the algorithms that will guide AVs confronted with such moral dilemmas. In particular, these moral algorithms will need to accomplish three potentially incompatible objectives: being consistent, not causing public outrage, and not discouraging buyers. We argue to achieve these objectives, manufacturers and regulators will need psychologists to apply the methods of experimental ethics to situations involving AVs and unavoidable harm. To illustrate our claim, we report three surveys showing that laypersons are relatively comfortable with utilitarian AVs, programmed to minimize the death toll in case of unavoidable harm. We give special attention to whether an AV should save lives by sacrificing its owner, and provide insights into (i) the perceived morality of this self-sacrifice, (ii) the willingness to see this self-sacrifice being legally enforced, (iii) the expectations that AVs will be programmed to self-sacrifice, and (iv) the willingness to buy self-sacrificing AVs.
Ankara Deep Learning – Derin Öğrenme Etkinliği
13 Ekim 2015 saat 19:00’da Hacettepe Teknokent Safir Bloklar Konferans Salonunda gerçekleştirdiğimiz Derin Öğrenme etkinliğinin video ve sunum dosyasına aşağıdan erişebilirsiniz.
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derin_ogrenme_linked_13.10.2015.pdf
Etkinlikten Resimler
Makale: Deep Learning as an Opportunity in Virtual Screening
Deep learning excels in vision and speech applications where it pushed the stateof-the-art to a new level. However its impact on other fields remains to be shown. The Merck Kaggle challenge on chemical compound activity was won by Hinton’s group with deep networks. This indicates the high potential of deep learning in drug design and attracted the attention of big pharma. However, the unrealistically small scale of the Kaggle dataset does not allow to assess the value of deep learning in drug target prediction if applied to in-house data of pharmaceutical companies. Even a publicly available drug activity data base like ChEMBL is magnitudes larger than the Kaggle dataset. ChEMBL has 13 M compound descriptors, 1.3 M compounds, and 5 k drug targets, compared to the Kaggle dataset with 11 k descriptors, 164 k compounds, and 15 drug targets.
On the ChEMBL database, we compared the performance of deep learning to seven target prediction methods, including two commercial predictors, three predictors deployed by pharma, and machine learning methods that we could scale to this dataset. Deep learning outperformed all other methods with respect to the area under ROC curve and was significantly better than all commercial products. Deep learning surpassed the threshold to make virtual compound screening possible and has the potential to become a standard tool in industrial drug design.
Makale: Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
Knowing the sequence specificities of DNA- and RNA-binding proteins is essential for developing models of the regulatory processes in biological systems and for identifying causal disease variants. Here we show that sequence specificities can be ascertained from experimental data with ‘deep learning’ techniques, which offer a scalable, flexible and unified computational approach for pattern discovery. Using a diverse array of experimental data and evaluation metrics, we find that deep learning outperforms other state-of-the-art methods, even when training on in vitro data and testing on in vivo data. We call this approach DeepBind and have built a stand-alone software tool that is fully automatic and handles millions of sequences per experiment. Specificities determined by DeepBind are readily visualized as a weighted ensemble of position weight matrices or as a ‘mutation map’ that indicates how variations affect binding within a specific sequence.