Classification of chemically modified red blood cells in microflow using machine learning video analysis.

We classify native and chemically modified red blood cells with an AI based video classifier. Using TensorFlow video analysis enables us to capture not only the morphology of the cell but also the trajectories of motion of individual red blood cells and their dynamics. We chemically modify cells in three different ways to model different pathological conditions and obtain classification accuracies for all three classification tasks of more than 90% between native and modified cells. Unlike standard cytometers that are based on immunophenotyping our microfluidic cytometer allows to rapidly categorize cells without any fluorescence labels simply by analysing the shape and flow of red blood cells.

Proof of concept evaluation of the electroencephalophone as a discriminator between wakefulness and general anaesthesia.

BACKGROUND: Depth of anaesthesia (DOA) monitors based on the electroencephalogram (EEG) are commonly used in anaesthetic practice. Their technology relies on mathematical analysis of the EEG waveform, generally resulting in a number which corresponds to anaesthetic depth. We have created a novel method of interpreting the EEG, which retains its underlying complexity. This method consists of turning the EEG into a sound: the electroencephalophone (EEP). METHODS: In a pilot study, we recorded awake and anaesthetized EEGs from six patients. We transformed each EEG into an audio signal using a ring buffer with a write frequency of 1 kHz and a read frequency of 48 kHz, thus elevating all output frequencies by a factor of 48. In essence, the listener hears the previous 12 s of EEG data compressed into 250 ms, updated every 250 ms. From these data, we generated a bank of 5 s audio clips, which were then used to train and test a sample of 23 anaesthetists. RESULTS: After training, 21 of the 23 anaesthetists were able to use the EEP to correctly identify the conscious state of >5 of 10 randomly selected patients (P<0.001). The median score was 8 out of 10, with an inter-quartile range of 7-9. CONCLUSIONS: The EEP shows promise as a DOA monitor. However, extensive validation would be required in a variety of clinical settings before it could be accepted into mainstream clinical practice.

Synaptic modifications depend on synapse location and activity: a biophysical model of STDP.

In spike-timing-dependent plasticity (STDP) the synapses are potentiated or depressed depending on the temporal order and temporal difference of the pre- and post-synaptic signals. We present a biophysical model of STDP which assumes that not only the timing, but also the shapes of these signals influence the synaptic modifications. The model is based on a Hebbian learning rule which correlates the NMDA synaptic conductance with the post-synaptic signal at synaptic location as the pre- and post-synaptic quantities. As compared to a previous paper [Saudargiene, A., Porr, B., Worgotter, F., 2004. How the shape of pre- and post-synaptic signals can influence stdp: a biophysical model. Neural Comp.], here we show that this rule reproduces the generic STDP weight change curve by using real neuronal input signals and combinations of more than two (pre- and post-synaptic) spikes. We demonstrate that the shape of the STDP curve strongly depends on the shape of the depolarising membrane potentials, which induces learning. As these potentials vary at different locations of the dendritic tree, model predicts that synaptic changes are location dependent. The model is extended to account for the patterns of more than two spikes of the pre- and post-synaptic cells. The results show that STDP weight change curve is also activity dependent.

Isotropic sequence order learning using a novel linear algorithm in a closed loop behavioural system.

In this article, we present an isotropic algorithm for sequence order learning. Its central goal is to learn the causal relation between two (or more) inputs in order to react to the earliest incoming signal after successful learning (like in typical classical conditioning situations). We implement this algorithm in a behaving system (a robot) thereby creating a closed loop situation where the learner's actions influence its own sensor inputs to the end of creating an autonomous agent. Autonomous behaviour implies that learning goals are internally defined within the organism's capabilities. Standard learning models for sequence learning (e.g. temporal difference (TD)-learning) need an externally defined reward. This, however, is in conflict with the requirement of an implicitly defined internal goal in autonomous behaviour. Therefore, in this study we present a system in which the external reward is replaced by a reflex loop. This loop explicitly includes the environment. Every reflex loop has the inherent disadvantage, which is that its re-actions occur each time just after a reflex-eliciting sensor event and thus 'too late'. However, a reflex can serve as the internal reference for sequence order learning, which has the task of eliminating this disadvantage by creating earlier anticipatory actions. In our system learning is achieved by modifying synaptic weights of a linear neuron with a correlation based learning rule which involves the derivative of the neuron's output. All input lines are entirely isotropic. The synaptic weight change curve of this rule is strongly related to the temporal Hebb learning rule, which was found in spike timing experiments. We find that after learning the reflex loop is replaced in functional terms with an earlier anticipatory action (and pathway). In addition, we observed that the synaptic weights stabilise as soon as the reflex remains silent.

How to "hear" visual disparities: real-time stereoscopic spatial depth analysis using temporal resonance.

In a stereoscopic system, both eyes or cameras have a slightly different view. As a consequence, small variations between the projected images exist ('disparities') which are spatially evaluated in order to retrieve depth information (Sanger 1988; Fleet et al. 1991). A strong similarity exists between the analysis of visual disparities and the determination of the azimuth of a sound source (Wagner and Frost 1993). The direction of the sound is thereby determined from the temporal delay between the left and right ear signals (Konishi and Sullivan 1986). Similarly, here we transpose the spatially defined problem of disparity analysis into the temporal domain and utilize two resonators implemented in the form of causal (electronic) filters to determine the disparity as local temporal phase differences between the left and right filter responses. This approach permits real-time analysis and can be solved analytically for a step function contrast change, which is an important case in all real-world applications. The proposed theoretical framework for spatial depth retrieval directly utilizes a temporal algorithm borrowed from auditory signal analysis. Thus, the suggested similarity between the visual and the auditory system in the brain (Wagner and Frost 1993) finds its analogy here at the algorithmical level. We will compare the results from the temporal resonance algorithm with those obtained from several other techniques like cross-correlation or spatial phase-based disparity estimation showing that the novel algorithm achieves performances similar to the 'classical' approaches using much lower computational resources.