Author Archives: P.T.R. Rupprecht

Open access 3D electron microscopy datasets of brains

One of the coolest technical developments in neuroscience during the last decade has been driven by 3D electron microscopy (3D EM). This allowed to cut large junks of small brains (or small junks of big brains) into 8-50 nm thick … Continue reading

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How well do CNNs for spike detection generalize to unseen datasets?

Some time ago, Stephan Gerhard and I have used a convolutional neural network (CNN) to detect neuronal spikes from calcium imaging data. (I have mentioned this before, here, here, and on Github.) This method is covered by the spikefinder paper … Continue reading

Posted in Calcium Imaging, Data analysis, machine learning, Neuronal activity | Tagged , , , , , , | Leave a comment

A list of cognitive biases

There are a handful of cognitive biases that are well-known to most scientists: confirmation bias, the Dunning-Kruger effect, the hindsight bias, the recency effect, the planning fallacy, loss aversion, etc.. Although they should not be taken as universal laws (for example, … Continue reading

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Springtime for two-photon microscopy

Today, the fields and forests around Basel are full of flowers that try to disseminate their pollen. Fixed pollen are, apart from sub-diffraction beads and the convallaria rhizome, one of the most commonly used test/reference samples for fluorescence microscopy. This … Continue reading

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Layer-wise decorrelation in deep-layered artificial neuronal networks

The most commonly used deep networks are purely feed-forward nets. The input is passed to layers 1, 2, 3, then at some point to the final layer (which can be 10, 100 or even 1000 layers away from the input).  … Continue reading

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Understanding style transfer

‘Style transfer’ is a method based on deep networks which extracts the style of a painting or picture in order to transfer it to a second picture. For example, the style of a butterfly image (left) is transferred to the … Continue reading

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Can two-photon scanning be too fast?

The following back-of-the-envelope calculations do not lead to any useful result, but you might be interesting in reading through them if you want to get a better understanding of what happens during two-photon excitation microscopy. The basic idea of two-photon microscopy … Continue reading

Posted in Imaging, Microscopy | Tagged , , , , | 8 Comments