25,548 research outputs found
Memory and information processing in neuromorphic systems
A striking difference between brain-inspired neuromorphic processors and
current von Neumann processors architectures is the way in which memory and
processing is organized. As Information and Communication Technologies continue
to address the need for increased computational power through the increase of
cores within a digital processor, neuromorphic engineers and scientists can
complement this need by building processor architectures where memory is
distributed with the processing. In this paper we present a survey of
brain-inspired processor architectures that support models of cortical networks
and deep neural networks. These architectures range from serial clocked
implementations of multi-neuron systems to massively parallel asynchronous ones
and from purely digital systems to mixed analog/digital systems which implement
more biological-like models of neurons and synapses together with a suite of
adaptation and learning mechanisms analogous to the ones found in biological
nervous systems. We describe the advantages of the different approaches being
pursued and present the challenges that need to be addressed for building
artificial neural processing systems that can display the richness of behaviors
seen in biological systems.Comment: Submitted to Proceedings of IEEE, review of recently proposed
neuromorphic computing platforms and system
In silico generation of novel, drug-like chemical matter using the LSTM neural network
The exploration of novel chemical spaces is one of the most important tasks
of cheminformatics when supporting the drug discovery process. Properly
designed and trained deep neural networks can provide a viable alternative to
brute-force de novo approaches or various other machine-learning techniques for
generating novel drug-like molecules. In this article we present a method to
generate molecules using a long short-term memory (LSTM) neural network and
provide an analysis of the results, including a virtual screening test. Using
the network one million drug-like molecules were generated in 2 hours. The
molecules are novel, diverse (contain numerous novel chemotypes), have good
physicochemical properties and have good synthetic accessibility, even though
these qualities were not specific constraints. Although novel, their structural
features and functional groups remain closely within the drug-like space
defined by the bioactive molecules from ChEMBL. Virtual screening using the
profile QSAR approach confirms that the potential of these novel molecules to
show bioactivity is comparable to the ChEMBL set from which they were derived.
The molecule generator written in Python used in this study is available on
request.Comment: in this version fixed some reference number
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