Publications by authors named "Manolis Christodoulakis"

Epileptic seizure detection and prediction by using noninvasive measurements such as scalp EEG signals or invasive, intracranial recordings, has been at the heart of epilepsy studies for at least three decades. To this end, the most common approach has been to consider short-length recordings (several seconds to a few minutes) around a seizure, aiming to identify significant changes that occur before or during seizures. An inherent assumption in this approach is the presence of a relatively constant EEG activity in the interictal period, which is interrupted by seizure occurrence.

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It is well-established that both volume conduction and the choice of recording reference (montage) affect the correlation measures obtained from scalp EEG, both in the time and frequency domains. As a result, a number of correlation measures have been proposed aiming to reduce these effects. In our previous work, we have showed that scalp-EEG based functional brain networks in patients with epilepsy exhibit clear periodic patterns at different time scales and that these patterns are strongly correlated to seizure onset, particularly at shorter time scales (around 3 and 5 h), which has important clinical implications.

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Objective: This paper proposes supervised and unsupervised algorithms for automatic muscle artifact detection and removal from long-term EEG recordings, which combine canonical correlation analysis (CCA) and wavelets with random forests (RF).

Methods: The proposed algorithms first perform CCA and continuous wavelet transform of the canonical components to generate a number of features which include component autocorrelation values and wavelet coefficient magnitude values. A subset of the most important features is subsequently selected using RF and labelled observations (supervised case) or synthetic data constructed from the original observations (unsupervised case).

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We investigated the correlation of epileptic seizure onset times with long term EEG functional brain network properties. To do so, we constructed binary functional brain networks from long-term, multichannel electroencephalographic data recorded from nine patients with epilepsy. The corresponding network properties were quantified using the average network degree.

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Automatic detection and removal of muscle artifacts plays an important role in long-term scalp electroencephalography (EEG) monitoring, and muscle artifact detection algorithms have been intensively investigated. This paper proposes an algorithm for automatic muscle artifacts detection and removal using canonical correlation analysis (CCA) and wavelet transform (WT) in epochs from long-term EEG recordings. The proposed method first performs CCA analysis and then conducts wavelet decomposition on the canonical components within a specific frequency range and selects a subset of the wavelet coefficients for subsequent processing.

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Seizure detection and prediction studies using scalp- or intracranial-EEG measurements often focus on short-length recordings around the occurrence of the seizure, normally ranging between several seconds and up to a few minutes before and after the event. The underlying assumption in these studies is the presence of a relatively constant EEG activity in the interictal period, that is presumably interrupted by the occurrence of a seizure, at the time the seizure starts or slightly earlier. In this study, we put this assumption under test, by examining long-duration scalp EEG recordings, ranging between 22 and 72 hours, of five patients with epilepsy.

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We investigated functional epigenetic changes that occur in primary human T lymphocytes during entry into the cell cycle and mapped these at the single-nucleosome level by ChIP-chip on tiling arrays for chromosomes 1 and 6. We show that nucleosome loss and flanking active histone marks define active transcriptional start sites (TSSs). Moreover, these signatures are already set at many inducible genes in quiescent cells prior to cell stimulation.

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The number of segregating sites provides an indicator of the degree of DNA sequence variation that is present in a sample, and has been of great interest to the biological, pharmaceutical and medical professions. In this paper, we first provide linear- and expected-sublinear-time algorithms for finding all the segregating sites of a given set of DNA sequences. We also describe a data structure for tracking segregating sites in a set of sequences, such that every time the set is updated with the insertion of a new sequence or removal of an existing one, the segregating sites are updated accordingly without the need to re-scan the entire set of sequences.

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