Preparation and characterization of magnetite (Fe3O4) nanoparticles By Sol-Gel method

The magnetite (Fe3O4) nanoparticles were successfully synthesized and annealed under vacuum at different temperature. The Fe3O4 nanoparticles prepared via sol-gel assisted method and annealed at 200-400ºC were characterized by Fourier Transformation Infrared Spectroscopy (FTIR), X-ray Diffraction spectra (XRD), Field Emission Scanning Electron Microscope (FESEM) and Atomic Force Microscopy (AFM). The XRD result indicate the presence of Fe3O4 nanoparticles, and the Scherer`s Formula calculated the mean particles size in range of 2-25 nm. The FESEM result shows that the morphologies of the particles annealed at 400ºC are more spherical and partially agglomerated, while the EDS result indicates the presence of Fe3O4 by showing Fe-O group of elements. AFM analyzed the 3D and roughness of the sample; the Fe3O4 nanoparticles have a minimum diameter of 79.04 nm, which is in agreement with FESEM result. In many cases, the synthesis of Fe3O4 nanoparticles using FeCl3 and FeCl2 has not been achieved, according to some literatures, but this research was able to obtained Fe3O4 nanoparticles base on the characterization results

Clustering Algorithms: Their Application to Gene Expression Data

Gene expression data hide vital information required to understand the biological process that takes place in a particular organism in relation to its environment. Deciphering the hidden patterns in gene expression data proffers a prodigious preference to strengthen the understanding of functional genomics. The complexity of biological networks and the volume of genes present increase the challenges of comprehending and interpretation of the resulting mass of data, which consists of millions of measurements; these data also inhibit vagueness, imprecision, and noise. Therefore, the use of clustering techniques is a first step toward addressing these challenges, which is essential in the data mining process to reveal natural structures and iden-tify interesting patterns in the underlying data. The clustering of gene expression data has been proven to be useful in making known the natural structure inherent in gene expression data, understanding gene functions, cellular processes, and subtypes of cells, mining useful information from noisy data, and understanding gene regulation. The other benefit of clustering gene expression data is the identification of homology, which is very important in vaccine design. This review examines the various clustering algorithms applicable to the gene expression data in order to discover and provide useful knowledge of the appropriate clustering technique that will guarantee stability and high degree of accuracy in its analysis procedure

Biclustering fMRI time series

Tese de mestrado, Ciência de Dados, Universidade de Lisboa, Faculdade de Ciências, 2020Biclustering é um método de análise que procura gerar clusters tendo em conta simultaneamente as linhas e as colunas de uma matriz de dados. Este método tem sido vastamente explorado em análise de dados genéticos. Apesar de diversos estudos reconhecerem as capacidades deste método de análise em outras áreas de investigação, as últimas duas décadas tem sido marcadas por um número elevado de estudos aplicados em dados genéticos e pela ausência de uma linha de investigação que explore as capacidades de biclustering fora desta área tradicional Esta tese segue pistas que sugerem potencial no uso de biclustering em dados de natureza espaço-temporal. Considerando o contexto particular das neurociências, esta tese explora as capacidades dos algoritmos de biclustering em extrair conhecimento das séries temporais geradas por técnicas de imagem por ressonância magnética funcional (fMRI). Eta tese propõe uma metodologia para avaliar a capacidade de algoritmos de biclustering em estudar dados fMRI, considerando tanto dados sintéticos como dados reais. Para avaliar estes algoritmos, usamos métricas de avaliação interna. Os nossos resultados discutem o uso de diversas estratégias de busca, revelando a superioridade de estratégias exaustivos para obter os biclusters mais homogéneos. No entanto, o elevado custo computacional de estratégias exaustivas ainda são um desafio e é necessário pesquisa adicional para a busca eficiente de biclusters no contexto de análise de dados fMRI. Propomos adicionalmente uma nova metodologia de análise de biclusters baseada em algoritmos de descoberta de padrões para determinar os padrões mais frequentes presentes nas soluções de biclustering geradas. Um bicluster não é mais que um hipervértice num hipergrafo . Extrair padrões frequentes numa solução de biclustering implica extrair os hipervértices mais significativos. Numa primeira abordagem, isto permite entender relações entre regiões do cérebro e traçar perfis temporais que métodos tradicionais de estudos de correlação não são capazes de detetar. Adicionalmente, o processo de gerar os biclusters permite filtrar ligações pouco interessantes, permitindo potencialmente gerar hipergrafos de forma eficiente. A questão final é o que podemos fazer com este conhecimento. Conhecer a relação entre regiões do cérebro é o objetivo central das neurociências. Entender as ligações entre regiões do cérebro para vários sujeitos permitem traçar perfis. Nesse caso, propomos uma metodologia para extrapolar biclusters para dados tridimensionais e efetuar triclustering. Adicionalmente, entender a ligação entre zonas cerebrais permite identificar doenças como a esquizofrenia, demência ou o Alzheimer. Este trabalho aponta caminhos para o uso de biclustering na análise de dados espaço-temporais, em particular em neurociências. A metodologia de avaliação proposta mostra evidências da eficácia do biclustering para encontrar padrões locais em dados de fMRI, embora mais trabalhos sejam necessários em relação à escalabilidade para promover a aplicação em cenários reais.The effectiveness of biclustering, simultaneous clustering of both rows and columns in a data matrix, has been primarily shown in gene expression data analysis. Furthermore, several researchers recognize its potentialities in other research areas. Nevertheless, the last two decades witnessed many biclustering algorithms targeting gene expression data analysis and a lack of consistent studies exploring the capacities of biclustering outside this traditional application domain. Following hints that suggest potentialities for biclustering on Spatiotemporal data, particularly in neurosciences, this thesis explores biclustering’s capacity to extract knowledge from fMRI time series. This thesis proposes a methodology to evaluate biclustering algorithms’ feasibility to study the fMRI signal, considering both synthetic and realworld fMRI datasets. In the absence of ground truth to compare bicluster solutions with a reference one, we used internal valuation metrics. Results discussing the use of different search strategies showed the superiority of exhaustive approaches, obtaining the most homogeneous biclusters. However, their high computational cost is still a challenge, and further work is needed for the efficient use of biclustering in fMRI data analysis. We propose a new methodology for analyzing biclusters based on performing pattern mining algorithms to determine the most frequent patterns present in the generated biclustering solutions. A bicluster is nothing more than a hyperlink in a hypergraph. Extracting frequent patterns in a biclustering solution implies extracting the most significant hyperlinks. In a first approach, this allows to understand relationships between regions of the brain and draw temporal profiles that traditional methods of correlation studies cannot detect. Additionally, the process of generating biclusters allows filtering uninteresting links, potentially allowing to generate hypergraphs efficiently. The final question is, what can we do with this knowledge. Knowing the relationship between brain regions is the central objective of neurosciences. Understanding the connections between regions of the brain for various subjects allows one to draw profiles. In this case, we propose a methodology to extrapolate biclusters to threedimensional data and perform triclustering. Additionally, understanding the link between brain zones allows identifying diseases like schizophrenia, dementia, or Alzheimer’s. This work pinpoints avenues for the use of biclustering in Spatiotemporal data analysis, in particular neurosciences applications. The proposed evaluation methodology showed evidence of biclustering’s effectiveness in finding local fMRI data patterns, although further work is needed regarding scalability to promote the application in real scenarios

MIClique: An Algorithm to Identify Differentially Coexpressed Disease Gene Subset from Microarray Data

Computational analysis of microarray data has provided an effective way to identify disease-related genes. Traditional disease gene selection methods from microarray data such as statistical test always focus on differentially expressed genes in different samples by individual gene prioritization. These traditional methods might miss differentially coexpressed (DCE) gene subsets because they ignore the interaction between genes. In this paper, MIClique algorithm is proposed to identify DEC gene subsets based on mutual information and clique analysis. Mutual information is used to measure the coexpression relationship between each pair of genes in two different kinds of samples. Clique analysis is a commonly used method in biological network, which generally represents biological module of similar function. By applying the MIClique algorithm to real gene expression data, some DEC gene subsets which correlated under one experimental condition but uncorrelated under another condition are detected from the graph of colon dataset and leukemia dataset

G-Tric: enhancing triclustering evaluation using three-way synthetic datasets with ground truth

Tese de mestrado, Ciência de Dados, Universidade de Lisboa, Faculdade de Ciências, 2020Three-dimensional datasets, or three-way data, started to gain popularity due to their increasing capacity to describe inherently multivariate and temporal events, such as biological responses, social interactions along time, urban dynamics, or complex geophysical phenomena. Triclustering, subspace clustering of three-way data, enables the discovery of patterns corresponding to data subspaces (triclusters) with values correlated across the three dimensions (observations _ features _ contexts). With an increasing number of algorithms being proposed, effectively comparing them with state-of-the-art algorithms is paramount.These comparisons are usually performed using real data, without a known ground-truth, thus limiting the assessments. In this context, we propose a synthetic data generator, G-Tric, allowing the creation of synthetic datasets with configurable properties and the possibility to plant triclusters. The generator is prepared to create datasets resembling real three-way data from biomedical and social data domains, with the additional advantage of further providing the ground truth (triclustering solution) as output. G-Tric can replicate real-world datasets and create new ones that match researchers’ needs across several properties, including data type (numeric or symbolic), dimension, and background distribution. Users can tune the patterns and structure that characterize the planted triclusters (subspaces) and how they interact (overlapping). Data quality can also be controlled by defining the number of missing values, noise, and errors. Furthermore, a benchmark of datasets resembling real data is made available, together with the corresponding triclustering solutions (planted triclusters) and generating parameters. Triclustering evaluation using G-Tric provides the possibility to combine both intrinsic and extrinsic metrics to compare solutions that produce more reliable analyses. A set of predefined datasets, mimicking widely used three-way data and exploring crucial properties was generated and made available, highlighting G-Tric’s potential to advance triclustering state-of-the-art by easing the process of evaluating the quality of new triclustering approaches. Besides reviewing the current state-of-the-art regarding triclustering approaches, comparison studies and evaluation metrics, this work also analyzes how the lack of frameworks to generate synthetic data influences existent evaluation methodologies, limiting the scope of performance insights that can be extracted from each algorithm. As well as exemplifying how the set of decisions made on these evaluations can impact the quality and validity of those results. Alternatively, a different methodology that takes advantage of synthetic data with ground truth is presented. This approach, combined with the proposal of an extension to an existing clustering extrinsic measure, enables to assess solutions’ quality under new perspectives

Gene regulatory network modelling with evolutionary algorithms -an integrative approach

Building models for gene regulation has been an important aim of Systems Biology over the past years, driven by the large amount of gene expression data that has become available. Models represent regulatory interactions between genes and transcription factors and can provide better understanding of biological processes, and means of simulating both natural and perturbed systems (e.g. those associated with disease). Gene regulatory network (GRN) quantitative modelling is still limited, however, due to data issues such as noise and restricted length of time series, typically used for GRN reverse engineering. These issues create an under-determination problem, with many models possibly fitting the data. However, large amounts of other types of biological data and knowledge are available, such as cross-platform measurements, knockout experiments, annotations, binding site affinities for transcription factors and so on. It has been postulated that integration of these can improve model quality obtained, by facilitating further filtering of possible models. However, integration is not straightforward, as the different types of data can provide contradictory information, and are intrinsically noisy, hence large scale integration has not been fully explored, to date. Here, we present an integrative parallel framework for GRN modelling, which employs evolutionary computation and different types of data to enhance model inference. Integration is performed at different levels. (i) An analysis of cross-platform integration of time series microarray data, discussing the effects on the resulting models and exploring crossplatform normalisation techniques, is presented. This shows that time-course data integration is possible, and results in models more robust to noise and parameter perturbation, as well as reduced noise over-fitting. (ii) Other types of measurements and knowledge, such as knock-out experiments, annotated transcription factors, binding site affinities and promoter sequences are integrated within the evolutionary framework to obtain more plausible GRN models. This is performed by customising initialisation, mutation and evaluation of candidate model solutions. The different data types are investigated and both qualitative and quantitative improvements are obtained. Results suggest that caution is needed in order to obtain improved models from combined data, and the case study presented here provides an example of how this can be achieved. Furthermore, (iii), RNA-seq data is studied in comparison to microarray experiments, to identify overlapping features and possibilities of integration within the framework. The extension of the framework to this data type is straightforward and qualitative improvements are obtained when combining predicted interactions from single-channel and RNA-seq datasets