3,576 research outputs found
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
A cDNA Microarray Gene Expression Data Classifier for Clinical Diagnostics Based on Graph Theory
Despite great advances in discovering cancer molecular profiles, the proper application of microarray technology to routine clinical diagnostics is still a challenge. Current practices in the classification of microarrays' data show two main limitations: the reliability of the training data sets used to build the classifiers, and the classifiers' performances, especially when the sample to be classified does not belong to any of the available classes. In this case, state-of-the-art algorithms usually produce a high rate of false positives that, in real diagnostic applications, are unacceptable. To address this problem, this paper presents a new cDNA microarray data classification algorithm based on graph theory and is able to overcome most of the limitations of known classification methodologies. The classifier works by analyzing gene expression data organized in an innovative data structure based on graphs, where vertices correspond to genes and edges to gene expression relationships. To demonstrate the novelty of the proposed approach, the authors present an experimental performance comparison between the proposed classifier and several state-of-the-art classification algorithm
Motif Discovery through Predictive Modeling of Gene Regulation
We present MEDUSA, an integrative method for learning motif models of
transcription factor binding sites by incorporating promoter sequence and gene
expression data. We use a modern large-margin machine learning approach, based
on boosting, to enable feature selection from the high-dimensional search space
of candidate binding sequences while avoiding overfitting. At each iteration of
the algorithm, MEDUSA builds a motif model whose presence in the promoter
region of a gene, coupled with activity of a regulator in an experiment, is
predictive of differential expression. In this way, we learn motifs that are
functional and predictive of regulatory response rather than motifs that are
simply overrepresented in promoter sequences. Moreover, MEDUSA produces a model
of the transcriptional control logic that can predict the expression of any
gene in the organism, given the sequence of the promoter region of the target
gene and the expression state of a set of known or putative transcription
factors and signaling molecules. Each motif model is either a -length
sequence, a dimer, or a PSSM that is built by agglomerative probabilistic
clustering of sequences with similar boosting loss. By applying MEDUSA to a set
of environmental stress response expression data in yeast, we learn motifs
whose ability to predict differential expression of target genes outperforms
motifs from the TRANSFAC dataset and from a previously published candidate set
of PSSMs. We also show that MEDUSA retrieves many experimentally confirmed
binding sites associated with environmental stress response from the
literature.Comment: RECOMB 200
Pairwise gene GO-based measures for biclustering of high-dimensional expression data
Background: Biclustering algorithms search for groups of genes that share the same
behavior under a subset of samples in gene expression data. Nowadays, the biological
knowledge available in public repositories can be used to drive these algorithms to
find biclusters composed of groups of genes functionally coherent. On the other hand,
a distance among genes can be defined according to their information stored in Gene
Ontology (GO). Gene pairwise GO semantic similarity measures report a value for each
pair of genes which establishes their functional similarity. A scatter search-based
algorithm that optimizes a merit function that integrates GO information is studied in
this paper. This merit function uses a term that addresses the information through a GO
measure.
Results: The effect of two possible different gene pairwise GO measures on the
performance of the algorithm is analyzed. Firstly, three well known yeast datasets with
approximately one thousand of genes are studied. Secondly, a group of human
datasets related to clinical data of cancer is also explored by the algorithm. Most of
these data are high-dimensional datasets composed of a huge number of genes. The
resultant biclusters reveal groups of genes linked by a same functionality when the
search procedure is driven by one of the proposed GO measures. Furthermore, a
qualitative biological study of a group of biclusters show their relevance from a cancer
disease perspective.
Conclusions: It can be concluded that the integration of biological information
improves the performance of the biclustering process. The two different GO measures
studied show an improvement in the results obtained for the yeast dataset. However, if
datasets are composed of a huge number of genes, only one of them really improves
the algorithm performance. This second case constitutes a clear option to explore
interesting datasets from a clinical point of view.Ministerio de Economía y Competitividad TIN2014-55894-C2-
DNA Microarray Data Analysis: A New Survey on Biclustering
There are subsets of genes that have similar behavior under subsets of conditions, so we say that they coexpress, but behave independently under other subsets of conditions. Discovering such coexpressions can be helpful to uncover genomic knowledge such as gene networks or gene interactions. That is why, it is of utmost importance to make a simultaneous clustering of genes and conditions to identify clusters of genes that are coexpressed under clusters of conditions. This type of clustering is called biclustering.Biclustering is an NP-hard problem. Consequently, heuristic algorithms are typically used to approximate this problem by finding suboptimal solutions. In this paper, we make a new survey on biclustering of gene expression data, also called microarray data
Discovering gene association networks by multi-objective evolutionary quantitative association rules
In the last decade, the interest in microarray technology has exponentially increased due to its
ability to monitor the expression of thousands of genes simultaneously. The reconstruction of gene
association networks from gene expression profiles is a relevant task and several statistical
techniques have been proposed to build them. The problem lies in the process to discover which
genes are more relevant and to identify the direct regulatory relationships among them. We
developed a multi-objective evolutionary algorithm for mining quantitative association rules to deal
with this problem. We applied our methodology named GarNet to a well-known microarray data of
yeast cell cycle. The performance analysis of GarNet was organized in three steps similarly to the
study performed by Gallo et al. GarNet outperformed the benchmark methods in most cases in terms
of quality metrics of the networks, such as accuracy and precision, which were measured using
YeastNet database as true network. Furthermore, the results were consistent with previous
biological knowledge.Ministerio de Ciencia y Tecnología TIN2011-28956-C02-02Junta de Andalucía P11-TIC-752
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