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1.
Biomed Opt Express ; 5(11): 3848-58, 2014 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-25426315

RESUMO

Single-view x-ray luminescence computed tomography (XLCT) imaging has short data collection time that allows non-invasively and fast resolving the three-dimensional (3-D) distribution of x-ray-excitable nanophosphors within small animal in vivo. However, the single-view reconstruction suffers from a severe ill-posed problem because only one angle data is used in the reconstruction. To alleviate the ill-posedness, in this paper, we propose a wavelet-based reconstruction approach, which is achieved by applying a wavelet transformation to the acquired singe-view measurements. To evaluate the performance of the proposed method, in vivo experiment was performed based on a cone beam XLCT imaging system. The experimental results demonstrate that the proposed method cannot only use the full set of measurements produced by CCD, but also accelerate image reconstruction while preserving the spatial resolution of the reconstruction. Hence, it is suitable for dynamic XLCT imaging study.

2.
Biomed Mater Eng ; 24(6): 3771-8, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25227093

RESUMO

Microarray technologies offer practical diagnostic tools for cancer detection. One great challenge is to identify salient genes from the high dimensionality of microarray data that can directly contribute to the symptom of cancer. Interactions among genes have been recognized to be fundamentally important for understanding biological function. This paper proposes an interacting gene selection method for cancer classification by identifying useful interacting genes. The method firstly evaluates the interactivity degree of each gene according to the intricate interrelation among genes by cooperative game analysis. Then genes are selected in a forward way by considering both interactivity and relevance characters. Experimental comparisons are carried out on four publicly available microarray data sets with three outstanding gene selection methods. Moreover a gene set enrichment analysis is also performed on the selected gene subset. The results show that the proposed method achieves better classification performance and enrichment score than other gene selection methods.


Assuntos
Biomarcadores Tumorais/metabolismo , Teoria dos Jogos , Proteínas de Neoplasias/metabolismo , Neoplasias/diagnóstico , Neoplasias/metabolismo , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Mapeamento de Interação de Proteínas/métodos , Diagnóstico por Computador/métodos , Perfilação da Expressão Gênica/métodos , Humanos , Proteínas de Neoplasias/genética , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
3.
J Biomed Inform ; 46(2): 252-8, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23124059

RESUMO

Microarray analysis is widely accepted for human cancer diagnosis and classification. However the high dimensionality of microarray data poses a great challenge to classification. Gene selection plays a key role in identifying salient genes from thousands of genes in microarray data that can directly contribute to the symptom of disease. Although various excellent selection methods are currently available, one common problem of these methods is that genes which have strong discriminatory power as a group but are weak as individuals will be discarded. In this paper, a new gene selection method is proposed for cancer diagnosis and classification by retaining useful intrinsic groups of interdependent genes. The primary characteristic of this method is that the relevance between each gene and target will be dynamically updated when a new gene is selected. The effectiveness of our method is validated by experiments on six publicly available microarray data sets. Experimental results show that the classification performance and enrichment score achieved by our proposed method is better than those of other selection methods.


Assuntos
Biologia Computacional/métodos , Perfilação da Expressão Gênica/métodos , Marcadores Genéticos/genética , Neoplasias/diagnóstico , Neoplasias/genética , Bases de Dados Genéticas , Feminino , Humanos , Teoria da Informação , Masculino , Análise de Sequência com Séries de Oligonucleotídeos , Reprodutibilidade dos Testes , Máquina de Vetores de Suporte
4.
IEEE Trans Image Process ; 21(5): 2770-85, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22311861

RESUMO

Recent advances in geopositioning mobile phones have made it possible for users to collect a large number of GPS trajectories by recording their location information. However, these mobile phones with built-in GPS devices usually record far more data than needed, which brings about both heavy data storage and a computationally expensive burden in the rendering process for a Web browser. To address this practical problem, we present a fast polygonal approximation algorithm in 2-D space for the GPS trajectory simplification under the so-called integral square synchronous distance error criterion in a linear time complexity. The underlying algorithm is designed and implemented using a bottom-up multiresolution method, where the input of polygonal approximation in the coarser resolution is the polygonal curve achieved in the finer resolution. For each resolution (map scale), priority-queue structure is exploited in graph construction to construct the initialized approximated curve. Once the polygonal curve is initialized, two fine-tune algorithms are employed in order to achieve the desirable quality level. Experimental results validated that the proposed algorithm is fast and achieves a better approximation result than the existing competitive methods.


Assuntos
Algoritmos , Sistemas de Informação Geográfica , Interpretação de Imagem Assistida por Computador/métodos , Imageamento Tridimensional/métodos , Armazenamento e Recuperação da Informação/métodos , Reconhecimento Automatizado de Padrão/métodos , Aumento da Imagem/métodos , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
5.
IEEE Trans Image Process ; 15(1): 169-77, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16435547

RESUMO

Optimal context quantizers for minimum conditional entropy can be constructed by dynamic programming in the probability simplex space. The main difficulty, operationally, is the resulting complex quantizer mapping function in the context space, in which the conditional entropy coding is conducted. To overcome this difficulty, we propose new algorithms for designing context quantizers in the context space based on the multiclass Fisher discriminant and the kernel Fisher discriminant (KFD). In particular, the KFD can describe linearly nonseparable quantizer cells by projecting input context vectors onto a high-dimensional curve, in which these cells become better separable. The new algorithms outperform the previous linear Fisher discriminant method for context quantization. They approach the minimum empirical conditional entropy context quantizer designed in the probability simplex space, but with a practical implementation that employs a simple scalar quantizer mapping function rather than a large lookup table.


Assuntos
Algoritmos , Compressão de Dados/métodos , Aumento da Imagem/métodos , Interpretação de Imagem Assistida por Computador/métodos , Processamento de Sinais Assistido por Computador , Simulação por Computador , Modelos Estatísticos
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