Biodesign Institute

About: Biodesign Institute is a based out in . It is known for research contribution in the topics: Combretastatin & Mass spectrometry. The organization has 202 authors who have published 498 publications receiving 38570 citations.

MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment

Abstract: With its theoretical basis firmly established in molecular evolutionary and population genetics, the comparative DNA and protein sequence analysis plays a central role in reconstructing the evolutionary histories of species and multigene families, estimating rates of molecular evolution, and inferring the nature and extent of selective forces shaping the evolution of genes and genomes. The scope of these investigations has now expanded greatly owing to the development of high-throughput sequencing techniques and novel statistical and computational methods. These methods require easy-to-use computer programs. One such effort has been to produce Molecular Evolutionary Genetics Analysis (MEGA) software, with its focus on facilitating the exploration and analysis of the DNA and protein sequence variation from an evolutionary perspective. Currently in its third major release, MEGA3 contains facilities for automatic and manual sequence alignment, web-based mining of databases, inference of the phylogenetic trees, estimation of evolutionary distances and testing evolutionary hypotheses. This paper provides an overview of the statistical methods, computational tools, and visual exploration modules for data input and the results obtainable in MEGA.

Efficient Feature Selection via Analysis of Relevance and Redundancy

Abstract: Feature selection is applied to reduce the number of features in many applications where data has hundreds or thousands of features. Existing feature selection methods mainly focus on finding relevant features. In this paper, we show that feature relevance alone is insufficient for efficient feature selection of high-dimensional data. We define feature redundancy and propose to perform explicit redundancy analysis in feature selection. A new framework is introduced that decouples relevance analysis and redundancy analysis. We develop a correlation-based method for relevance and redundancy analysis, and conduct an empirical study of its efficiency and effectiveness comparing with representative methods.

A sensitive period for the development of the central auditory system in children with cochlear implants: implications for age of implantation.

Abstract: ObjectiveThe aim of the present experiment was to assess the consequences of cochlear implantation at different ages on the development of the human central auditory system.DesignOur measure of the maturity of central auditory pathways was the latency of the P1 cortical auditory evoked potential. Be

Short telomeres are a risk factor for idiopathic pulmonary fibrosis

Abstract: Idiopathic interstitial pneumonias (IIPs) have a progressive and often fatal course, and their enigmatic etiology has complicated approaches to effective therapies. Idiopathic pulmonary fibrosis (IPF) is the most common of IIPs and shares with IIPs an increased incidence with age and unexplained scarring in the lung. Short telomeres limit tissue renewal capacity in the lung and germ-line mutations in telomerase components, hTERT and hTR, underlie inheritance in a subset of families with IPF. To examine the hypothesis that short telomeres contribute to disease risk in sporadic IIPs, we recruited patients who have no family history and examined telomere length in leukocytes and in alveolar cells. To screen for mutations, we sequenced hTERT and hTR. We also reviewed the cases for features of a telomere syndrome. IIP patients had shorter leukocyte telomeres than age-matched controls (P < 0.0001). In a subset (10%), IIP patients had telomere lengths below the first percentile for their age. Similar to familial cases with mutations, IPF patients had short telomeres in alveolar epithelial cells (P < 0.0001). Although telomerase mutations were rare, detected in 1 of 100 patients, we identified a cluster of individuals (3%) with IPF and cryptogenic liver cirrhosis, another feature of a telomere syndrome. Short telomeres are thus a signature in IIPs and likely play a role in their age-related onset. The clustering of cryptogenic liver cirrhosis with IPF suggests that the telomere shortening we identify has consequences and can contribute to what appears clinically as idiopathic progressive organ failure in the lung and the liver.