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HMMvar-func:一种预测基因变异功能结果的新方法。

HMMvar-func: a new method for predicting the functional outcome of genetic variants.

作者信息

Liu Mingming, Watson Layne T, Zhang Liqing

机构信息

Department of Computer Science, Virginia Polytechnic Institute & State University, Blacksburg, USA.

Department of Mathematics, Virginia Polytechnic Institute & State University, Blacksburg, USA.

出版信息

BMC Bioinformatics. 2015 Oct 30;16:351. doi: 10.1186/s12859-015-0781-z.

Abstract

BACKGROUND

Numerous tools have been developed to predict the fitness effects (i.e., neutral, deleterious, or beneficial) of genetic variants on corresponding proteins. However, prediction in terms of whether a variant causes the variant bearing protein to lose the original function or gain new function is also needed for better understanding of how the variant contributes to disease/cancer. To address this problem, the present work introduces and computationally defines four types of functional outcome of a variant: gain, loss, switch, and conservation of function. The deployment of multiple hidden Markov models is proposed to computationally classify mutations by the four functional impact types.

RESULTS

The functional outcome is predicted for over a hundred thyroid stimulating hormone receptor (TSHR) mutations, as well as cancer related mutations in oncogenes or tumor suppressor genes. The results show that the proposed computational method is effective in fine grained prediction of the functional outcome of a mutation, and can be used to help elucidate the molecular mechanism of disease/cancer causing mutations. The program is freely available at http://bioinformatics.cs.vt.edu/zhanglab/HMMvar/download.php.

CONCLUSION

This work is the first to computationally define and predict functional impact of mutations, loss, switch, gain, or conservation of function. These fine grained predictions can be especially useful for identifying mutations that cause or are linked to cancer.

摘要

背景

已经开发了许多工具来预测基因变异对相应蛋白质的适应性影响(即中性、有害或有益)。然而,为了更好地理解变异如何导致疾病/癌症,还需要预测变异是否会使携带变异的蛋白质失去原有功能或获得新功能。为了解决这个问题,本研究引入并通过计算定义了变异的四种功能结果类型:功能获得、功能丧失、功能转换和功能保守。提出使用多个隐马尔可夫模型通过这四种功能影响类型对突变进行计算分类。

结果

对一百多个促甲状腺激素受体(TSHR)突变以及癌基因或肿瘤抑制基因中的癌症相关突变预测了功能结果。结果表明,所提出的计算方法在对突变功能结果的细粒度预测方面是有效的,可用于帮助阐明导致疾病/癌症的突变的分子机制。该程序可在http://bioinformatics.cs.vt.edu/zhanglab/HMMvar/download.php免费获取。

结论

本研究首次通过计算定义并预测了突变的功能影响,即功能丧失、功能转换、功能获得或功能保守。这些细粒度预测对于识别导致癌症或与癌症相关的突变可能特别有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0362/4628267/52a9accde366/12859_2015_781_Fig1_HTML.jpg

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