4.7 Article

iTTCA-RF: a random forest predictor for tumor T cell antigens

期刊

JOURNAL OF TRANSLATIONAL MEDICINE
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12967-021-03084-x

关键词

Tumor T cell antigens; Random forest; MRMD; Feature selection; Hybrid features

资金

  1. National Natural Science Foundation of China [61922020]
  2. Sichuan Provincial Science Fund for Distinguished Young Scholars [2021JDJQ0025]
  3. Special Science Foundation of Quzhou [2020D003]

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The study developed a predictor called iTTCA-RF for identifying tumor T cell antigens, which outperformed other latest models. The predictor showed satisfactory performance with balanced accuracy, specificity, and sensitivity values over cross-validation and independent tests. The online prediction server for iTTCA-RF is freely accessible online.
Background: Cancer is one of the most serious diseases threatening human health. Cancer immunotherapy represents the most promising treatment strategy due to its high efficacy and selectivity and lower side effects compared with traditional treatment. The identification of tumor T cell antigens is one of the most important tasks for antitumor vaccines development and molecular function investigation. Although several machine learning predictors have been developed to identify tumor T cell antigen, more accurate tumor T cell antigen identification by existing methodology is still challenging. Methods: In this study, we used a non-redundant dataset of 592 tumor T cell antigens (positive samples) and 393 tumor T cell antigens (negative samples). Four types feature encoding methods have been studied to build an efficient predictor, including amino acid composition, global protein sequence descriptors and grouped amino acid and peptide composition. To improve the feature representation ability of the hybrid features, we further employed a two-step feature selection technique to search for the optimal feature subset. The final prediction model was constructed using random forest algorithm. Results: Finally, the top 263 informative features were selected to train the random forest classifier for detecting tumor T cell antigen peptides. iTTCA-RF provides satisfactory performance, with balanced accuracy, specificity and sensitivity values of 83.71%, 78.73% and 88.69% over tenfold cross-validation as well as 73.14%, 62.67% and 83.61% over independent tests, respectively. The online prediction server was freely accessible at http://lab.malab.cn/similar to acy/iTTCA. Conclusions: We have proven that the proposed predictor iTTCA-RF is superior to the other latest models, and will hopefully become an effective and useful tool for identifying tumor T cell antigens presented in the context of major histocompatibility complex class I.

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