مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

47
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

23
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Chronic Obstructive Pulmonary Disease: Novel Genes Detection with Penalized Logistic Regression

Pages

  203-211

Abstract

 Objective: This study aimed to introduce novel techniques for identifying the genes associated with developing chronic obstructive pulmonary disease (COPD) and to prioritize COPD candidate genes using regression methods. Materials and Methods: This is a secondary analysis of the data from an experimental study. We used penalized logistic regressions with three different types of penalties included least absolute shrinkage and selection operator (LASSO), minimax concave penalty (MCP), and smoothly clipped absolute deviation (SCAD). The models were trained using genome-wide expression profiling to define gene networks relevant to the COPD stages. A 10-fold cross-validation scheme was used to evaluate the performance of the methods. In addition, we validate our results by the external validity approach. We reported the sensitivity, specificity, and area under curve (AUC) of the models. Results: There were 21, 22, and 18 significantly associated genes for LASSO, SCAD, and MCP models, respectively. The most statistically conservative method (detecting less significant features) was MCP detected 18 genes that were all detected by the other two approaches. The most appropriate approach was a SCAD penalized logistic regression (AUC= 96. 26, sensitivity= 94. 2, specificity= 86. 96). In this study, we have a common panel of 18 genes in all three models that show a significant positive and negative correlation with COPD, in which RNF130, STX6, PLCB1, CACNA1G, LARP4B, LOC100507634, SLC38A2, and STIM2 showed the odds ratio (OR) more than 1. However, there was a slight difference between penalized methods. Conclusion: Regularization solves the serious dimensionality problem in using this kind of regression. More exploration of how these genes affect the outcome and mechanism is possible more quickly in this manner. The regression-based approaches we present could apply to overcoming this issue.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    GOHARI, KIMIYA, KAZEMNEJAD, ANOSHIRVAN, MOSTAFAEI, SHAYAN, SABERI, SAMANEH, & SHEIDAEI, ALI. (2023). Chronic Obstructive Pulmonary Disease: Novel Genes Detection with Penalized Logistic Regression. CELL JOURNAL (YAKHTEH), 25(3), 203-211. SID. https://sid.ir/paper/1038193/en

    Vancouver: Copy

    GOHARI KIMIYA, KAZEMNEJAD ANOSHIRVAN, MOSTAFAEI SHAYAN, SABERI SAMANEH, SHEIDAEI ALI. Chronic Obstructive Pulmonary Disease: Novel Genes Detection with Penalized Logistic Regression. CELL JOURNAL (YAKHTEH)[Internet]. 2023;25(3):203-211. Available from: https://sid.ir/paper/1038193/en

    IEEE: Copy

    KIMIYA GOHARI, ANOSHIRVAN KAZEMNEJAD, SHAYAN MOSTAFAEI, SAMANEH SABERI, and ALI SHEIDAEI, “Chronic Obstructive Pulmonary Disease: Novel Genes Detection with Penalized Logistic Regression,” CELL JOURNAL (YAKHTEH), vol. 25, no. 3, pp. 203–211, 2023, [Online]. Available: https://sid.ir/paper/1038193/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button