4.7 Article

Ranking analysis for identifying differentially expressed genes

Journal

GENOMICS
Volume 97, Issue 5, Pages 326-329

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygeno.2011.03.002

Keywords

Microarray; Ranking analysis; Differentially expressed genes

Funding

  1. Natural Science Foundation of China [60973094, 61070121]
  2. Postdoctoral Science Foundation of China [20100481149]
  3. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [10KJB520006]

Ask authors/readers for more resources

Microarrays allow researchers to examine the expression of thousands of genes simultaneously. However, identification of genes differentially expressed in microarray experiments is challenging. With an optimal test statistic, we rank genes and estimate a threshold above which genes are considered to be differentially expressed genes (DE). This overcomes the embarrassing shortcoming of many statistical methods to determine the cut-off values in ranking analysis. Experiments demonstrate that our method is a good performance and avoids the problems with graphical examination and multiple hypotheses testing that affect alternative approaches. Comparing to those well known methods, our method is more sensitive to data sets with small differentially expressed values and not biased in favor of data sets based on certain distribution models. (C) 2011 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
Article Biotechnology & Applied Microbiology

MetaAc4C: A multi-module deep learning framework for accurate prediction of N4-acetylcytidine sites based on pre-trained bidirectional encoder representation and generative adversarial networks

Zutan Li, Bingbing Jin, Jingya Fang

Summary: In this study, we propose MetaAc4C, an advanced deep learning model for accurate identification of N4-acetylcytidine (ac4C) sites using pre-trained BERT and various optimization techniques. By adapting generative adversarial networks to address data imbalance and augmenting training RNA samples, our model outperforms existing methods in terms of ACC, MCC, and AUROC.

GENOMICS (2024)