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Dai, R.

Publications and source records attributed to Dai, R..

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csuWGCNA: a combination of signed and unsigned WGCNA to capture negative correlations

Network analysis helps us to understand how genes jointly affect biological functions. Weighted Gene Co-expression Network Analysis (WGCNA) is a frequently used method to build gene co-expression networks. WGCNA may be calculated with signed or unsigned correlations, with both methods having strengths and weaknesses, but both methods fail to capture weak and moderate negative correlations, which may be important in gene regulation. Combining the advantages and removing the disadvantages of both methods in one analysis would be desirable. In this study, we present a combination of signed and unsigned WGCNA (csuWGCNA), which combines the signed and unsigned methods and improves the detection of negative correlations. We applied csuWGCNA in 14 simulated datasets, six ground truth datasets and two large human brain datasets. Multiple metrics were used to evaluate csuWGCNA at gene pair and gene module levels. We found that csuWGCNA provides robust module detection and captures more negative correlations than the other methods, and is especially useful for non-coding RNA such as microRNA (miRNA) and long non-coding RNA (lncRNA). csuWGCNA enables detection of more informative modules with biological functions than signed or unsigned WGCNA, which enables discovery of novel gene regulation and helps interpretations in systems biology.

bioinformatics

Positional effects revealed in Illumina Methylation Array and the impact on analysis

With the evolution of rapid epigenetic research, Illumina Infinium HumanMethylation BeadChips have been widely used to study DNA methylation. However, in evaluating the accuracy of this method, we found that the commonly used Illumina HumanMethylation BeadChips are substantially affected by positional effects; the DNA samples location in a chip affects the measured methylation levels. We analyzed three HumanMethylation450 and three HumanMethylation27 datasets by using four methods to prove the existence of positional effects. Three datasets were analyzed further for technical replicate analysis or differential methylation CpG sites analysis. The pre- and post-correction comparisons indicate that the positional effects could alter the measured methylation values and downstream analysis results. Nevertheless, ComBat, linear regression and functional normalization could all be used to minimize such artifact. We recommend performing ComBat to correct positional effects followed by the correction of batch effects in data preprocessing as this procedure slightly outperforms the others. In addition, randomizing the sample placement should be a critical laboratory practice for using such experimental platforms. Code for our method is freely available at: https://github.com/ChuanJ/posibatch.

bioinformatics