Identifying temporally differentially expressed genes through functional principal components analysis
Biostatistics, ISSN: 1465-4644, Vol: 10, Issue: 4, Page: 667-679
2009
- 18Citations
- 33Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations18
- Citation Indexes18
- CrossRef18
- 18
- Captures33
- Readers33
- 33
Article Description
Time course gene microarray is an important tool to identify genes with differential expressions over time. Traditional analysis of variance (ANOVA) type of longitudinal investigation may not be applicable because of irregular time intervals and possible missingness due to contamination in microarray experiments. Functional principal components analysis is proposed to test hypotheses in the change of the mean curves. A permutation test under a mild assumption is used to make the method more robust. The proposed method outperforms the recently developed extraction of differential gene expression and a 2-way mixed effects ANOVA under reasonable gene expression models in simulation. Real data on transcriptional profiles of blood cells microarray from treated and untreated individuals were used to illustrate this method.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=74349089785&origin=inward; http://dx.doi.org/10.1093/biostatistics/kxp022; http://www.ncbi.nlm.nih.gov/pubmed/19602570; https://academic.oup.com/biostatistics/article-lookup/doi/10.1093/biostatistics/kxp022; https://dx.doi.org/10.1093/biostatistics/kxp022; https://academic.oup.com/biostatistics/article-abstract/10/4/667/233416?redirectedFrom=fulltext
Oxford University Press (OUP)
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