|
|
|
|
LEADER |
01426nam a2200169Ia 4500 |
001 |
10.1093-BIOINFORMATICS-BTY203 |
008 |
220425s2018 CNT 000 0 und d |
020 |
|
|
|a 13674803 (ISSN)
|
245 |
1 |
0 |
|a methylGSA: a Bioconductor package and Shiny app for DNA methylation data length bias adjustment in gene set testing
|
260 |
|
0 |
|b Oxford University Press
|c 2018
|
856 |
|
|
|z View Fulltext in Publisher
|u https://doi.org/10.1093/BIOINFORMATICS/BTY203
|
520 |
3 |
|
|a Motivation: An important downstream analysis following differential expression from RNA sequencing (RNA-Seq) or DNA methylation analysis is the gene set testing to relate significant genes or CpGs to known biological properties. However, the traditional gene set testing approaches result in biased P-values due to the difference in gene length. Existing methods accounting for length bias were primarily developed for RNA-Seq data. For DNA methylation data profiled using the Illumina arrays, separate methods adjusting for the number of CpGs instead of gene length are necessary. Results: We developed methylGSA, a Bioconductor package for gene set testing in DNA methylation data. Our accompanying Shiny app provides an interactive way of accessing functions and visualizing the results in methylGSA package. © The Author(s) 2018.
|
650 |
0 |
4 |
|a article
|
650 |
0 |
4 |
|a DNA methylation
|
700 |
1 |
|
|a Kuan, P.F.
|e author
|
700 |
1 |
|
|a Ren, X.
|e author
|
773 |
|
|
|t Bioinformatics
|