DESeq2

A basic task in the analysis of count data from RNA-seq is the detection of differentially expressed genes. The count data are presented as a table which reports, for each sample, the number of sequence fragments that have been assigned to each gene. Analogous data also arise for other assay types, including comparative ChIP-Seq, HiC, shRNA screening, and mass spectrometry.

An important analysis question is the quantification and statistical inference of systematic changes between conditions, as compared to within-condition variability. The package DESeq2 provides methods to test for differential expression by use of negative binomial generalized linear models; the estimates of dispersion and logarithmic fold changes incorporate data-driven prior distributions.

Love MI, Huber W, Anders S (2014). “Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.” Genome Biology, 15, 550. doi:10.1186/s13059-014-0550-8.


1. Users can upload the matrix of count data in .txt format to run DESeq2 analysis against selected tissues. For example, User can upload the fpkm matrix of DoGs with disease samples and identify differentially expressed DoGs between them.
Select Tissue
Upload files Download the example file
2. Users can select two tissue to run DESeq2 analysis against selected tissues.
Select the first Tissue
Select the second Tissue