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Creating the DE object

NOTE: It may take a bit longer to load this exercise.

Using our smoc2 overexpression samples, create the DESeq2 object such that the design formula specifies the comparison of the expression differences between the fibrosis and normal samples. The metadata for the experiment is displayed below. We have the data read in with the samples in the same order for the smoc2 raw counts, reordered_smoc2_rawcounts, and the metadata, smoc2_metadata.

smoc2 metadata

This exercise is part of the course

RNA-Seq with Bioconductor in R

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Exercise instructions

  • Create a DESeq2 object called dds_smoc2 using the DESeqDataSetFromMatrix() function by specifying the arguments: countData, colData, and design.

  • Run the DESeq() function to estimate the size factors, calculate the dispersions, and perform the model fitting and testing.

Hands-on interactive exercise

Have a go at this exercise by completing this sample code.

# Create DESeq2 object
dds_smoc2 <- ___(___ = ___,
                 ___ = ___,
                 ___ = ~ condition)

# Run the DESeq2 analysis
___ <- ___(___)
Edit and Run Code