Hi All,
I'm new to RNA-Seq and Bioinformatics. We have done a RNA-Seq study using Illumina Hi-Seq (paired-end, 90bp reads) on two cell types.
I have managed to remove the adapters, trim low quality reads and remove reads < 50bp (Trim Galore). I have then mapped them (TopHat-v2.0.8b) and assembled the mapped reads (Cufflinks). I then merged the reads (Cuffmerge) followed by differential gene analyses (CummeRbund).
When I generated a heatmap of the differentially expressed genes, I came across three instances of NA corresponding to a XLOC ID!
1) I'm not sure what this means?
2) Is there a way to remove these entries from the .db database and hence from the heatmap assuming that its something useless?
Any help would be greatly appreciated!
Cheers!
I'm new to RNA-Seq and Bioinformatics. We have done a RNA-Seq study using Illumina Hi-Seq (paired-end, 90bp reads) on two cell types.
I have managed to remove the adapters, trim low quality reads and remove reads < 50bp (Trim Galore). I have then mapped them (TopHat-v2.0.8b) and assembled the mapped reads (Cufflinks). I then merged the reads (Cuffmerge) followed by differential gene analyses (CummeRbund).
When I generated a heatmap of the differentially expressed genes, I came across three instances of NA corresponding to a XLOC ID!
1) I'm not sure what this means?
2) Is there a way to remove these entries from the .db database and hence from the heatmap assuming that its something useless?
Any help would be greatly appreciated!
Cheers!