I updated some of the tools and the RNAseq workflow to handle single end reads. I did this on a use case basis for the PBTA Splice project in which I was able to get the workflow to run on a few single end read samples.
Let me know if any additional information is needed.
I updated some of the tools and the RNAseq workflow to handle single end reads. I did this on a use case basis for the PBTA Splice project in which I was able to get the workflow to run on a few single end read samples.
Let me know if any additional information is needed.