Does anyone have experience with taking the resulting .sam/.bam files from minimap2 and funneling them into a differential analysis package? Specifically, I am looking to take reads from Direct RNA sequencing on the Oxford Nanopore Technology MinION to something similar to DESeq2. I chose minimap2 because the parameters can be tailored to fit the noisy long-reads from the MinION. I was able to run minimap2 successfully, but from there I have hit a wall. I attempted to follow the document: https://bioc.ism.ac.jp/packages/2.14/bioc/vignettes/DESeq2/inst/doc/beginner.pdf
But when it comes to the sample table, I am confused as to how to find/generate it. Any help or advice for a first time RNA-seq analysis would be greatly appreciated.
Does anyone have experience with taking the resulting .sam/.bam files from minimap2 and funneling them into a differential analysis package? Specifically, I am looking to take reads from Direct RNA sequencing on the Oxford Nanopore Technology MinION to something similar to DESeq2. I chose minimap2 because the parameters can be tailored to fit the noisy long-reads from the MinION. I was able to run minimap2 successfully, but from there I have hit a wall. I attempted to follow the document: https://bioc.ism.ac.jp/packages/2.14/bioc/vignettes/DESeq2/inst/doc/beginner.pdf
But when it comes to the sample table, I am confused as to how to find/generate it. Any help or advice for a first time RNA-seq analysis would be greatly appreciated.