Hi,
I am new to this forum and also to NGS data analysis. May I know if it is possible to analyse RNA variants from whole transcriptome/RNA sequencing (single end reads)? If so, I would appreciate if you could suggest appropriate literature/tools to carry out the analysis.
Thank you.
I am new to this forum and also to NGS data analysis. May I know if it is possible to analyse RNA variants from whole transcriptome/RNA sequencing (single end reads)? If so, I would appreciate if you could suggest appropriate literature/tools to carry out the analysis.
Thank you.