I am new in the area of single cell RNA seq data analysis.I have 50 fastq files for a single sample from the Smart-seq2 platform.
I would like to generate a count matrix of expression for these files.
I did not find any example to process smart-seq2 data from the tutorial
Hello,
I am new in the area of single cell RNA seq data analysis.I have 50 fastq files for a single sample from the Smart-seq2 platform. I would like to generate a count matrix of expression for these files. I did not find any example to process smart-seq2 data from the tutorial
http://bioinf.wehi.edu.au/scPipe/
Is it posible to use scPipe for Smart-seq2?
Thank you very much.
Best regards Arshiya