Hi, I have to analyze published scRNA-Seq data. Data are Chromium 10X on NovaSeq6000 and: for each sample I have forward (R1) in lane1 and lane2 (and hence two files) and reverse (R2) in lane1 and lane2 (and hence two files). Totally I have 4 files for sample. I have .fastq files. I usually analyze 10X scRNA-Seq data using Cellranger in single strand starting from the demultiplexing and ending with the alignment. It is the first time I have forward and reverse fastq files on multiple lanes and I don't know how to analyse them. Can anyone give me some hints on the analysis I have to do? Suggestions on tutorials, tools, papers about my task are more than welcome.
Thank you in advance
Are you still planning to use
cellranger
?No no it is the practice of the lab but it is not mandatory