Open lahongxu opened 4 years ago
I have the same question. Can the author provide more example codes to get the correct input files? The current tutorial is not detailed enough. I also have difficulty in generating the refgene file with the correct format. Hope the authors can spend a bit more time to polish the protocol. Many thanks!
I generated metafile for 10x scRNA-seq data using R. What I did is to read in the barcode file for each sample (the files in /outs folder from cellranger output) and merge the barcode information with the condition and the other two columns as suggested by the tutorial. But the difficulty I met is, since our data has 80,000+ cells, the SCATS count step generated 80,000+ .sh files to run. I tried one .sh file today and found it took more than 5 hours to complete one job. Then having 80,000 jobs all completed seems to be an impossible task... I am not sure if I did this correctly.
I generated metafile for 10x scRNA-seq data using R. What I did is to read in the barcode file for each sample (the files in /outs folder from cellranger output) and merge the barcode information with the condition and the other two columns as suggested by the tutorial. But the difficulty I met is, since our data has 80,000+ cells, the SCATS count step generated 80,000+ .sh files to run. I tried one .sh file today and found it took more than 5 hours to complete one job. Then having 80,000 jobs all completed seems to be an impossible task... I am not sure if I did this correctly.
@ziyili20 I tried your methods and it works on my side too. Thanks! But I have the same issue re: the running time...
Hi, I am going to use SCATS to analyze 10x scRNA-seq data. After running cellranger, I can only get one bam file containing many cells. How can I generate metafile for SCATS step2? Can you give an example for it?