Open wang950312 opened 5 years ago
Hi,
I am facing a similar situation. Did you have any progress on using the Velocyto pipeline with Illumina?
Thanks, Nithish
Turns out the SRA data used was from the 10x platform. I Used Cell Ranger count on the fastq file and performed a velocyto run on the resulting BAM file.
I' m very interested in your team' s project, but the data I had was seqenced by Illumina HiSeq2000 for per cell. I read the pipline and found that the folder structure more similar to the smart-seq platform: one sample have several cells same as one well have several cell. So could I apply your plpline on my data?