my_singcell

This is a Split-seq Scell Data analysis method. This pipeline can process the over 20000 cells in 3 days. http://science.sciencemag.org/content/360/6385/176.full

##Useage pipeline:

  1. first step:

       files perpare: raw fastq files and barcode file
       change your paire-end fastq files name to R1.fastq(R1) and R2.fastq(R2)
    
  2. then run:

     init.sh to initialize the directy and environment.