Changes between Version 9 and Version 10 of SOP/CallingVariantsRNAseq
- Timestamp:
- 08/16/17 12:28:53 (7 years ago)
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SOP/CallingVariantsRNAseq
v9 v10 18 18 To generate genome index files for STAR: 19 19 {{{ 20 '' Run this command within the "FirstPass" directory:'' '''''' 20 21 21 bsub STAR --runMode genomeGenerate --genomeDir /path/to/GenomeDir --genomeFastaFiles /path/to/genome/fasta1 /path/to/genome/fasta2 --sjdbGTFfile /path/to/GTF/FileName.gtf --sjdbOverhang 100 --runThreadN 8 22 22 }}} … … 28 28 To map: 29 29 {{{ 30 # Input format: fastq ; output format: SAM 30 '''''Run this command within the "FirstPass" directory'' 31 '''# Input format: fastq ; output format: SAM 31 32 bsub STAR --genomeDir /path/to/GenomeDir --readFilesIn /path/to/read1.fastq --outFileNamePrefix whateverPrefix --runThreadN 8