#!/bin/bash
# run this script before running any submission scripts!
# this script allows you to use samtools, ngstools, etc.

## Do not change this section of code unless you want to change software versions!
# within an interactive node (type "bsub -Is bash" to get to one), 
# you can see the list of available software versions by typing "module avail"
module load FastQC-0.11.2
module load samtools-0.1.19
module load ngsutils-0.5.7
module load STAR/2.7.1a
module load python/2.7.9                               # Loading python 2 is necessary because attempting to run with python 3 will lead to import errors at the HTSeq step.
STARFLAGS="--readFilesCommand zcat"
genomeDirSTAR="/project/arjunrajlab/refs/STAR/hg38"    # This file contains an index used by the STAR aligner. You need to change the index if you're not using the hg38 reference genome.
gtfFile="/project/arjunrajlab/refs/hg38/hg38.gtf"      # This reference file contains annotation information for hg38 genes. Change it to a different file for a different reference genome.
#######################

## Update these variables below to your project name, experiment name, number of samples,
#  code home directory (where your "rajlabseqtools/Utilities" folder is. if it's in your
#  home directory (e.g. /home/esanford), you can leave the "~" symbol)
PROJECT="HistoryDependence"
EXPERIMENT="HD3_RNA-Seq"
RAWDATA_DIRECTORY="/home/esanford/data/HD3_RNA-Seq/data_from_illumina"
N_SAMPLES=11
PAIRED_OR_SINGLE_END_FRAGMENTS="single"  # this variable must be "single" or "paired". change to "paired" if your reads... are paired.
codeHomeDir=~                            # "~" is a shortcut for your home directory. alternatively you can use /home/<YOUR_PMACS_USERNAME>