2020 Catch-up
Environment setup
Directories and symlinks
Directories and links needed in your home directory.
cd
ln -s -f $SCRATCH scratch
ln -s -f $WORK work
ln -s -f /work/projects/BioITeam
mkdir -p ~/local/bin
cd ~/local/bin
ln -s -f /work/projects/BioITeam/common/bin/launcher_maker.py
ln -s -f /work/projects/BioITeam/ls5/opt/cutadapt-1.10/bin/cutadapt
ln -s -f /work/projects/BioITeam/ls5/opt/multiqc-1.0/multiqc
ln -s -f /work/projects/BioITeam/ls5/opt/samstat-1.09/samstat.bashrc setup
If you already have a .bashrc set up, make a backup copy first. You can restore your original login script after class is over.
cd
cp .bashrc .bashrc.beforeNGSCopy and configure the login profile for this class
cd
cp /work/projects/BioITeam/projects/courses/Core_NGS_Tools/tacc/bashrc.corengs.ls5 .bashrc
chmod 600 .bashrcSource it to make it active (if this doesn't work, log off then log back in):
Copy a pre-configured login script
source ~/.bashrcEnvironment variables
General
export ALLOCATION=UT-2015-05-18
export BI=/corral-repl/utexas/BioITeam
export BIWORK=/work/projects/BioITeam
export CORENGS=$BIWORK/projects/courses/Core_NGS_Tools
export PATH=.:$HOME/local/bin:$PATH
# For cutadapt support:
export PYTHONPATH=$BIWORK/ls5/lib/python2.7/site-packages:$PYTHONPATH
# For MultiQC support:
export PYTHONPATH=$BIWORK/ls5/lib/python2.7/annab-packages:$PYTHONPATH
Turn on coloring by file type in the shell:
export LS_OPTIONS='-N --color=auto -T 0'
# For better colors using a white background terminal, un-comment this line:
export LS_COLORS=$LS_COLORS:'di=1;33:'
# For better colors using a white background terminal:
export LS_COLORS=$LS_COLORS:'di=1;34:'TACC intro
Commands files
Simple commands
mkdir -p $SCRATCH/core_ngs/slurm/simple
cd $SCRATCH/core_ngs/slurm/simple
cp $CORENGS/tacc/simple.cmds Wayness commands
mkdir -p $SCRATCH/core_ngs/slurm/wayness
cd $SCRATCH/core_ngs/slurm/wayness
cp $CORENGS/tacc/wayness.cmds .Start an idev session
To start a 3-hour idev (interactive development) session:
Start an idev session
idev -p normal -m 180 -N 1 -n 24 -A UT-2015-05-18 --reservation=CCBBYou can tell you're in a idev session because the hostname command will return a compute node name (e.g. nid00438) instead of a login node name (e.g. login5).
The n idev session will terminate when the requested time has expired, or you use the exit command.
Working with FASTQ
Yeast data
Working with some yeast ChIP-seq FASTQ data:
# Area for "original" sequencing data
mkdir -p $WORK/archive/original/2018_05.core_ngs
cd $WORK/archive/original/2018_05.core_ngs
wget http://web.corral.tacc.utexas.edu/BioITeam/yeast_stuff/Sample_Yeast_L005_R1.cat.fastq.gz
wget http://web.corral.tacc.utexas.edu/BioITeam/yeast_stuff/Sample_Yeast_L005_R2.cat.fastq.gz
# Create a $SCRATCH area for FASTQ prep and link the yeast data there
mkdir -p $SCRATCH/core_ngs/fastq_prep
cd $SCRATCH/core_ngs/fastq_prep
ln -s -f $WORK/archive/original/2018_05.core_ngs/Sample_Yeast_L005_R1.cat.fastq.gz
ln -s -f $WORK/archive/original/2018_05.core_ngs/Sample_Yeast_L005_R2.cat.fastq.gz
# Copy over a small FASTQ file
cd $SCRATCH/core_ngs/fastq_prep
cp $CORENGS/misc/small.fq .ATACseq data for MultiQC
Get some FastQC reports for MultiQC:
mkdir -p $SCRATCH/core_ngs/multiqc/fqc.atacseq
cd $SCRATCH/core_ngs/multiqc/fqc.atacseq
cp $CORENGS/multiqc/fqc.atacseq/*.html FASTQ files for cutadapt
For command-line cutadapt exploration:
cd $SCRATCH/core_ngs/fastq_prep
cp $CORENGS/human_stuff/Sample_H54_miRNA_L004_R1.cat.fastq.gz .
cp $CORENGS/human_stuff/Sample_H54_miRNA_L005_R1.cat.fastq.gz .
zcat Sample_H54_miRNA_L004_R1.cat.fastq.gz | head -2000 > miRNA_test.fqFor batch cutadapt processing:
mkdir -p $SCRATCH/core_ngs/cutadapt
cd $SCRATCH/core_ngs/cutadapt
cp $CORENGS/human_stuff/Sample_H54_miRNA_L004_R1.cat.fastq.gz .
cp $CORENGS/human_stuff/Sample_H54_miRNA_L005_R1.cat.fastq.gz .
cp $CORENGS/yeast_stuff/Yeast_RNAseq_L002_R1.fastq.gz .
cp $CORENGS/yeast_stuff/Yeast_RNAseq_L002_R2.fastq.gz .
cp $CORENGS/tacc/cuta.cmds .Alignment workflow
Alignment workflow setup
Starting files:
# FASTA (for building references)
mkdir -p $SCRATCH/core_ngs/references/fasta
cp $CORENGS/references/*.* $SCRATCH/core_ngs/references/fasta/
# FASTQ (to align)
mkdir -p $SCRATCH/core_ngs/alignment/fastq
cp $CORENGS/alignment/*fastq.gz $SCRATCH/core_ngs/alignment/fastq/
References
Get a copy of all references we build in the exercises (including FASTA):
mkdir -p $SCRATCH/core_ngs/references
rsync -ptlvrP $CORENGS/references/ $SCRATCH/core_ngs/references/
BWA PE alignment of yeast data
To jump into aligning PE yeast data with BWA
# Pre-built references
mkdir -p $SCRATCH/core_ngs/references
rsync -avrP $CORENGS/references/ $SCRATCH/core_ngs/references/
# FASTQ (to align)
mkdir -p $SCRATCH/core_ngs/alignment/fastq
cp $CORENGS/alignment/*fastq.gz $SCRATCH/core_ngs/alignment/fastq/
# Alignment directory
mkdir -p $SCRATCH/core_ngs/alignment/yeast_bwa
cd $SCRATCH/core_ngs/alignment/yeast_bwa
ln -s -f ../fastq
ln -s -f ../../references/bwa/sacCer3
module load bwa
module load samtoolssamtools manipulation of aligned yeast data
To jump into post-alignment manipulation of the yeast_pairedend.bam with samtools:
mkdir -p $SCRATCH/core_ngs/alignment/yeast_bwa
cd $SCRATCH/core_ngs/alignment/yeast_bwa
cp $CORENGS/catchup/yeast_bwa/yeast_pairedend.bam .
module load samtools
# If the sorted, indexed BAM is needed:
cp $CORENGS/catchup/yeast_bwa/yeast_pairedend.sort* .SAMTools and BEDTools
Setup for samtools
Setup for samtools exercises
mkdir -p $SCRATCH/core_ngs/samtools
cd $SCRATCH/core_ngs/samtools
cp $CORENGS/catchup/for_samtools/* .
module load samtools