2021 Catch-up
Environment setup
Directories and symlinks
Directories and links needed in your home directory.
cd
ln -s -f $SCRATCH scratch
ln -s -f $WORK2 work2
ln -s -f /work2/projects/BioITeam
ln -s -f /work2/projects/BioITeam/projects/courses/Core_NGS_Tools CoreNGS
mkdir -p ~/local/bin
cd ~/local/bin
ln -s -f /work2/projects/BioITeam/common/bin/launcher_creator.py
ln -s -f /work2/projects/BioITeam/common/bin/launcher_maker.py
.bashrc setup
If you already have a .bashrc set up, make a backup copy first. You can restore your original login script after class is over.
cd
cp .bashrc .bashrc.beforeNGSToolsCopy and configure the login profile for this class
cd
cp /work2/projects/BioITeam/projects/courses/Core_NGS_Tools/tacc/bashrc.corengs.stampede2 .bashrc
chmod 600 .bashrc
# or, using your symlink
cd
cp ~/CoreNGS/tacc/bashrc.corengs.stampede2 .bashrc
chmod 600 .bashrcSource it to make it active (if this doesn't work, log off then log back in):
Copy a pre-configured login script
source ~/.bashrcEnvironment variables
General
export ALLOCATION=UT-2015-05-18
export BIWORK=/work2/projects/BioITeam
export CORENGS=$BIWORK/projects/courses/Core_NGS_Tools
export PATH=.:$HOME/local/bin:$PATH
Turn on coloring by file type in the shell:
# For better colors using a dark background terminal, un-comment this line:
export LS_COLORS=$LS_COLORS:'di=1;33:fi=01:ln=01;36:'
# For better colors using a white background terminal:
export LS_COLORS=$LS_COLORS:'di=1;34:fi=01:ln=01;36:'
# May or may not be needed
export LS_OPTIONS='-N --color=auto -T 0TACC 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 120 -N 1 -n 68 -A UT-2015-05-18 --reservation=BIO_DATA_week_1You can tell you're in a idev session because the hostname command will return a compute node name (e.g. c401-041.stampede2.tacc.utexas.edu) instead of a login node name (e.g. login2.stampede2.tacc.utexas.edu).
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:
# Create a $SCRATCH area to work on data for this course,
# with a sub-direct[1ory for pre-processing raw fastq files
mkdir -p $SCRATCH/core_ngs/fastq_prep
# Make symbolic links to the original yeast data:
cd $SCRATCH/core_ngs/fastq_prep
ln -s -f $CORENGS/yeast_stuff/Sample_Yeast_L005_R1.cat.fastq.gz
ln -s -f $CORENGS/yeast_stuff/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 biocontainers # takes a while
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 biocontainers # takes a while
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 biocontainers # takes a while
module load samtools