Needed to assess the Hematodinium sp. transcriptomes that I’ve assembled to determine their “completeness” using BUSCO.
-
hemat_transcriptome_v1.6.fasta (4.5MB; from 20210308)
-
hemat_transcriptome_v1.7.fasta (1.9MB; from 20210308)
-
hemat_transcriptome_v2.1.fasta (65MB; from 20200605)
-
hemat_transcriptome_v3.1.fasta (65MB; from 20200605)
All of the above transcriptomes were assembled with different combinations of the crab RNAseq data we generated. Here’s a link to an overview of the various assemblies:
- hemat_transcriptome_comp (Google Sheet)
SBATCH script (GitHub):
#!/bin/bash
## Job Name
#SBATCH --job-name=cbai_busco_megan_transcriptomes
## Allocation Definition
#SBATCH --account=coenv
#SBATCH --partition=coenv
## Resources
## Nodes
#SBATCH --nodes=1
## Walltime (days-hours:minutes:seconds format)
#SBATCH --time=3-00:00:00
## Memory per node
#SBATCH --mem=120G
##turn on e-mail notification
#SBATCH --mail-type=ALL
#SBATCH --mail-user=samwhite@uw.edu
## Specify the working directory for this job
#SBATCH --chdir=/gscratch/scrubbed/samwhite/outputs/20200814_hemat_busco_transcriptomes_v1.6_v1.7_v2.1_v.3.1
###################################################################################
# These variables need to be set by user
## Save working directory
wd=$(pwd)
# Establish variables for more readable code
transcriptomes_dir=/gscratch/srlab/sam/data/Hematodinium/transcriptomes
# Array of the various comparisons to evaluate
# Each condition in each comparison should be separated by a "-"
transcriptomes_array=(
"${transcriptomes_dir}"/hemat_transcriptome_v1.6.fasta \
"${transcriptomes_dir}"/hemat_transcriptome_v1.7.fasta \
"${transcriptomes_dir}"/hemat_transcriptome_v2.1.fasta \
"${transcriptomes_dir}"/hemat_transcriptome_v3.1.fasta
)
## Input files and settings
busco_db=/gscratch/srlab/sam/data/databases/BUSCO/metazoa_odb9
augustus_species=fly
threads=28
# Programs array
declare -A programs_array
programs_array=(
[busco]="/gscratch/srlab/programs/busco-v3/scripts/run_BUSCO.py"
)
## Set program paths
augustus_bin=/gscratch/srlab/programs/Augustus-3.3.2/bin
augustus_orig_config_dir=/gscratch/srlab/programs/Augustus-3.3.2/config
augustus_scripts=/gscratch/srlab/programs/Augustus-3.3.2/scripts
blast_dir=/gscratch/srlab/programs/ncbi-blast-2.8.1+/bin/
hmm_dir=/gscratch/srlab/programs/hmmer-3.2.1/src/
# Export Augustus variable
export PATH="${augustus_bin}:$PATH"
export PATH="${augustus_scripts}:$PATH"
## BUSCO configs
busco_config_default=/gscratch/srlab/programs/busco-v3/config/config.ini.default
busco_config_ini=${wd}/config.ini
# Export BUSCO config file location
export BUSCO_CONFIG_FILE="${busco_config_ini}"
# Copy BUSCO config file
cp ${busco_config_default} "${busco_config_ini}"
# Edit BUSCO config file
## Set paths to various programs
### The use of the % symbol sets the delimiter sed uses for arguments.
### Normally, the delimiter that most examples use is a slash "/".
### But, we need to expand the variables into a full path with slashes, which screws up sed.
### Thus, the use of % symbol instead (it could be any character that is NOT present in the expanded variable; doesn't have to be "%").
sed -i "/^;cpu/ s/1/${threads}/" "${busco_config_ini}"
sed -i "/^tblastn_path/ s%tblastn_path = /usr/bin/%path = ${blast_dir}%" "${busco_config_ini}"
sed -i "/^makeblastdb_path/ s%makeblastdb_path = /usr/bin/%path = ${blast_dir}%" "${busco_config_ini}"
sed -i "/^augustus_path/ s%augustus_path = /home/osboxes/BUSCOVM/augustus/augustus-3.2.2/bin/%path = ${augustus_bin}%" "${busco_config_ini}"
sed -i "/^etraining_path/ s%etraining_path = /home/osboxes/BUSCOVM/augustus/augustus-3.2.2/bin/%path = ${augustus_bin}%" "${busco_config_ini}"
sed -i "/^gff2gbSmallDNA_path/ s%gff2gbSmallDNA_path = /home/osboxes/BUSCOVM/augustus/augustus-3.2.2/scripts/%path = ${augustus_scripts}%" "${busco_config_ini}"
sed -i "/^new_species_path/ s%new_species_path = /home/osboxes/BUSCOVM/augustus/augustus-3.2.2/scripts/%path = ${augustus_scripts}%" "${busco_config_ini}"
sed -i "/^optimize_augustus_path/ s%optimize_augustus_path = /home/osboxes/BUSCOVM/augustus/augustus-3.2.2/scripts/%path = ${augustus_scripts}%" "${busco_config_ini}"
sed -i "/^hmmsearch_path/ s%hmmsearch_path = /home/osboxes/BUSCOVM/hmmer/hmmer-3.1b2-linux-intel-ia32/binaries/%path = ${hmm_dir}%" "${busco_config_ini}"
###################################################################################
# Load Python Mox module for Python module availability
module load intel-python3_2017
# Load Open MPI module for parallel, multi-node processing
module load icc_19-ompi_3.1.2
# SegFault fix?
export THREADS_DAEMON_MODEL=1
for transcriptome in "${!transcriptomes_array[@]}"
do
# Remove path from transcriptome using parameter substitution
transcriptome_name="${transcriptomes_array[$transcriptome]##*/}"
## Augustus config directories
augustus_dir=${wd}/${transcriptome_name}_augustus
augustus_config_dir=${augustus_dir}/config
export AUGUSTUS_CONFIG_PATH="${augustus_config_dir}"
# Make Augustus directory if it doesn't exist
if [ ! -d "${augustus_dir}" ]; then
mkdir --parents "${augustus_dir}"
fi
# Copy Augustus config directory
cp --preserve -r ${augustus_orig_config_dir} "${augustus_dir}"
# Run BUSCO/Augustus training
${programs_array[busco]} \
--in ${transcriptomes_array[$transcriptome]} \
--out ${transcriptome_name} \
--lineage_path ${busco_db} \
--mode transcriptome \
--cpu ${threads} \
--long \
--species ${augustus_species} \
--tarzip \
--augustus_parameters='--progress=true'
# Capture FastA checksums for verification
cho ""
echo "Generating checksum for ${transcriptome_name}"
md5sum "${transcriptomes_array[$transcriptome]}" > "${transcriptome_name}".checksum.md5
echo "Finished generating checksum for ${transcriptome_name}"
echo ""
done
# Document programs in PATH (primarily for program version ID)
{
date
echo ""
echo "System PATH for $SLURM_JOB_ID"
echo ""
printf "%0.s-" {1..10}
echo "${PATH}" | tr : \\n
} >> system_path.log
# Capture program options
for program in "${!programs_array[@]}"
do
{
echo "Program options for ${program}: "
echo ""
${programs_array[$program]} --help
echo ""
echo ""
echo "----------------------------------------------"
echo ""
echo ""
} &>> program_options.log || true
done
RESULTS
Just under 7mins to assess the four transcriptomes:
Output folder:
All data below has been added to a transcriptome comparison spreadsheet:
- hemat_transcriptome_comp (Google Sheet)
hemat_transcriptome_v1.6.fasta BUSCO Short Summary
# BUSCO version is: 3.0.2
# The lineage dataset is: metazoa_odb9 (Creation date: 2016-02-13, number of species: 65, number of BUSCOs: 978)
# To reproduce this run: python /gscratch/srlab/programs/busco-v3/scripts/run_BUSCO.py -i /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v1.6.fasta -o hemat_transcriptome_v1.6.fasta -l /gscratch/srlab/sam/data/databases/BUSCO/metazoa_odb9/ -m transcriptome -c 28 --long -z
#
# Summarized benchmarking in BUSCO notation for file /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v1.6.fasta
# BUSCO was run in mode: transcriptome
C:26.5%[S:20.7%,D:5.8%],F:11.2%,M:62.3%,n:978
259 Complete BUSCOs (C)
202 Complete and single-copy BUSCOs (S)
57 Complete and duplicated BUSCOs (D)
110 Fragmented BUSCOs (F)
609 Missing BUSCOs (M)
978 Total BUSCO groups searched
hemat_transcriptome_v1.7.fasta BUSCO Short Summary
# BUSCO version is: 3.0.2
# The lineage dataset is: metazoa_odb9 (Creation date: 2016-02-13, number of species: 65, number of BUSCOs: 978)
# To reproduce this run: python /gscratch/srlab/programs/busco-v3/scripts/run_BUSCO.py -i /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v1.7.fasta -o hemat_transcriptome_v1.7.fasta -l /gscratch/srlab/sam/data/databases/BUSCO/metazoa_odb9/ -m transcriptome -c 28 --long -z
#
# Summarized benchmarking in BUSCO notation for file /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v1.7.fasta
# BUSCO was run in mode: transcriptome
C:15.0%[S:12.2%,D:2.8%],F:12.3%,M:72.7%,n:978
146 Complete BUSCOs (C)
119 Complete and single-copy BUSCOs (S)
27 Complete and duplicated BUSCOs (D)
120 Fragmented BUSCOs (F)
712 Missing BUSCOs (M)
978 Total BUSCO groups searched
hemat_transcriptome_v2.1.fasta BUSCO Short Summary
# BUSCO version is: 3.0.2
# The lineage dataset is: metazoa_odb9 (Creation date: 2016-02-13, number of species: 65, number of BUSCOs: 978)
# To reproduce this run: python /gscratch/srlab/programs/busco-v3/scripts/run_BUSCO.py -i /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v2.1.fasta -o hemat_transcriptome_v2.1.fasta -l /gscratch/srlab/sam/data/databases/BUSCO/metazoa_odb9/ -m transcriptome -c 28 --long -z
#
# Summarized benchmarking in BUSCO notation for file /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v2.1.fasta
# BUSCO was run in mode: transcriptome
C:33.7%[S:6.2%,D:27.5%],F:2.9%,M:63.4%,n:978
330 Complete BUSCOs (C)
61 Complete and single-copy BUSCOs (S)
269 Complete and duplicated BUSCOs (D)
28 Fragmented BUSCOs (F)
620 Missing BUSCOs (M)
978 Total BUSCO groups searched
hemat_transcriptome_v3.1.fasta BUSCO Short Summary
# BUSCO version is: 3.0.2
# The lineage dataset is: metazoa_odb9 (Creation date: 2016-02-13, number of species: 65, number of BUSCOs: 978)
# To reproduce this run: python /gscratch/srlab/programs/busco-v3/scripts/run_BUSCO.py -i /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v3.1.fasta -o hemat_transcriptome_v3.1.fasta -l /gscratch/srlab/sam/data/databases/BUSCO/metazoa_odb9/ -m transcriptome -c 28 --long -z
#
# Summarized benchmarking in BUSCO notation for file /gscratch/srlab/sam/data/Hematodinium/transcriptomes/hemat_transcriptome_v3.1.fasta
# BUSCO was run in mode: transcriptome
C:34.3%[S:6.3%,D:28.0%],F:3.2%,M:62.5%,n:978
336 Complete BUSCOs (C)
62 Complete and single-copy BUSCOs (S)
274 Complete and duplicated BUSCOs (D)
31 Fragmented BUSCOs (F)
611 Missing BUSCOs (M)
978 Total BUSCO groups searched