--- author: Sam White toc-title: Contents toc-depth: 5 toc-location: left layout: post title: Taxonomic Assignments - C.bairdi 6129-403-26-Q7 NanoPore Reads Using DIAMOND BLASTx on Mox and MEGAN6 daa2rma on emu date: '2020-09-28 19:49' tags: - Chionoecetes bairdi - Tanner crab - mox - BLASTx - DIAMOND - nanopore - emu categories: - 2020 - Miscellaneous --- After noticing that the [initial MEGAN6 taxonomic assignments for our combined _C.bairdi_ NanoPore data from 20200917](https://robertslab.github.io/sams-notebook/posts/2020/2020-09-17-Taxonomic-Assignments---C.bairdi-NanoPore-Reads-Using-DIAMOND-BLASTx-on-Mox-and-MEGAN6-daa2rma-on-swoose/) revealed a high number of bases assigned to _E.canceri_ and _Aquifex sp._, I decided to explore the taxonomic breakdown of just the individual samples to see which of the samples was contributing to these taxonomic assignments most. Ran the _Hematodinium_-infected (6129_403_26_Q7) hemolymph NanoPore sequencing data through DIAMOND BLASTx (on Mox) and subsequent output conversion to the MEGAN6 RMA6 format (on swoose due to program Java X11 requirement which is not functional on Mox) to obtain taxonomic assignments. SBATCH script (GitHub): - [20200928_cbai_diamond_blastx_nanopore_6129_403_26_Q7.sh](https://github.com/RobertsLab/sams-notebook/blob/master/sbatch_scripts/20200928_cbai_diamond_blastx_nanopore_6129_403_26_Q7.sh) ```shell #!/bin/bash ## Job Name #SBATCH --job-name=cbai_blastx_DIAMOND_nanopore_6129_403_26_Q7 ## Allocation Definition #SBATCH --account=coenv #SBATCH --partition=coenv ## Resources ## Nodes #SBATCH --nodes=1 ## Walltime (days-hours:minutes:seconds format) #SBATCH --time=10-00:00:00 ## Memory per node #SBATCH --mem=200G ##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/20200928_cbai_diamond_blastx_nanopore_6129_403_26_Q7 # Script to run DIAMOND BLASTx on 6129_403_26 quality filtered (Q7) C.bairdi NanoPore reads # from 20200928 using the --long-reads option # for subsequent import into MEGAN6 to evaluate reads taxonomically. ################################################################################### # These variables need to be set by user # Input FastQ file fastq=/gscratch/srlab/sam/data/C_bairdi/DNAseq/20200928_cbai_nanopore_6129_403_26_quality-7.fastq # DIAMOND Output filename prefix prefix=20200928_cbai_nanopore_6129_403_26_Q7 # Set number of CPUs to use threads=28 # Program paths diamond=/gscratch/srlab/programs/diamond-2.0.4/diamond # DIAMOND NCBI nr database with taxonomy dumps dmnd_db=/gscratch/srlab/blastdbs/ncbi-nr-20190925/nr.dmnd ################################################################################### # Exit script if any command fails set -e # Load Python Mox module for Python module availability module load intel-python3_2017 # SegFault fix? export THREADS_DAEMON_MODEL=1 # Inititalize arrays programs_array=() # Programs array programs_array=("${diamond}") md5sum "${fastq}" > fastq_checksums.md5 # Run DIAMOND with blastx # Output format 6 produces a standard BLAST tab-delimited file # Run DIAMOND with blastx # Output format 100 produces a DAA binary file for use with MEGAN ${diamond} blastx \ --long-reads \ --db ${dmnd_db} \ --query "${fastq}" \ --out "${prefix}".blastx.daa \ --outfmt 100 \ --top 5 \ --block-size 8.0 \ --index-chunks 1 \ --threads ${threads} # Capture program options for program in "${!programs_array[@]}" do { echo "Program options for ${programs_array[program]}: " echo "" ${programs_array[program]} help echo "" echo "" echo "----------------------------------------------" echo "" echo "" } &>> program_options.log || true 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 ``` Bash script (GitHub) for `daa2rma` on Emu: - [20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma.sh](https://github.com/RobertsLab/sams-notebook/blob/master/bash_scripts/20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma.sh) ```shell #!/bin/bash # Script to run MEGAN6 daa2rma on DIAMOND DAA files from # 20200928_cbai_diamond_blastx_nanopore_6129_403_26_Q7. # Utilizes the --longReads option # Requires MEGAN mapping file from: # http://ab.inf.uni-tuebingen.de/data/software/megan6/download # MEGAN mapping file megan_map=/home/sam/data/databases/MEGAN6/megan-map-Jul2020-2.db # Programs array declare -A programs_array programs_array=( [daa2rma]="/home/shared/megan_6.19.9/tools/daa2rma" ) threads=16 ######################################################################### # Exit script if any command fails set -e ## Run daa2rma # Capture start "time" # Uses builtin bash variable called ${SECONDS} start=${SECONDS} for daa in *.daa do start_loop=${SECONDS} sample_name=$(basename --suffix ".blastx.daa" "${daa}") echo "Now processing ${sample_name}.daa2rma.rma6" echo "" # Run daa2rma with long reads option ${programs_array[daa2rma]} \ --in "${daa}" \ --longReads \ --mapDB ${megan_map} \ --out "${sample_name}".daa2rma.rma6 \ --threads ${threads} \ 2>&1 | tee --append daa2rma_log.txt end_loop=${SECONDS} loop_runtime=$((end_loop-start_loop)) echo "Finished processing ${sample_name}.daa2rma.rma6 in ${loop_runtime} seconds." echo "" done # Caputure end "time" end=${SECONDS} runtime=$((end-start)) # Print daa2rma runtime, in seconds { echo "" echo "---------------------" echo "" echo "Total runtime was: ${runtime} seconds" } >> daa2rma_log.txt # Capture program options for program in "${!programs_array[@]}" do { echo "Program options for ${program}: " echo "" ${programs_array[$program]} --help echo "" echo "" echo "----------------------------------------------" echo "" echo "" } &>> program_options.log || true done # Document programs in PATH { date echo "" echo "System PATH:" echo "" printf "%0.s-" {1..10} echo "${PATH}" | tr : \\n } >> system_path.log ``` --- # RESULTS Pretty quick, a little over 31mins: ![DIAMOND BLASTx and MEGAN daa2rma conversion for 6129-403-26-Q7 runtime](https://github.com/RobertsLab/sams-notebook/blob/master/images/screencaps/20200928_cbai_diamond_blastx_nanopore_6129_403_26_Q7_runtime.png?raw=true) DIAMOND BLASTx Output folder: - [20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/](https://gannet.fish.washington.edu/Atumefaciens/20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/) - DIAMOND BLASTx DAA file: - [20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/20200928_cbai_nanopore_6129-403-26_Q7.blastx.daa](https://gannet.fish.washington.edu/Atumefaciens/20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/20200928_cbai_nanopore_6129-403-26_Q7.blastx.daa) (265MB) - RMA6 file: - [20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/20200928_cbai_nanopore_6129-403-26_Q7.daa2rma.rma6](https://gannet.fish.washington.edu/Atumefaciens/20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma/20200928_cbai_nanopore_6129-403-26_Q7.daa2rma.rma6) (256MB) ##### Taxonomic tree ![6129-403-26-Q7 MEGAN6 taxonomic assignments](https://github.com/RobertsLab/sams-notebook/blob/master/images/screencaps/20200928_cbai_nanopore_6129-403-26-Q7_diamond_blastx_daa2rma_megan-taxonomic-tree.png?raw=true) Alrighty, we see both _Alveolata_/_Hematodinium sp._, E.canceri_ _Aquifex sp._ taxonomic assignments (and, of course _Arthropoda_). A large number of bases (~34Mbp) are assigned to _Arthropoda_. _Alveolata_ only has ~400kbp assigned, while _E.canceri_ has ~17Mbp (!) and _Aquifex sp._ has ~6Mbp! Very surprising. [The other sample is here.](https://robertslab.github.io/sams-notebook/posts/2020/2020-09-28-Taxonomic-Assignments---C.bairdi-20102558-2729-Q7-NanoPore-Reads-Using-DIAMOND-BLASTx-on-Mox-and-MEGAN6-daa2rma-on-emu/) [Next, I'll run a comparison of the two sets of sequencing read taxonomic assignments for an easier overview.](https://robertslab.github.io/sams-notebook/posts/2020/2020-10-02-Comparison---C.bairdi-20102558-2729-vs.-6129-403-26-NanoPore-Taxonomic-Assignments-Using-MEGAN6/)