Initial commit
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#!/bin/bash
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#PBS -N compleasm_first
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#PBS -l nodes=1:ppn=TOTAL_THREADS # Replace with total available CPUs (e.g., 64)
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#PBS -l mem=384gb # Adjust based on ppn × 6GB
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#PBS -l walltime=24:00:00
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cd $PBS_O_WORKDIR
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source ~/.bashrc
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conda activate phylo
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mkdir -p logs
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mkdir -p 01_busco_results
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# Process FIRST genome only (downloads lineage database)
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first_genome=$(head -n 1 genome_list.txt)
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genome_name=$(basename ${first_genome} .fasta)
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echo "Processing first genome: ${genome_name} with $PBS_NUM_PPN threads..."
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echo "This will download the BUSCO lineage database for subsequent runs."
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compleasm run \
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-a ${first_genome} \
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-o 01_busco_results/${genome_name}_compleasm \
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-l LINEAGE \
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-t $PBS_NUM_PPN
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echo "First genome complete! Lineage database is now cached."
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echo "Submit the parallel job for remaining genomes: qsub run_compleasm_parallel.job"
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#!/bin/bash
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#PBS -N compleasm_parallel
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#PBS -t 2-NUM_GENOMES # Start from genome 2 (first genome already processed)
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#PBS -l nodes=1:ppn=THREADS_PER_JOB # e.g., 16 for 64-core system
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#PBS -l mem=96gb # Adjust based on ppn × 6GB
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#PBS -l walltime=48:00:00
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cd $PBS_O_WORKDIR
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source ~/.bashrc
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conda activate phylo
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mkdir -p 01_busco_results
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# Get genome for this array task
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genome=$(sed -n "${PBS_ARRAYID}p" genome_list.txt)
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genome_name=$(basename ${genome} .fasta)
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echo "Processing ${genome_name} with $PBS_NUM_PPN threads..."
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compleasm run \
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-a ${genome} \
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-o 01_busco_results/${genome_name}_compleasm \
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-l LINEAGE \
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-t $PBS_NUM_PPN
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#!/bin/bash
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#PBS -N iqtree_partition
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#PBS -l nodes=1:ppn=18
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#PBS -l mem=72gb
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#PBS -l walltime=72:00:00
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cd $PBS_O_WORKDIR/06_concatenation
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source ~/.bashrc
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conda activate phylo
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iqtree \
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-s FcC_supermatrix.fas \
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-spp partition_def.txt \
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-nt 18 \
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-safe \
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-pre partition_search \
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-m TESTMERGEONLY \
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-mset MODEL_SET \
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-msub nuclear \
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-rcluster 10 \
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-bb 1000 \
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-alrt 1000
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@@ -0,0 +1,26 @@
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#!/bin/bash
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#PBS -N iqtree_genes
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#PBS -t 1-NUM_LOCI
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#PBS -l nodes=1:ppn=1
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#PBS -l mem=4gb
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#PBS -l walltime=2:00:00
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cd $PBS_O_WORKDIR/trimmed_aa
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source ~/.bashrc
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conda activate phylo
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# Create list of alignments if not present
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if [ ! -f locus_alignments.txt ]; then
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ls *_trimmed.fas > locus_alignments.txt
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fi
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locus=$(sed -n "${PBS_ARRAYID}p" locus_alignments.txt)
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iqtree \
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-s ${locus} \
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-m MFP \
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-bb 1000 \
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-bnni \
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-czb \
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-pre $(basename ${locus} _trimmed.fas) \
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-nt 1
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