TRNL Sequencing Test Bioinformatics

salloc --account=microbiome -t 0-05:00

mkdir -p /gscratch/grandol1/TRNL_Test/rawdata

cd /gscratch/grandol1/TRNL_Test/rawdata

unpigz --to-stdout /project/microbiome/data_queue/seq/TRNL_Test/rawdata/TRNL_Test_S1_L001_R1_001.fastq | split -l 1000000 -d --suffix-length=3 --additional-suffix=.fastq - TRNL_Test_R1_ ;
unpigz --to-stdout /project/microbiome/data_queue/seq/TRNL_Test/rawdata/TRNL_Test_S1_L001_R2_001.fastq | split -l 1000000 -d --suffix-length=3 --additional-suffix=.fastq - TRNL_Test_R2_

//project/microbiome/data_queue/seq/TRNL_Test/rawdata/run_parse_count_onSplitInput.pl

cd /project/microbiome/data_queue/seq/TRNL_Test/rawdata

./run_splitFastq_fwd.sh

./run_splitFastq_rev.sh

./run_aggregate.sh

cd /project/microbiome/data_queue/seq/TRNL_Test/tfmergedreads

./run_slurm_mergereads.pl

Just analyzing trimmed R1s to avoid suspected merge bias because of 2 x 150 sequencing:

cd /project/microbiome/data/seq/gtl_tests/TRNL_Test/tfmergedreads/16S/TRNL1/trimmed

cp ./*R1.fq /project/microbiome/data_queue/seq/TRNL_Test/

cd /project/microbiome/data/seq/TRNL_Test/

sed -n '1~4s/^@/>/p;2~4p' ./*.fq > ./TrnlTest16S.fa

vsearch --derep_fulllength $s TrnlTest16S.fa \
        --strand plus \
        --output $s derep.fa \
        --sizeout \
        --uc $s.derep.uc \
        --relabel $s. \
        --fasta_width 0

vsearch --cluster_unoise derep.fa --centroids zotus_vsearch.fa --sizein --sizeout

Bioinformatics v2:

Reran 1st attempt commands starting with “./run_slurm_mergereads.pl“

Edited “215” in the below code chunk of trim_merge.pl to “115”

system("vsearch --fastx_filter $R1tmpA --fastq_trunclen 215 --fastqout $R1tmpB --threads 32");
system("vsearch --fastx_filter $R2tmpA --fastq_trunclen 215 --fastqout $R2tmpB --threads 32");
print "vsearch step1 complete\n";
if(-e $R1tmpB && -e $R1tmpB){ 
    system("vsearch --fastq_join $R1tmpB --reverse $R2tmpB --fastaout $joinedfile --threads 32");
    unlink($R1tmpA, $R2tmpA, $R1tmpB, $R2tmpB);
}