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16S_pipeline.V8.sh
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16S_pipeline.V8.sh
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#/bin/sh -S
#########
#Please address any bugs to Cheng.
#Date 2017.12.19
#########
echo $(readlink -f $1)
mapping_file=$(readlink -f $1)
depth=$2
min_freq=$3
category_set=${4//,/ }
category_report=($category_set)
reference_trained=$(readlink -f $5)
close_reference_trained=$(readlink -f $6)
manifest_file=$(readlink -f $7)
not_rda=$8
echo "Check wheather your categories are the following:"
for i in $category_set;do echo $i;done
declare -A tax_aa
tax_aa=([k]=Kingdom [p]=Phylum [c]=Class [o]=Order [f]=Family [g]=Genus [s]=Species)
tax_levels["1"]="Kingdom"
tax_levels["2"]="Phylum"
tax_levels["3"]="Class"
tax_levels["4"]="Order"
tax_levels["5"]="Family"
tax_levels["6"]="Genus"
tax_levels["7"]="Species"
#tax_levels1["k"]="Kingdom"
#tax_levels1["p"]="Phylum"
#tax_levels1["c"]="Class"
#tax_levels1["o"]="Order"
#tax_levels1["f"]="Family"
#tax_levels1["g"]="Genus"
#tax_levels1["s"]="Species"
if [ -z "$8" ]; then
echo "##########
Please prepare the directory structure before starting the program like below:
raw/fastq_files ...
mapping_file
manifest_file
\n\n"
echo "Please provide following input parameters
1) Path of the mapping file. (Accept both .csv or txt format.)
2) Depth of the for subsampleing. (Suggested value: 4000)
3) Mininum frequence for OTU to be selected. (Suggested value: 1000)
4) The name of categories in the mapping file seprated by commas.
5) Path of the classifier for alignment.
6) Path of the reference sequences for close reference alignment.
7) Path of the manifest file.
8) specify numeric variables excluded from rda seprated by commas,use 'none' if all numeric variables is expected
Sample Usage:
bash ~/github/Bayegy/16S_pipeline.V8.sh ../data/sample-metadata.tsv 20000 1000 Group1,Group2,Group3 ~/database_16S/338-806/gg_13_8_99_338_806_classifier.qza ~/database_16S/338-806/gg_13_5_97_338_806_ref_seqs.qza ../data/manifest.txt none
"
exit 0
else
echo "################
Running: sh $0 $1 $2 $3 $4 $5 $6 $7 $8"
fi
check_file() {
echo "Checking file for $1 ..."
file_name=$1
if [ -f $file_name ]; then
echo "File $file_name exists"
else
echo "File $file_name does not exist"
exit
fi
}
function assign_taxa() {
loop_id=$1
if [ $loop_id == 1]; then
echo "Kingdom"
elif [ $loop_id == 2]; then
echo "Phylum"
elif [ $loop_id == 3]; then
echo "Class"
elif [ $loop_id == 4]; then
echo "Order"
elif [ $loop_id == 5]; then
echo "Family"
elif [ $loop_id == 6]; then
echo "Genus"
elif [ $loop_id == 7]; then
echo "Species"
fi
}
#for f in 1 2 3 4 5 6 7;
# do echo $f;
# tax=$(assign_taxa ${f});
# echo $tax;
#done;
MAIN() {
##Activate Qiime2 Version
echo "##############################################################\n#Initiate directory name and set up the directory structure"
SCRIPTPATH="$( cd "$(dirname "$0")" ; pwd -P )"
#echo "##############################################################\n#Demultiplexing the single-end sequence file"
#qiime demux emp-single --i-seqs emp-single-end-sequences.qza --m-barcodes-file $mapping_file --m-barcodes-column BarcodeSequence --o-per-sample-sequences demux.qza
#qiime demux summarize --i-data demux.qza --o-visualization demux.qzv
#echo "##############################################################\n#Demultiplexing the paired-end sequence file"
#qiime demux emp-paired --i-seqs emp-paired-end-sequences.qza --m-barcodes-file $mapping_file --m-barcodes-column BarcodeSequence --o-per-sample-sequences demux.qza
#qiime demux summarize --i-data demux.qza --o-visualization demux.qzv
source activate qiime2-2018.8
<<com1
echo "##############################################################\n#Set up the directory structure and prepare the raw fastq sequences."
#check_file $manifest_file
#qiime tools import --type 'SampleData[SequencesWithQuality]' --input-path $manifest_file --output-path demux.qza --source-format SingleEndFastqManifestPhred64
#single-end
#qiime demux emp-single --i-seqs emp-single-end-sequences.qza --m-barcodes-file $mapping_file --m-barcodes-column BarcodeSequence --o-per-sample-sequences demux.qza --p-rev-comp-mapping-barcodes
#qiime demux emp-single --i-seqs ../database/emp-single-end-sequences.qza --m-barcodes-file $mapping_file --m-barcodes-column BarcodeSequence --o-per-sample-sequences demux.qza
#qiime tools import --type 'SampleData[SequencesWithQuality]' --input-path $manifest_file --output-path demux.qza --source-format SingleEndFastqManifestPhred33
#paired-end
qiime tools import --type 'SampleData[PairedEndSequencesWithQuality]' --input-path $manifest_file --output-path demux.qza --input-format PairedEndFastqManifestPhred33
qiime demux summarize --i-data demux.qza --o-visualization demux.qzv
echo "##############################################################\n#Use DADA2 for quality control and feature table construction"
#single-end
#qiime dada2 denoise-single --i-demultiplexed-seqs demux.qza --p-trim-left 10 --p-trunc-len 265 --o-representative-sequences rep-seqs-dada2.qza --o-table table-dada2.qza --p-n-threads 0 --o-denoising-stats stats-dada2.qza
#qiime dada2 denoise-single --i-demultiplexed-seqs demux.qza --p-trim-left 0 --p-trunc-len 120 --o-representative-sequences rep-seqs-dada2.qza --o-table table-dada2.qza --p-n-threads 0 --o-denoising-stats stats-dada2.qza --verbose
#paired-end
#qiime dada2 denoise-paired --i-demultiplexed-seqs demux.qza --p-trunc-len-f 210 --p-trunc-len-r 210 --p-trim-left-f 24 --p-trim-left-r 25 --o-representative-sequences rep-seqs-dada2.qza --o-table table-dada2.qza --p-n-threads 0 --o-denoising-stats stats-dada2.qza
qiime dada2 denoise-paired --i-demultiplexed-seqs demux.qza --p-trunc-len-f 290 --p-trunc-len-r 226 --p-trim-left-f 17 --p-trim-left-r 19 --o-representative-sequences rep-seqs-dada2.qza --o-table table-dada2.qza --p-n-threads 0 --o-denoising-stats stats-dada2.qza --verbose
#qiime dada2 denoise-paired --i-demultiplexed-seqs demux.qza --p-trunc-len-f 0 --p-trunc-len-r 0 --o-representative-sequences rep-seqs-dada2.qza --o-table table-dada2.qza --p-n-threads 0 --o-denoising-stats stats-dada2.qza
qiime metadata tabulate --m-input-file stats-dada2.qza --o-visualization stats-dada2.qzv
mv rep-seqs-dada2.qza rep-seqs.withCandM.qza
mv table-dada2.qza table.withCandM.qza
echo "##############################################################\n#Filter out Choloroplast and Mitochondira"
check_file $reference_trained
qiime feature-classifier classify-sklearn --i-classifier $reference_trained --i-reads rep-seqs.withCandM.qza --o-classification taxonomy.withCandM.qza
qiime metadata tabulate --m-input-file taxonomy.withCandM.qza --o-visualization taxonomy.withCandM.qzv
qiime taxa filter-table --i-table table.withCandM.qza --i-taxonomy taxonomy.withCandM.qza --p-exclude mitochondria,chloroplast,Archaea,Unassigned --o-filtered-table table-no-mitochondria-no-chloroplast.qza
mv table-no-mitochondria-no-chloroplast.qza table.qza
qiime taxa filter-seqs --i-sequences rep-seqs.withCandM.qza --i-taxonomy taxonomy.withCandM.qza --p-exclude mitochondria,chloroplast,Archaea,Unassigned --o-filtered-sequences rep-seqs-no-mitochondria-no-chloroplast.qza
mv rep-seqs-no-mitochondria-no-chloroplast.qza rep-seqs.qza
echo "##############################################################\n#Classify the taxonomy"
qiime feature-classifier classify-sklearn --i-classifier $reference_trained --i-reads rep-seqs.qza --o-classification taxonomy.qza
qiime metadata tabulate --m-input-file taxonomy.qza --o-visualization taxonomy.qzv
echo "##############################################################\n#Generate tree"
qiime alignment mafft --i-sequences rep-seqs.qza --o-alignment aligned-rep-seqs.qza
qiime alignment mask --i-alignment aligned-rep-seqs.qza --o-masked-alignment masked-aligned-rep-seqs.qza
qiime phylogeny fasttree --i-alignment masked-aligned-rep-seqs.qza --o-tree unrooted-tree.qza
qiime phylogeny midpoint-root --i-tree unrooted-tree.qza --o-rooted-tree rooted-tree.qza
com1
echo "##############################################################\n#Visulize of the table without Choloroplast and Mitochondira"
qiime feature-table summarize --i-table table.qza --o-visualization table.qzv --m-sample-metadata-file $mapping_file
qiime feature-table tabulate-seqs --i-data rep-seqs.qza --o-visualization rep-seqs.qzv
qiime taxa barplot --i-table table.qza --i-taxonomy taxonomy.qza --m-metadata-file $mapping_file --o-visualization taxa-bar-plots.qzv
echo "##############################################################\n#Core alpha and beta diversity analysis"
qiime diversity core-metrics-phylogenetic --i-phylogeny rooted-tree.qza --i-table table.qza --p-sampling-depth $depth --m-metadata-file $mapping_file --output-dir core-metrics-results
qiime diversity alpha-group-significance --i-alpha-diversity core-metrics-results/faith_pd_vector.qza --m-metadata-file $mapping_file --o-visualization core-metrics-results/faith-pd-group-significance.qzv
qiime diversity alpha-group-significance --i-alpha-diversity core-metrics-results/evenness_vector.qza --m-metadata-file $mapping_file --o-visualization core-metrics-results/evenness-group-significance.qzv
qiime diversity alpha-group-significance --i-alpha-diversity core-metrics-results/shannon_vector.qza --m-metadata-file $mapping_file --o-visualization core-metrics-results/shannon-group-significance.qzv
qiime diversity alpha-group-significance --i-alpha-diversity core-metrics-results/observed_otus_vector.qza --m-metadata-file $mapping_file --o-visualization core-metrics-results/observed_otus-group-significance.qzv
for category_1 in $category_set;
do echo $category_1;
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/unweighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_1 --o-visualization 'core-metrics-results/unweighted_unifrac-permanova-'$category_1'-significance.qzv' --p-pairwise;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/unweighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_2 --o-visualization 'core-metrics-results/unweighted_unifrac-permanova-'$category_2'-significance.qzv' --p-pairwise
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/weighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_1 --o-visualization 'core-metrics-results/weighted_unifrac-permanova-'$category_1'-significance.qzv' --p-pairwise;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/weighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_2 --o-visualization 'core-metrics-results/weighted_unifrac-permanova-'$category_2'-significance.qzv' --p-pairwise
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/bray_curtis_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_1 --o-visualization 'core-metrics-results/bray_curtis-permanova-'$category_1'-significance.qzv' --p-pairwise;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/bray_curtis_distance_matrix.qza --m-metadata-file $mapping_file --p-method permanova --m-metadata-column $category_2 --o-visualization 'core-metrics-results/bray_curtis-permanova-'$category_2'-significance.qzv' --p-pairwise
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/unweighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_1 --o-visualization 'core-metrics-results/unweighted_unifrac-anosim-'$category_1'-significance.qzv' --p-pairwise;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/unweighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_2 --o-visualization 'core-metrics-results/unweighted_unifrac-anosim-'$category_2'-significance.qzv' --p-pairwise
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/weighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_1 --o-visualization 'core-metrics-results/weighted_unifrac-anosim-'$category_1'-significance.qzv' --p-pairwise;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/weighted_unifrac_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_2 --o-visualization 'core-metrics-results/weighted_unifrac-anosim-'$category_2'-significance.qzv' --p-pairwise
qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/bray_curtis_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_1 --o-visualization 'core-metrics-results/bray_curtis-anosim-'$category_1'-significance.qzv' --p-pairwise;
done;
#qiime diversity beta-group-significance --i-distance-matrix core-metrics-results/bray_curtis_distance_matrix.qza --m-metadata-file $mapping_file --p-method anosim --m-metadata-column $category_2 --o-visualization 'core-metrics-results/bray_curtis-anosim-'$category_2'-significance.qzv' --p-pairwise
qiime diversity alpha-rarefaction --i-table table.qza --i-phylogeny rooted-tree.qza --p-max-depth $depth --m-metadata-file $mapping_file --o-visualization alpha-rarefaction.qzv --p-steps 50
##These following two commands work only for column with numeric values:
##qiime emperor plot --i-pcoa core-metrics-results/unweighted_unifrac_pcoa_results.qza --m-metadata-file $mapping_file --p-custom-axis $category_2 --o-visualization 'core-metrics-results/unweighted_unifrac-emperor-'$category_2'.qzv'
##qiime emperor plot --i-pcoa core-metrics-results/bray_curtis_pcoa_results.qza --m-metadata-file $mapping_file --p-custom-axis $category_2 --o-visualization 'core-metrics-results/bray-curtis-emperor-'$category_2'.qzv'
echo "##############################################################\n#alpha dviersity summary"
mkdir alpha
qiime diversity alpha --i-table table.qza --p-metric chao1 --output-dir alpha/chao1
qiime diversity alpha --i-table table.qza --p-metric shannon --output-dir alpha/shannon
qiime diversity alpha --i-table table.qza --p-metric observed_otus --output-dir alpha/observed_otus
qiime diversity alpha-phylogenetic --i-table table.qza --i-phylogeny rooted-tree.qza --p-metric faith_pd --output-dir alpha/faith_pd
qiime tools export --input-path alpha/chao1/alpha_diversity.qza --output-path alpha/chao1/
qiime tools export --input-path alpha/shannon/alpha_diversity.qza --output-path alpha/shannon/
qiime tools export --input-path alpha/observed_otus/alpha_diversity.qza --output-path alpha/observed_otus/
qiime tools export --input-path alpha/faith_pd/alpha_diversity.qza --output-path alpha/faith_pd/
paste alpha/observed_otus/alpha-diversity.tsv alpha/chao1/alpha-diversity.tsv alpha/shannon/alpha-diversity.tsv alpha/faith_pd/alpha-diversity.tsv | awk -F'\t' 'BEGIN{OFS="\t"}{print $1, $2, $4, $6, $8}' > alpha/alpha-summary.tsv
echo "##############################################################\n#Export necessary files for future analysis"
for f in rep-seqs.qza table.qza taxonomy.qza ; do echo $f; qiime tools export --input-path $f --output-path exported; done
for f in alpha-rarefaction.qzv table.qzv taxa-bar-plots.qzv; do echo $f; qiime tools export --input-path $f --output-path exported_qzv; done
qiime tools export --input-path rooted-tree.qza --output-path exported/
mv exported/tree.nwk exported/tree.rooted.nwk
qiime tools export --input-path unrooted-tree.qza --output-path exported/
mv exported/tree.nwk exported/tree.unrooted.nwk
biom add-metadata -i exported/feature-table.biom -o exported/feature-table.taxonomy.biom --observation-metadata-fp exported/taxonomy.tsv --observation-header OTUID,taxonomy,confidence
biom convert -i exported/feature-table.taxonomy.biom -o exported/feature-table.taxonomy.txt --to-tsv --header-key taxonomy
biom convert -i exported/feature-table.taxonomy.biom -o exported/feature-table.txt --to-tsv
sed 's/taxonomy/Consensus Lineage/' < exported/feature-table.taxonomy.txt | sed 's/ConsensusLineage/Consensus Lineage/' > exported/feature-table.ConsensusLineage.txt
echo "##############################################################\n#Generate heatmaps for top OTUs with different levels with minimum frequence reads supported"
mkdir exported/collapsed
mkdir exported/${min_freq}
for n in 2 3 4 5 6 7;
do echo $n;
qiime taxa collapse --i-table table.qza --i-taxonomy taxonomy.qza --p-level $n --o-collapsed-table exported/collapsed/collapsed-${tax_levels[${n}]}.qza;
qiime feature-table summarize --i-table exported/collapsed/collapsed-${tax_levels[${n}]}.qza --o-visualization exported/collapsed/collapsed-${tax_levels[${n}]}.qzv '--m-sample-metadata-file' $mapping_file;
qiime feature-table filter-features --i-table exported/collapsed/collapsed-${tax_levels[${n}]}.qza --p-min-frequency $min_freq --o-filtered-table exported/${min_freq}/table-${tax_levels[${n}]}.${min_freq}.qza;
for category_1 in $category_set;do echo $category_1;qiime feature-table heatmap --i-table exported/${min_freq}/table-${tax_levels[${n}]}.${min_freq}.qza --m-metadata-file $mapping_file --m-metadata-column $category_1 --o-visualization exported/${min_freq}/${category_1}-table-${tax_levels[${n}]}.${min_freq}.qzv;done;
done;
<<com2
source deactivate
source activate qm2
echo "##############################################################\n#Generate the figure for the percentage of annotated level"
perl ${SCRIPTPATH}/stat_otu_tab.pl -unif min exported/feature-table.taxonomy.txt -prefix exported/Relative/otu_table --even exported/Relative/otu_table.even.txt -spestat exported/Relative/classified_stat_relative.xls
perl ${SCRIPTPATH}/bar_diagram.pl -table exported/Relative/classified_stat_relative.xls -style 1 -x_title "Sample Name" -y_title "Sequence Number Percent" -right -textup -rotate='-45' --y_mun 1,7 > exported/Relative/Classified_stat_relative.svg
for key in ${!tax_aa[*]};do mv exported/Relative/otu_table.${key}.relative.mat exported/Relative/otu_table.${tax_aa[$key]}.relative.txt;done;
#mv exported/Relative/otu_table.p.relative.mat exported/Relative/otu_table.Phylum.relative.txt
#mv exported/Relative/otu_table.c.relative.mat exported/Relative/otu_table.Class.relative.txt
#mv exported/Relative/otu_table.o.relative.mat exported/Relative/otu_table.Order.relative.txt
#mv exported/Relative/otu_table.f.relative.mat exported/Relative/otu_table.Family.relative.txt
#mv exported/Relative/otu_table.g.relative.mat exported/Relative/otu_table.Genus.relative.txt
#mv exported/Relative/otu_table.s.relative.mat exported/Relative/otu_table.Species.relative.txt
for n7 in "Phylum" "Class" "Order" "Family" "Species";
do echo $n7;
#echo "mv exported/Relative/otu_table.${n7}.relative.mat exported/Relative/otu_table.${tax_levels[${n7}]}.relative.txt"
#mv exported/Relative/otu_table.${n7}.relative.mat exported/Relative/otu_table.${tax_levels[${n7}]}.relative.txt
#echo ${tax_levels[$n7]}
#echo ${tax_levels[${n7}]}
perl -lane '$,="\t";pop(@F);print(@F)' exported/Relative/otu_table.${n7}.relative.txt > exported/Relative/otu_table.${n7}.relative.lastcolumn.txt;
perl ${SCRIPTPATH}/get_table_head2.pl exported/Relative/otu_table.${n7}.relative.lastcolumn.txt 35 -trantab > exported/Relative/otu_table.${n7}.relative.lastcolumn.trans;
perl ${SCRIPTPATH}/bar_diagram.pl -table exported/Relative/otu_table.${n7}.relative.lastcolumn.trans -style 1 -x_title "Sample Name" -y_title "Sequence Number Percent" -right -textup -rotate='-45' --y_mun 1,1 > exported/Relative/otu_table.${n7}.relative.svg;
done;
for svg_file in exported/Relative/*svg; do echo $svg_file; n=$(basename "$svg_file" .svg); echo $n; rsvg-convert -h 3200 $svg_file > exported/Relative/${n}.png; done
source deactivate
source activate qiime2-2018.8
echo "ANCOM analaysis for differential OTU"
mkdir exported/ANCOM
for n2 in 2 3 4 5 6 7;
do echo $n2;
qiime composition add-pseudocount --i-table exported/collapsed/collapsed-${tax_levels[${n2}]}.qza --o-composition-table exported/ANCOM/composition.${tax_levels[${n2}]}.qza;
for category_1 in $category_set;do echo $category_1;qiime composition ancom --i-table exported/ANCOM/composition.${tax_levels[${n2}]}.qza --m-metadata-file $mapping_file --m-metadata-column $category_1 --o-visualization exported/ANCOM/${category_1}.ANCOM.${tax_levels[${n2}]}.qzv;done;
#qiime composition ancom --i-table exported/ANCOM/composition.${tax_levels[${n2}]}.qza --m-metadata-file $mapping_file --m-metadata-column $category_2 --o-visualization exported/ANCOM/SecondaryGroup/ANCOM.${tax_levels[${n2}]}.qzv;
done;
echo "##############################################################\n#Run for PICRUST analysis and STAMP visulization"
qiime vsearch cluster-features-closed-reference --i-sequences rep-seqs.qza --i-table table.qza --i-reference-sequences $close_reference_trained --p-perc-identity 0.97 --p-threads 0 --output-dir closedRef_forPICRUSt
qiime feature-table summarize --i-table closedRef_forPICRUSt/clustered_table.qza --o-visualization closedRef_forPICRUSt/clustered_table.qzv --m-sample-metadata-file $mapping_file
qiime feature-table tabulate-seqs --i-data closedRef_forPICRUSt/unmatched_sequences.qza --o-visualization closedRef_forPICRUSt/unmatched_sequences.qzv
qiime tools export --input-path closedRef_forPICRUSt/clustered_table.qza --output-path closedRef_forPICRUSt/
biom convert -i closedRef_forPICRUSt/feature-table.biom -o closedRef_forPICRUSt/feature-table.txt --to-tsv
source deactivate
source activate qm2
normalize_by_copy_number.py -i closedRef_forPICRUSt/feature-table.biom -o closedRef_forPICRUSt/feature-table.normalized.biom
predict_metagenomes.py -i closedRef_forPICRUSt/feature-table.normalized.biom -o closedRef_forPICRUSt/feature-table.metagenome.biom
categorize_by_function.py -i closedRef_forPICRUSt/feature-table.metagenome.biom -o closedRef_forPICRUSt/feature-table.metagenome.L1.txt -c KEGG_Pathways -l 1 -f
categorize_by_function.py -i closedRef_forPICRUSt/feature-table.metagenome.biom -o closedRef_forPICRUSt/feature-table.metagenome.L2.txt -c KEGG_Pathways -l 2 -f
categorize_by_function.py -i closedRef_forPICRUSt/feature-table.metagenome.biom -o closedRef_forPICRUSt/feature-table.metagenome.L3.txt -c KEGG_Pathways -l 3 -f
cd closedRef_forPICRUSt
for n3 in 1 2 3;
do echo $n3;
python ${SCRIPTPATH}/convert_percent.py -i feature-table.metagenome.L${n3}.txt;
perl ${SCRIPTPATH}/get_table_head2.pl percent.feature-table.metagenome.L${n3}.txt 35 -trantab > percent.feature-table.metagenome.L${n3}.tab
perl ${SCRIPTPATH}/top10_bar_diagram.pl -right -grid -rotate='-45' -x_title 'Sample Name' -y_title 'Relative Abundance' --y_mun 0.25,4 --height 350 -table percent.feature-table.metagenome.L${n3}.tab > percent.feature-table.metagenome.L${n3}.svg
perl ${SCRIPTPATH}/cluster.pl -BC -Z -x percent.feature-table.metagenome.L${n3}.txt > level1.relative.tree
perl ${SCRIPTPATH}/draw_tree.pl -bun 0.25,4 -bline -type 4 level1.relative.tree percent.feature-table.metagenome.L${n3}.tab --flank_x 100 > tree.feature-table.metagenome.L${n3}.svg
#${SCRIPTPATH}/PCA.R.pl ${PWD}/percent.feature-table.metagenome.L${n3}.txt 0.2 ${PWD}/PCA_L${n3}
cp $mapping_file ./sample-metadata.PCA.txt
perl -p -i.bak -e 's/#//' ./sample-metadata.PCA.txt
tail -n +2 feature-table.metagenome.L${n3}.txt > feature-table.metagenome.L${n3}.PCA.txt
perl -p -i.bak -e 's/#OTU ID/KEGG_function/' feature-table.metagenome.L${n3}.PCA.txt
done;
for svg_file in *svg; do echo $svg_file; base=$(basename $svg_file .svg); rsvg-convert -h 3200 $svg_file > ${base}.png; done
cd ..
source deactivate
source activate qiime2-2018.8
echo "##############################################################\n#Make phylogenetic trees for ITOL"
mkdir phylogeny
qiime feature-table filter-features --i-table table.qza --p-min-frequency $min_freq --o-filtered-table phylogeny/table.${min_freq}.qza
qiime tools export --input-path phylogeny/table.${min_freq}.qza --output-path phylogeny
biom convert -i phylogeny/feature-table.biom -o phylogeny/feature-table.txt --to-tsv
cut -f1 phylogeny/feature-table.txt | tail -n +3 > phylogeny/feature-table.list
seqtk subseq exported/dna-sequences.fasta phylogeny/feature-table.list > phylogeny/dna-sequences.${min_freq}.fasta
qiime tools import --input-path phylogeny/dna-sequences.${min_freq}.fasta --output-path phylogeny/dna-sequences.${min_freq}.qza --type 'FeatureData[Sequence]'
qiime alignment mafft --i-sequences phylogeny/dna-sequences.${min_freq}.qza --o-alignment phylogeny/dna-sequences.${min_freq}.aligned.qza
qiime alignment mask --i-alignment phylogeny/dna-sequences.${min_freq}.aligned.qza --o-masked-alignment phylogeny/dna-sequences.${min_freq}.aligned.masked.qza
qiime phylogeny fasttree --i-alignment phylogeny/dna-sequences.${min_freq}.aligned.masked.qza --o-tree phylogeny/dna-sequences.${min_freq}.unrooted-tree.qza
qiime phylogeny midpoint-root --i-tree phylogeny/dna-sequences.${min_freq}.unrooted-tree.qza --o-rooted-tree phylogeny/dna-sequences.${min_freq}.rooted-tree.qza
qiime feature-classifier classify-sklearn --i-classifier $reference_trained --i-reads phylogeny/dna-sequences.${min_freq}.qza --o-classification phylogeny/taxonomy.${min_freq}.qza
biom add-metadata -i phylogeny/feature-table.biom -o phylogeny/feature-table.taxonomy.biom --observation-metadata-fp exported/taxonomy.tsv --observation-header OTUID,taxonomy,confidence
biom convert -i phylogeny/feature-table.taxonomy.biom -o phylogeny/feature-table.taxonomy.txt --to-tsv --header-key taxonomy
qiime tools export --input-path phylogeny/dna-sequences.${min_freq}.rooted-tree.qza --output-path phylogeny/
mv phylogeny/tree.nwk phylogeny/tree.rooted.nwk
perl ${SCRIPTPATH}/generate_file_Itol.pl phylogeny/feature-table.taxonomy.txt
echo "##############################################################\n#export all qzv files into clickable folders"
#for f in $(find . -type f -name "*.qzv"); do echo $f; qiime tools export $f --output-dir ${f}.exported; done
for f in $(find . -type f -name "*.qzv"); do echo $f; base=$(basename $f .qzv); dir=$(dirname $f); new=${dir}/${base}; qiime tools export --input-path $f --output-path ${new}.qzv.exported; done
echo "##############################################################\n#Run Qiime1 for differOTU analysis"
source deactivate
source activate qm1
mkdir exported/DiffAbundance
biom convert -i exported/Relative/otu_table.even.txt -o exported/DiffAbundance/otu_table.even.biom --to-hdf5 --table-type="OTU table" --process-obs-metadata taxonomy
summarize_taxa.py -i exported/DiffAbundance/otu_table.even.biom -a -o exported/DiffAbundance/tax
summarize_taxa.py -i exported/DiffAbundance/otu_table.even.biom -a -L 7 -o exported/DiffAbundance/tax
source ~/.bash_profile
for n4 in 2 3 4 5 6 7;
do echo $n4;
#the biom file should include taxonomy information for group_significance.py script
cut -f1 exported/DiffAbundance/tax/otu_table.even_L${n4}.txt > exported/DiffAbundance/tax/otu_table.even_L${n4}.1stColumn.txt
perl -p -i.bak -e 's/#OTU ID/taxonomy/' exported/DiffAbundance/tax/otu_table.even_L${n4}.1stColumn.txt
paste exported/DiffAbundance/tax/otu_table.even_L${n4}.txt exported/DiffAbundance/tax/otu_table.even_L${n4}.1stColumn.txt > exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.txt
biom convert -i exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.txt -o exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.biom --to-hdf5 --table-type="OTU table" --process-obs-metadata taxonomy
for category_1 in $category_set;
do echo $category_1;
group_significance.py -i exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.biom -m $mapping_file -c $category_1 -s kruskal_wallis -o exported/DiffAbundance/kruskal_wallis_${category_1}_DiffAbundance_${tax_levels[${n4}]}.txt --biom_samples_are_superset --print_non_overlap;
#group_significance.py -i exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.biom -m $mapping_file -c $category_2 -s kruskal_wallis -o exported/DiffAbundance/kruskal_wallis_${category_2}_DiffAbundance_${tax_levels[${n4}]}.txt --biom_samples_are_superset --print_non_overlap
group_significance.py -i exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.biom -m $mapping_file -c $category_1 -s ANOVA -o exported/DiffAbundance/ANOVA_${category_1}_DiffAbundance_${tax_levels[${n4}]}.txt --biom_samples_are_superset --print_non_overlap;
#group_significance.py -i exported/DiffAbundance/tax/otu_table.even_${tax_levels[${n4}]}.taxonomy.biom -m $mapping_file -c $category_2 -s ANOVA -o exported/DiffAbundance/ANOVA_${category_2}_DiffAbundance_${tax_levels[${n4}]}.txt --biom_samples_are_superset --print_non_overlap
python ${SCRIPTPATH}/auto_DESeq.py -m $mapping_file -g $category_1 -l ${tax_levels[${n4}]};
done;
done;
echo "##############################################################\n#Run R script for additional R related figure generation"
source deactivate
source activate qm2
mkdir R_output
#Change format of meta-data file for Rscript of PLSDA analysis
cp $mapping_file ./R_output/sample-metadata.txt
tail -n +2 exported/feature-table.txt > ./R_output/feature-table.PLSDA.txt
perl -p -i.bak -e 's/#OTU ID//' ./R_output/feature-table.PLSDA.txt
sort ./R_output/sample-metadata.txt > ./R_output/sample-metadata.PLSDA.txt
#Change format of meta-data file for Rscript of alpha diversity analysis
cp $mapping_file ./alpha/sample-metadata_alphadiversity.txt
perl -p -i.bak -e 's/#SampleID//' ./alpha/sample-metadata_alphadiversity.txt
for category_1 in $category_set;
do echo $category_1;
Rscript ${SCRIPTPATH}/RRelatedOutput.R $mapping_file $category_1;
Rscript ${SCRIPTPATH}/alphaboxplotwitSig.R ./alpha/sample-metadata_alphadiversity.txt $category_1 ./alpha/alpha-summary.tsv ./alpha/;
done;
perl ${SCRIPTPATH}/table_data_svg.pl --colors cyan-orange R_output/bray_matrix.txt R_output/wunifrac_matrix.txt R_output/unifrac_matrix.txt --symbol 'Beta Diversity' > R_output/BetaDiversity_heatmap.svg
rsvg-convert -h 3200 R_output/BetaDiversity_heatmap.svg > R_output/BetaDiversity_heatmap.png
python2 ${SCRIPTPATH}/biom_to_stamp.py -m KEGG_Pathways closedRef_forPICRUSt/feature-table.metagenome.biom > closedRef_forPICRUSt/feature-table.metagenome.KEGG_Pathways.STAMP.txt
for n5 in 1 2 3;
do echo $n5;
for category_1 in $category_set;do echo $category_1;Rscript ${SCRIPTPATH}/Function_PCA.r ${PWD}/closedRef_forPICRUSt/feature-table.metagenome.L${n5}.PCA.txt ${PWD}/closedRef_forPICRUSt//sample-metadata.PCA.txt $category_1;done;
done;
echo "##############################################################\n#Generate the absolute directory for enviromental factors relational analysis"
cd exported/
perl ${SCRIPTPATH}/stat_otu_tab.pl -unif min feature-table.taxonomy.txt --prefix Absolute/otu_table -nomat -abs -spestat Absolute/classified_stat.xls
cd Absolute
for key in ${!tax_aa[*]};do mv otu_table.${key}.absolute.mat otu_table.${tax_aa[$key]}.absolute.txt;done;
#mv otu_table.k.absolute.mat otu_table.Kingdom.absolute.txt
#mv otu_table.p.absolute.mat otu_table.Pylumn.absolute.txt
#mv otu_table.c.absolute.mat otu_table.Class.absolute.txt
#mv otu_table.o.absolute.mat otu_table.Order.absolute.txt
#mv otu_table.f.absolute.mat otu_table.Family.absolute.txt
#mv otu_table.g.absolute.mat otu_table.Genus.absolute.txt
#mv otu_table.s.absolute.mat otu_table.Species.absolute.txt
mkdir RDA
for n6 in "Phylum" "Class" "Order" "Family" "Genus" "Species";
do echo $n6;
mkdir RDA/${n6}
cp otu_table.${n6}.absolute.txt RDA/${n6}
cd RDA/${n6}
for category_1 in $category_set;do echo $category_1;python ${SCRIPTPATH}/RDA.py -i otu_table.${n6}.absolute.txt -m $mapping_file -g $category_1 -o ./ -n 20 -e $not_rda;done;
cd ../../
done;
cd ../../
echo "#############################################################\nAdditional plot"
mkdir 4-VennAndFlower
for category_1 in $category_set;
do echo $category_1;
Rscript ${SCRIPTPATH}/venn_and_flower_plot.R ./exported/feature-table.taxonomy.txt $mapping_file $category_1 ./4-VennAndFlower 0;
python ${SCRIPTPATH}/phylotree_and_heatmap.py -i ./exported/feature-table.taxonomy.txt -m $mapping_file -g $category_1 -r masked-aligned-rep-seqs.qza -o AdditionalPhylogeny/ -n 30
done;
echo "##############################################################\nCorrelation analysis"
for n7 in "Phylum" "Class" "Order" "Family" "Genus" "Species";
do echo $n7;
Rscript ${SCRIPTPATH}/network.R -c 0.5 -i exported/Relative/otu_table.${n7}.relative.txt -o 3-NetworkAnalysis/${n7}/;
Rscript ${SCRIPTPATH}/cor_heatmap.R -i exported/Relative/otu_table.${n7}.relative.txt -o 2-CorrelationHeatmap/${n7}/ -n 20 -m $mapping_file -e $not_rda;
done;
echo "##############################################################\n#Run LEFSE for Group"
source deactivate
source activate LEFSE
cd exported/Relative
mkdir Lefse/
for n7 in "Phylum" "Class" "Order" "Family" "Genus" "Species";
do echo $n7;
mkdir Lefse/${n7}
cp otu_table.${n7}.relative.txt Lefse/${n7}
cd Lefse/${n7}
for category_1 in $category_set;
do echo $category_1;
Rscript ${SCRIPTPATH}/write_data_for_lefse.R otu_table.${n7}.relative.txt $mapping_file $category_1 ${category_1}_${n7}_lefse.txt;
base=$(basename ${category_1}_${n7}_lefse.txt .txt); format_input.py ${base}.txt ${base}.lefseinput.txt -c 2 -u 1 -o 1000000; run_lefse.py ${base}.lefseinput.txt ${base}.LDA.txt; plot_res.py --dpi 300 ${base}.LDA.txt ${base}.png; plot_cladogram.py ${base}.LDA.txt --dpi 300 ${base}.cladogram.png --format png --right_space_prop 0.4 --label_font_size 10;
done;
cd ../../
done;
cd ../../
echo "##############################################################\n#Organize the result files"
#cp -r ${SCRIPTPATH}/Result_AmpliconSequencing ./
sh ${SCRIPTPATH}/organize_dir_structure_V2.sh $mapping_file $category_report ${SCRIPTPATH} $min_freq
com2
}
MAIN;