179775232ff5fe31323f984619b75cbc77204c00
angie
  Sun Jun 27 20:22:29 2021 -0700
Update nextclade to 1.0 (new required command line args).

diff --git src/hg/utils/otto/sarscov2phylo/getNcbi.sh src/hg/utils/otto/sarscov2phylo/getNcbi.sh
index 2ee7749..385deb7 100755
--- src/hg/utils/otto/sarscov2phylo/getNcbi.sh
+++ src/hg/utils/otto/sarscov2phylo/getNcbi.sh
@@ -1,156 +1,167 @@
 #!/bin/bash
 source ~/.bashrc
 set -beEu -x -o pipefail
 
 # Download SARS-CoV-2 GenBank FASTA and metadata using NCBI Datasets API.
 # Use E-Utils to get SARS-CoV-2 metadata from BioSample.
 # Use BioSample metadata to fill in gaps in GenBank metadata and report conflicting dates.
 # Use enhanced metadata to rewrite FASTA headers for matching up with sequences in other databases.
 
 scriptDir=$(dirname "${BASH_SOURCE[0]}")
 source $scriptDir/util.sh
 
 today=$(date +%F)
 
 ottoDir=/hive/data/outside/otto/sarscov2phylo
 
 mkdir -p $ottoDir/ncbi.$today
 cd $ottoDir/ncbi.$today
 
 datasets download virus genome taxon 2697049 \
     --exclude-cds \
     --exclude-protein \
     --exclude-gpff \
     --exclude-pdb \
     --filename ncbi_dataset.zip \
 |& tail -50 \
     > datasets.log
 rm -rf ncbi_dataset
 unzip ncbi_dataset.zip
 # Creates ./ncbi_dataset/
 
 # This makes something just like ncbi.datasets.tsv from the /table/ API query:
 jq -c -r '[.accession, .biosample, .isolate.collectionDate, .location.geographicLocation, .host.sciName, .isolate.name, .completeness, (.length|tostring)] | join("\t")' \
     ncbi_dataset/data/data_report.jsonl \
 | sed -e 's/COMPLETE/complete/; s/PARTIAL/partial/;' \
 | sort \
     > ncbi_dataset.tsv
 
 # Use EUtils (esearch) to get all SARS-CoV-2 BioSample GI# IDs:
 $scriptDir/searchAllSarsCov2BioSample.sh
 sort all.biosample.gids.txt > all.biosample.gids.sorted.txt
 
 # Copy yesterday's all.bioSample.txt so we don't have to refetch all the old stuff.
 if [ -e ../ncbi.latest/all.bioSample.txt.xz ]; then
     xzcat ../ncbi.latest/all.bioSample.txt.xz > all.bioSample.txt
     grep ^Accession all.bioSample.txt | sed -re 's/^.*ID: //' | sort -u > ids.loaded
     comm -23 all.biosample.gids.sorted.txt ids.loaded > ids.notLoaded
 elif [ -e ../ncbi.latest/all.bioSample.txt ]; then
     cp ../ncbi.latest/all.bioSample.txt all.bioSample.txt
     grep ^Accession all.bioSample.txt | sed -re 's/^.*ID: //' | sort -u > ids.loaded
     comm -23 all.biosample.gids.sorted.txt ids.loaded > ids.notLoaded
 else
     cp -p all.biosample.gids.txt ids.notLoaded
 fi
 wc -l ids.notLoaded
 
 # Use EUtils (efetch) to get BioSample records for the GI# IDs that we don't have yet:
 time $scriptDir/bioSampleIdToText.sh < ids.notLoaded >> all.bioSample.txt
 
 grep ^Accession all.bioSample.txt | sed -re 's/^.*ID: //' | sort > ids.loaded
 comm -23 all.biosample.gids.sorted.txt ids.loaded > ids.notLoaded
 if [ -s ids.notLoaded ]; then
     echo Retrying queries for `wc -l < ids.notLoaded` IDs
     $scriptDir/bioSampleIdToText.sh < ids.notLoaded >> all.bioSample.txt
     grep ^Accession all.bioSample.txt | sed -re 's/^.*ID: //' | sort > ids.loaded
     comm -23 all.biosample.gids.sorted.txt ids.loaded > ids.notLoaded
     if [ -s ids.notLoaded ]; then
         echo "Still have only $accCount accession lines after retrying; quitting."
         exit 1
     fi
 fi
 
 # Extract properties of interest into tab-sep text:
 $scriptDir/bioSampleTextToTab.pl < all.bioSample.txt  > all.bioSample.tab
 
 # Extract BioSample tab-sep lines just for BioSample accessions included in the ncbi_dataset data:
 tawk '$2 != "" {print $2;}' ncbi_dataset.tsv \
 | grep -Fwf - all.bioSample.tab \
     > gb.bioSample.tab
 
 # Use BioSample metadata to fill in missing pieces of GenBank metadata and report conflicting
 # sample collection dates:
 $scriptDir/gbMetadataAddBioSample.pl gb.bioSample.tab ncbi_dataset.tsv \
     > ncbi_dataset.plusBioSample.tsv
 
 # Make a file for joining collection date with ID:
 tawk '$3 != "" {print $1, $3;}' ncbi_dataset.plusBioSample.tsv \
 | sort > gbToDate
 
 # Replace FASTA headers with reconstructed names from enhanced metadata.
 time cleanGenbank < ncbi_dataset/data/genomic.fna \
 | $scriptDir/fixNcbiFastaNames.pl ncbi_dataset.plusBioSample.tsv \
 | xz -T 50 \
     > genbank.fa.xz
 
 # Run pangolin and nextclade on sequences that are new since yesterday
 fastaNames genbank.fa.xz | awk '{print $1;}' | sed -re 's/\|.*//' | sort > gb.names
 splitDir=splitForNextclade
 rm -rf $splitDir
 mkdir $splitDir
 if [ -e ../ncbi.latest/nextclade.tsv ]; then
     cp ../ncbi.latest/nextclade.tsv .
     cut -f 1 ../ncbi.latest/nextclade.tsv | sort > nextclade.prev.names
     comm -23 gb.names nextclade.prev.names > nextclade.names
     faSomeRecords <(xzcat genbank.fa.xz) nextclade.names nextclade.fa
     faSplit about nextclade.fa 30000000 $splitDir/chunk
 else
     cp /dev/null nextclade.tsv
     faSplit about <(xzcat genbank.fa.xz) 30000000 $splitDir/chunk
 fi
+nDataDir=~angie/github/nextclade/data/sars-cov-2
+outDir=$(mktemp -d)
+outTsv=$(mktemp)
 for chunkFa in $splitDir/chunk*.fa; do
-    nextclade -j 50 -i $chunkFa -t >(cut -f 1,2 | tail -n+2 >> nextclade.tsv) >& nextclade.log
+    nextclade -j 50 -i $chunkFa \
+        --input-root-seq $nDataDir/reference.fasta \
+        --input-tree $nDataDir/tree.json \
+        --input-qc-config $nDataDir/qc.json \
+        --output-dir $outDir \
+        --output-tsv $outTsv >& nextclade.log
+    cut -f 1,2 $outTsv | tail -n+2 >> nextclade.tsv
+    rm $outTsv
 done
 wc -l nextclade.tsv
+rm -rf $outDir
 rm -rf $splitDir nextclade.fa
 
 conda activate pangolin
 runPangolin() {
     fa=$1
     out=$fa.pangolin.csv
     logfile=$(mktemp)
     pangolin $fa --outfile $out > $logfile 2>&1
     rm $logfile
 }
 export -f runPangolin
 if [ -e ../ncbi.latest/lineage_report.csv ]; then
     cp ../ncbi.latest/lineage_report.csv linRepYesterday
     tail -n+2 linRepYesterday | sed -re 's/^([A-Z]+[0-9]+\.[0-9]+).*/\1/' | sort \
         > pangolin.prev.names
     comm -23 gb.names pangolin.prev.names > pangolin.names
     faSomeRecords <(xzcat genbank.fa.xz) pangolin.names pangolin.fa
     pangolin pangolin.fa >& pangolin.log
     tail -n+2 lineage_report.csv >> linRepYesterday
     mv linRepYesterday lineage_report.csv
     rm -f pangolin.fa
 else
     splitDir=splitForPangolin
     rm -rf $splitDir
     mkdir $splitDir
     faSplit about <(xzcat genbank.fa.xz) 30000000 $splitDir/chunk
     find $splitDir -name chunk\*.fa \
     | parallel -j 10 "runPangolin {}"
     head -1 $(ls -1 $splitDir/chunk*.csv | head -1) > lineage_report.csv
     for f in $splitDir/chunk*.csv; do
         tail -n+2 $f >> lineage_report.csv
     done
     rm -rf $splitDir
 fi
 wc -l lineage_report.csv
 
 rm -f $ottoDir/ncbi.latest
 ln -s ncbi.$today $ottoDir/ncbi.latest
 
 # Clean up
 rm -r ncbi_dataset
 nice xz all.bioSample.* &