src/hg/makeDb/doc/ferrAcid1.txt 1.3

1.3 2009/11/25 21:48:39 hiram
change autoScaleDefault to autoScale
Index: src/hg/makeDb/doc/ferrAcid1.txt
===================================================================
RCS file: /projects/compbio/cvsroot/kent/src/hg/makeDb/doc/ferrAcid1.txt,v
retrieving revision 1.2
retrieving revision 1.3
diff -b -B -U 1000000 -r1.2 -r1.3
--- src/hg/makeDb/doc/ferrAcid1.txt	26 Jul 2006 16:59:54 -0000	1.2
+++ src/hg/makeDb/doc/ferrAcid1.txt	25 Nov 2009 21:48:39 -0000	1.3
@@ -1,361 +1,361 @@
 # for emacs: -*- mode: sh; -*-
 
  
 # This file describes building the browser database for the archaeal
 # species Methanosarcina acetivorans.
 #
 # if this is the first time you are making your own hgwdev browser, need to do 
 # cd ~/kent/src/, then a make
 
 # DOWNLOAD SEQUENCE FROM GENBANK (DONE 10/2/05)
 
     mkdir /cluster/store5/archae/ferrAcid1
     ln -s /cluster/store5/archae/ferrAcid1 /cluster/data/ferrAcid1
     cd /cluster/data/ferrAcid1
     cp /projects/lowelab/db/Bacteria/Ferroplasma_acidarmanus/Ferr_acid* .
     mv Ferr_acid.fa ferrAcid1.fa
     grep ">" ferrAcid1.fa
     # Edit header of ferrAcid1.fa seqs to '>chr >plasmid_pNRC100 >plasmid_pNRC200'
    
     faToTwoBit ferrAcid1.fa ferrAcid1.2bit 
 
     mkdir /gbdb/ferrAcid1
     ln -s /cluster/data/ferrAcid1/ferrAcid1.2bit /gbdb/ferrAcid1/ferrAcid1.2bit
 
 # CREATE DATABASES AND A BUNCH OF INITIAL STUFF (DONE 10/2/05)
 
     ssh hgwdev
     echo 'create database ferrAcid1' | hgsql ''
     cd /cluster/data/ferrAcid1
 
     faSize -detailed ferrAcid1.fa > chrom.sizes
     echo "create table grp (PRIMARY KEY(NAME)) select * from hg16.grp" | hgsql ferrAcid1
     echo 'INSERT INTO dbDb (name, description, nibPath, organism, defaultPos, active, orderKey, genome, scientificName, htmlPath, hgNearOk) values ("ferrAcid1", "Jun 2005 Draft", "/gbdb/ferrAcid1", "Ferroplasma acidarmanus", "chr:500000-550000", 1, 280, "Ferroplasma acidarmanus","Ferroplasma acidarmanus Fer1", "/gbdb/ferrAcid1/html/description.html", 0);' | hgsql hgcentraltest
     echo 'INSERT INTO defaultDb (genome, name) values ("Ferroplasma acidarmanus", "ferrAcid1");' | hgsql hgcentraltest
     echo 'INSERT INTO genomeClade (genome, clade, priority) values ("Ferroplasma acidarmanus", "archaea",85);'  | hgsql hgcentraltest
 
 # CREATE CHROMINFO TABLE 
   ssh hgwdev
   cd /cluster/data/ferrAcid1
 
    cp ~baertsch/kent/src/hg/lib/chromInfo.sql .
    hgsql ferrAcid1 < chromInfo.sql
    echo "load data local infile 'chrom.sizes' into table chromInfo" | hgsql ferrAcid1
    echo "update chromInfo set fileName = '/gbdb/ferrAcid1/ferrAcid1.2bit'" | hgsql ferrAcid1
 
     cd ~/kent/src/hg/makeDb/trackDb
 
     # add the trackDb directories
     mkdir -p archae/ferrAcid1
     cvs add archae/ferrAcid1
     cvs commit archae/ferrAcid1
 
     make DBS=ferrAcid1
 
 
 # GC20BASE (DONE 10/2/05)
     mkdir -p /cluster/data/ferrAcid1/bed/gc20Base
     cd /cluster/data/ferrAcid1/bed/gc20Base
     hgGcPercent -wigOut -doGaps -file=stdout -overlap=10 -win=20 ferrAcid1 /cluster/data/ferrAcid1/ | wigEncode stdin gc20Base.wig gc20Base.wib
 
     cd /cluster/data/ferrAcid1/bed/gc20Base
     mkdir /gbdb/ferrAcid1/wib
     ln -s `pwd`/gc20Base.wib /gbdb/ferrAcid1/wib
     hgLoadWiggle -pathPrefix=/gbdb/ferrAcid1/wib ferrAcid1 gc20Base gc20Base.wig
     #	verify index is correct:
     hgsql ferrAcid1 -e "show index from gc20Base;"
     #	should see good numbers in Cardinality column
 
 
 # TANDEM REPEAT MASKER (DONE 10/2/05)
 
     ssh hgwdev
     mkdir -p /cluster/data/ferrAcid1/bed/simpleRepeat
     cd /cluster/data/ferrAcid1
     trfBig ferrAcid1.fa /dev/null -bedAt=/cluster/data/ferrAcid1/bed/simpleRepeat/chr.bed
     cd /cluster/data/ferrAcid1/bed/simpleRepeat
     hgLoadBed ferrAcid1 simpleRepeat *.bed -sqlTable=/cluster/home/lowe/kent/src/hg/lib/simpleRepeat.sql
 
 # NO TIGR GENES
 # genome not available at http://www.tigr.org/tigr-scripts/CMR2/gene_attribute_form.dbi
 
 # DESCRIPTION PAGE (DONE 10/4/05)
 
     # Write ~/kent/src/hg/makeDb/trackDb/archae/ferrAcid1/description.html
     chmod a+r ~/kent/src/hg/makeDb/trackDb/archae/ferrAcid1/description.html
     mkdir -p /cluster/data/ferrAcid1/html/
     cp ~/kent/src/hg/makeDb/trackDb/archae/ferrAcid1/description.html /cluster/data/ferrAcid1/html/description.html
     mkdir -p /gbdb/ferrAcid1/html
     ln -s /cluster/data/ferrAcid1/html/description.html /gbdb/ferrAcid1/html/
 
 # MULTIZ with therAcid, therVolc, picrTorr
 # DONE (10/13/05), kpollard
 
     cd /cluster/data/ferrAcid1/bed/
     mkdir conservation
     cd conservation
     cp /cluster/data/metAce1/bed/conservation/HoxD55.q .
     cp ../../chr.fa ferrAcid1.chr
     sed s/Contig/ferrAcid1.Contig/ ferrAcid1.chr > temp
     mv temp ferrAcid1.chr
     cp /cluster/data/therAcid1/bed/conservation/therAcid1.chr .
     cp /cluster/data/picrTorr1/bed/conservation/picrTorr1.chr .
     cp /cluster/data/therVolc1/bed/conservation/therVolc1.chr .
     faToNib therVolc1.chr therVolc1.chr.nib
     faToNib therAcid1.chr therAcid1.chr.nib
     faToNib picrTorr1.chr picrTorr1.chr.nib
     faToTwoBit ferrAcid1.chr ferrAcid1.2bit
     #chrom sizes
     faSize -detailed *.chr > chrom.sizes
     #make fa for each contig
     faSplit byname ferrAcid1.chr ./
     ls ferrAcid1.Contig*.fa > contignames.txt
     cat contignames.txt | gawk '{print substr($1,11,length($1))}' > contigs.txt
     foreach f (`cat contignames.txt`)
 	set b=$f:r
 	cat $f | gawk '{if(/>ferrAcid1.Contig/){print $0;}else{print toupper($0);}}' > temp
 	mv temp $f
 	faToNib $f $b.nib
     end
 
     #blastz 
     foreach f (`cat contignames.txt`)
 	set b=$f:t:r
 	echo $b
 	blastz $f therAcid1.chr Q=HoxD55.q > ${b}-therAcid1.lav 
 	blastz $f picrTorr1.chr Q=HoxD55.q > ${b}-picrTorr1.lav
 	blastz $f therVolc1.chr Q=HoxD55.q > ${b}-therVolc1.lav
     end
 
     foreach f(*.lav)
         set b=$f:r
 	echo $b
 	lavToAxt $f . . $b.axt
     end
 
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	echo $b
 	axtBest ${b}-therAcid1.axt $b -winSize=500 -minScore=5000 ${b}-therAcid1-best.axt
 	axtBest ${b}-picrTorr1.axt $b -winSize=500 -minScore=5000 ${b}-picrTorr1-best.axt
 	axtBest ${b}-therVolc1.axt $b -winSize=500 -minScore=5000 ${b}-therVolc1-best.axt
     end
 
     foreach f(*-best.axt)
 	set b=`basename $f -best.axt`
 	echo $b
 	axtToMaf $f chrom.sizes chrom.sizes $b.maf
     end
      
     #multiz
     #remove extra header lines
     foreach f(*.maf)
 	cat $f | gawk 'BEGIN{getline; print $0; getline; getline; getline; getline;}{print $0;}' > temp
 	mv temp $f
     end
 
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	echo $b
 	multiz ${b}-therAcid1.maf ${b}-picrTorr1.maf - > ${b}-therAcid1-picrTorr1.maf
 	multiz ${b}-therVolc1.maf ${b}-therAcid1-picrTorr1.maf - > ${b}-therAcid1-picrTorr1-therVolc1.maf
     end
 
     #phyloHMM
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	echo $b
 	msa_view -i MAF -M $f -o SS ${b}-therAcid1-picrTorr1-therVolc1.maf > $b.ss
     end
     
     foreach f(`cat contigs.txt`)
 	set b=$f:r
 	cat ferrAcid1.$b.ss | gawk '{if(/^NAMES/){print "NAMES = ferrAcid1,therVolc1,therAcid1,picrTorr1";} else{print $0;}}' > temp
 	mv temp $b.ss
 	phyloFit -i SS ferrAcid1.$b.ss -t "(ferrAcid1,(picrTorr1,(therAcid1,therVolc1)))" -o ${b}_FaTaPtTv
     end
 
     #Contig 169 has the largest NTUPLES (1051) so use it for starting mod
     # it shows GC=0.205868+0.188380=0.394248
     #add GC content to next call
     foreach f(`cat contigs.txt`)
 	set b=$f:r
 	echo $b
 	phastCons ferrAcid1.$b.ss Contig169_FaTaPtTv.mod \
 	--gc 0.3942 --target-coverage 0.7 --estimate-trees ${b} \
 	--expected-lengths 25 --no-post-probs --ignore-missing \
 	--nrates 1,1
     end
 
     #average with phyloBoot to get cons.mod and noncons.mod
     #ls *.cons.mod > cons.txt
     #phyloBoot --read-mods '*cons.txt' --output-average ave.cons.mod > cons_summary.txt
     #ls *.noncons.mod > noncons.txt
     #phyloBoot --read-mods '*noncons.txt' --output-average ave.noncons.mod > noncons_summary.txt
     #PROBLEM: Can't do this with different numbers of species in each mod
     #Again, just use Contig169 model
 
     #get rid of SS files with no data
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	wc -l $b.ss | gawk '{if($1==0){print "rm "$2}}' >> rmjobs
     end
     chmod +x rmjobs
     rmjobs
 
     foreach f(*.cons.mod)
 	set b=$f:r:r
 	echo $b
 	phastCons $b.ss Contig169.cons.mod,Contig169.noncons.mod \
 	--target-coverage 0.7 --expected-lengths 25 \
 	--viterbi ${b}_ferrAcid1-elements.bed --score \
 	--require-informative 0 --seqname $b > ${b}_cons.dat
 	wigEncode ${b}_cons.dat ${b}_phastCons.wig ${b}_phastCons.wib
     end
 
     #combine phastCons elements into 1 bed file
     cat Contig*.bed > phastCons.bed
 
     #move data
     mkdir wib
     mv Contig*_phastCons.wib wib/.
     mv Contig*_phastCons.wig wib/.
     ln -s /cluster/data/ferrAcid1/bed/conservation/wib/*.wib /gbdb/ferrAcid1/wib
     mkdir /gbdb/ferrAcid1/pwMaf
     mkdir -p otherSpp/therAcid1 otherSpp/picrTorr1 otherSpp/therVolc1
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	echo $b
 	mv ferrAcid1.${b}-picrTorr1.maf otherSpp/picrTorr1/$b.maf
 	mv ferrAcid1.${b}-therAcid1.maf otherSpp/therAcid1/$b.maf
 	mv ferrAcid1.${b}-therVolc1.maf otherSpp/therVolc1/$b.maf
     end
     ln -s /cluster/data/ferrAcid1/bed/conservation/otherSpp/picrTorr1 /gbdb/ferrAcid1/pwMaf/picrTorr1_pwMaf
     ln -s /cluster/data/ferrAcid1/bed/conservation/otherSpp/therVolc1 /gbdb/ferrAcid1/pwMaf/therVolc1_pwMaf
     ln -s /cluster/data/ferrAcid1/bed/conservation/otherSpp/therAcid1 /gbdb/ferrAcid1/pwMaf/therAcid1_pwMaf
     mkdir multiz
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	echo $b
 	mv ferrAcid1.${b}-therAcid1-picrTorr1-therVolc1.maf multiz/$b.maf
     end
     ln -s /cluster/data/ferrAcid1/bed/conservation/multiz /gbdb/ferrAcid1/multizFaTaPtTv
     #get rid of wig files with no data
     rm rmjobs
     foreach f(`cat contignames.txt`)
 	set b=$f:r
 	wc -l wib/${b}_phastCons.wig | gawk '{if($1==0){print "rm "$2}}' >> rmjobs
     end
     chmod +x rmjobs
     rmjobs
 
     #load
     hgLoadWiggle ferrAcid1 phastCons /cluster/data/ferrAcid1/bed/conservation/wib/Contig*_phastCons.wig
     hgLoadMaf -warn ferrAcid1 multizFaTaPtTv
     hgLoadMaf -warn ferrAcid1 picrTorr1_pwMaf -pathPrefix=/gbdb/ferrAcid1/pwMaf/picrTorr1_pwMaf
     hgLoadMaf -warn ferrAcid1 therVolc1_pwMaf -pathPrefix=/gbdb/ferrAcid1/pwMaf/therVolc1_pwMaf
     hgLoadMaf -warn ferrAcid1 therAcid1_pwMaf -pathPrefix=/gbdb/ferrAcid1/pwMaf/therAcid1_pwMaf
     hgLoadBed ferrAcid1 phastConsElements phastCons.bed 
 
     #trackDb
     cd ~/kent/src/hg/makeDb/trackDb/archae/ferrAcid1
     #trackDb.ra entry
     # track multizFaTaPtTv
     # shortLabel Conservation
     # longLabel Methanogen multiz alignments
     # group compGeno
     # priority 10.0
     # visibility pack
     # type wigMaf 0.0 1.0
     # maxHeightPixels 100:40:11
     # wiggle phastCons
     # yLineOnOff Off
-    # autoScaleDefault Off
+    # autoScale Off
     # pairwise pwMaf
     # speciesOrder therAcid1 picrTorr1 therVolc1
     cvs add trackDb.ra
     cvs commit -m "New multiz track" trackDb.ra
     #html page
     cvs add multizFaTaPtTv.html
     cvs commit -m "Details page for multiz track" multizFaTaPtTv.html
 
 
 # GENBANK PROTEIN-CODING GENES ()
 
     ssh hgwdev
     mkdir /cluster/data/ferrAcid1/genbank
     cd /cluster/data/ferrAcid1/genbank
     cp /projects/lowelab/db/Bacteria/Ferroplasma_acidarmanus/ .
     
     mv NC_003552.gbk ferrAcid1.gbk
     # Create 3 files to assist parsing of the genbank
     # 1. for a bed file
     echo 'chr
 start
 end
 gene
 1000
 strand' > ferrAcid1-params-bed.txt
     # 2. for the peptide parts
     echo 'gene
 translation' > ferrAcid1-params-pep.txt
     # 3. for the other gene information
     echo 'gene
 product
 note' > ferrAcid1-params-xra.txt
     # Now extract the genes and information:
     gbArchaeGenome ferrAcid1.gbk ferrAcid1-params-bed.txt ferrAcid1-genbank-cds.bed
     gbArchaeGenome ferrAcid1.gbk ferrAcid1-params-pep.txt ferrAcid1-genbank-cds.pep
     gbArchaeGenome ferrAcid1.gbk ferrAcid1-params-xra.txt ferrAcid1-genbank-cds.xra
     hgLoadBed ferrAcid1 gbProtCode ferrAcid1-genbank-cds.bed
     hgsql ferrAcid1 < ~/kent/src/hg/lib/pepPred.sql
     hgsql ferrAcid1 < ~/kent/src/hg/lib/minGeneInfo.sql
     echo rename table pepPred to gbProtCodePep | hgsql ferrAcid1
     echo rename table minGeneInfo to gbProtCodeXra | hgsql ferrAcid1
     echo load data local infile \'ferrAcid1-genbank-cds.pep\' into table gbProtCodePep | hgsql ferrAcid1
     echo load data local infile \'ferrAcid1-genbank-cds.xra\' into table gbProtCodeXra | hgsql ferrAcid1
 
 #genbank to genePred
 
 csh
 tawk '{print $1,$2,$3,$4,$5,$6,$2,$3,0,1,$3-$2,0}' ferrAcid1-genbank-cds.bed | bedToGenePred stdin tmp.gp
 tawk '{print $1,$2,$3,$4,$5,$6,$7,$8,$9,$10,substr($1,3,4),name2,"cmpl","cmpl",0}' tmp.gp  > tmp2.gp
 join -t "     " -o 1.1,1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 1.10 1.11 2.3 1.13 1.14 1.15  tmp2.gp ferrAcid1-genbank-cds.xra > ferrAcid1.gp
 
 # GENBANK rRNA GENES ()
     ssh hgdev
     cd /cluster/data/ferrAcid1/genbank
     gbArchaeGenome -kind=rRNA ferrAcid1.gbk ferrAcid1-params-bed.txt ferrAcid1-rrnas.bed
     echo 'gene product NA' > ferrAcid1-params-rrna-xra.txt
     gbArchaeGenome -kind=rRNA ferrAcid1.gbk ferrAcid1-params-rrna-xra.txt ferrAcid1-rrnas-xra.txt
     hgLoadBed ferrAcid1 gbRRNA ferrAcid1-rrnas.bed
     hgsql ferrAcid1 < ~/kent/src/hg/lib/minGeneInfo.sql
     echo rename table minGeneInfo to gbRRNAXra | hgsql ferrAcid1
     echo load data local infile \'ferrAcid1-rrnas-xra.txt\' into table gbRRNAXra | hgsql ferrAcid1
 
 # COG STUFF
     # Cut and paste http://www.ncbi.nlm.nih.gov/cgi-bin/COG/palox into emacs (COG list)
     # and save as cogpage.txt
     awk '{printf("%s\t%s\n",$6,$5)}' < cogpage.txt | sed -e 's/\[//' -e 's/\]//' > cogs.txt
     rm cogpage.txt
     # Now we have the basic list of cogs and the letter code for each one.
     
 
 # TODD LOWE tRNA GENES ()
 
     # This one is a bed 6+ file created by hand of 46 tRNAs and 1 pseudo tRNA by Todd
     # Lowe.  See ~/kent/src/hg/lib/loweTrnaGene.as for a description of the fields.
     # **Showing the tRNAScanSE instructions would be nice in the future.  
     ssh hgwdev
     mkdir /cluster/data/ferrAcid1/bed/loweTrnaGene
     cd /cluster/data/ferrAcid1/bed/loweTrnaGene
     hgLoadBed -tab ferrAcid1 loweTrnaGene ferrAcid1-lowe-trnas.bed -sqlTable=~/kent/src/hg/lib/loweTrnaGene.sql
 
 # TODD LOWE snoRNA GENES ()
     # This is a bed 6 file created by hand.
     ssh hgwdev
     mkdir /cluster/data/ferrAcid1/bed/loweSnoGene
     cd /cluster/data/ferrAcid1/bed/loweSnoGene
     hgLoadBed -tab ferrAcid1 loweSnoGene ferrAcid1-snos.bed