# for emacs: -*- mode: sh; -*- # Caenorhabditis remanei # From Wash U GSC # http://genome.wustl.edu/genome.cgi?GENOME=Caenorhabditis+remanei # http://www.ncbi.nlm.nih.gov/Traces/wgs/?val=AAGD02 # $Id: caeRem3.txt,v 1.6 2008/08/15 21:53:32 hiram Exp $ ######################################################################### # DOWNLOAD SEQUENCE (DONE - 2008-05-22 - Hiram) ssh kkstore01 mkdir /cluster/store10/caeRem3 ln -s /cluster/store10/caeRem3 /cluster/data/caeRem3 mkdir /cluster/data/caeRem3/downloads cd /cluster/data/caeRem3/downloads wget --timestamping \ ftp://genome.wustl.edu/pub/organism/Invertebrates/Caenorhabditis_remanei/assembly/Caenorhabditis_remanei-15.0.1/ASSEMBLY wget --timestamping \ "ftp://genome.wustl.edu/pub/organism/Invertebrates/Caenorhabditis_remanei/assembly/Caenorhabditis_remanei-15.0.1/output/README" \ -O README.caeRem3 wget --timestamping -m -np -nd \ "ftp://genome.wustl.edu/pub/organism/Invertebrates/Caenorhabditis_remanei/assembly/Caenorhabditis_remanei-15.0.1/output/" ########################################################################## ## Create chrUn.agp file (DONE - 2008-05-22 - Hiram) ssh kkstore01 cd /cluster/data/caeRem3/downloads faSize contigs.fa.gz # 138406388 bases (185 N's 138406203 real 138406203 upper 0 lower) # in 12680 sequences in 1 files faSize supercontigs.fa.gz # 145442736 bases (7036533 N's 138406203 real 138406203 upper 0 lower) # in 3670 sequences in 1 files # note the chrUnSize in the following, calculate from the faSize # on the supercontigs: # 145442736 + ( (3670 - 1) * 1000 ) = 149111736 cat << '_EOF_' > mkSuperLift.pl #!/usr/bin/env perl use strict; use warnings; my $start = 1; my $end = 1; my $itemCount = 1; my $agpItemCount = 1; my $curContig = ""; my $firstTime = 1; my $scaffoldGapSize = 1000; my $scafEnd = 1; my $superStart = 0; my $superEnd = 1; my $superLength = 0; my $chrUnSize = 149111736; my $chrUnName = "chrUn"; my $ctgFragCount = 1; open (CT,">caeRem3.ctgPos2.tab") or die "Can not write to caeRem3.ctgPos2.tab"; open (SC,">caeRem3.CtgScaf.agp") or die "Can not write to caeRem3.CtgScaf.agp"; open (AG,">caeRem3.chrUn.agp") or die "Can not write to caeRem3.chrUn.agp"; open (GL,">caeRem3.gold.tab") or die "Can not write to caeRem3.gold.tab"; open (FH,'zcat supercontigs.agp.gz|') or die "can not open zcat supercontigs.agp.gz"; while (my $line=) { chomp $line; if ($line =~ m/fragment/) { my ($name, $gStart, $gEnd, $gapCounter, $gapWN, $gapLen, $frag, $yesNo) = split('\s+',$line); $end = $start + $gapLen - 1; $scafEnd += $gapLen; printf SC "chrUn\t%d\t%d\t%d\t%s\t%d\t%s\t%s\n", $start, $end, $agpItemCount, $gapWN, $gapLen, $frag, $yesNo; printf AG "chrUn\t%d\t%d\t%d\t%s\t%d\t%s\t%s\n", $start, $end, $agpItemCount++, $gapWN, $gapLen, $frag, $yesNo; $start = $end + 1; } else { my ($ctgName, $ctgStart, $ctgEnd, $ctgCounter, $ctgWN, $name, $cStart, $cEnd, $strand) = split('\s+',$line); my $ctgLen = $ctgEnd - $ctgStart + 1; my $cLen = $cEnd - $cStart + 1; die "not matching start, end:\n$line" if ($ctgLen != $cLen); if (!$firstTime) { if ($ctgName ne $curContig) { $superLength = $superEnd - $superStart; $end = $start + $scaffoldGapSize - 1; printf SC "chrUn\t%d\t%d\t%d\tN\t%d\tscaffold\tno\n", $start, $end, $agpItemCount, $scaffoldGapSize; printf AG "chrUn\t%d\t%d\t%d\tN\t%d\tscaffold\tno\n", $start, $end, $agpItemCount++, $scaffoldGapSize; printf "%d\t%s\t%d\t%s\t%d\n", $superStart, $curContig, $superLength, $chrUnName, $chrUnSize; printf GL "%s\t%d\t%d\t%d\tW\t%s\t0\t%d\t+\n", $chrUnName, $superStart, $superEnd, $itemCount++, $curContig, $superLength; $start = $end + 1; $scafEnd = $cStart - 1; $superStart = $start - 1; $ctgFragCount = 1; } } else { $firstTime = 0; $scafEnd = 0; } $scafEnd += $ctgLen; my $fragStart = $scafEnd - $ctgLen + 1; $end = $start + $ctgLen - 1; $superEnd = $end; my $ctgFragName = sprintf("%s.%d", $ctgName, $ctgFragCount++); my $ctgFragStart = 1; my $ctgFragEnd = $scafEnd - $fragStart + 1; printf SC "chrUn\t%d\t%d\t%d\t%s\t%s\t%d\t%d\t%s\n", $start, $end, $agpItemCount, $ctgWN, $ctgFragName, $ctgFragStart, $ctgFragEnd, $strand; printf AG "chrUn\t%d\t%d\t%d\t%s\t%s\t%d\t%d\t%s\n", $start, $end, $agpItemCount++, $ctgWN, $ctgName, $fragStart, $scafEnd, $strand; printf CT "%s\t%d\tchrUn\t%d\t%d\tW\n", $name, $ctgLen, $start-1, $end; $start = $end + 1; $curContig = $ctgName; } } close (FH); close (AG); close (SC); $superLength = $superEnd - $superStart; printf "%d\t%s\t%d\t%s\t%d\n", $superStart, $curContig, $superLength, $chrUnName, $chrUnSize; printf GL "%s\t%d\t%d\t%d\tW\t%s\t0\t%d\t+\n", $chrUnName, $superStart, $superEnd, $itemCount++, $curContig, $superLength; close (GL); '_EOF_' # << happy emacs chmod +x mkSuperLift.pl ./mkSuperLift.pl > caeRem3.chrUn.lift qaToQac contigs.fa.qual.gz stdout \ | qacAgpLift caeRem3.CtgScaf.agp stdin chrUn.qac ########################################################################### ## Initial genome build (DONE - 2008-05-22 - Hiram) ssh kkstore01 cd /cluster/data/caeRem3 cat << '_EOF_' > caeRem3.config.ra # Config parameters for makeGenomeDb.pl: db caeRem3 clade worm genomeCladePriority 10 scientificName Caenorhabditis remanei commonName C. remanei assemblyDate Jul. 2007 assemblyLabel Washington University School of Medicine GSC C. remanei 15.0.1 orderKey 878 mitoAcc none fastaFiles /cluster/data/caeRem3/downloads/supercontigs.fa.gz agpFiles /cluster/data/caeRem3/downloads/caeRem3.chrUn.agp qualFiles /cluster/data/caeRem3/downloads/chrUn.qac dbDbSpeciesDir worm '_EOF_' # << happy emacs time nice -n +19 makeGenomeDb.pl caeRem3.config.ra \ > makeGenomeDb.out 2>&1 # real 4m14.263s ssh hgwdev cd /cluster/data/caeRem3/downloads sed -e "s/agpFrag/chrUn_gold/" $HOME/kent/src/hg/lib/agpFrag.sql \ > chrUn_gold.sql # edit that .sql file to add the bin column # bin smallint(6) NOT NULL default '0', # or, copy the one from caeRem2: cp /cluster/data/caeRem2/downloads/chrUn_gold.sql . hgLoadBed -sqlTable=chrUn_gold.sql caeRem3 chrUn_gold caeRem3.gold.tab hgLoadSqlTab caeRem3 ctgPos2 ~/kent/src/hg/lib/ctgPos2.sql \ caeRem3.ctgPos2.tab ########################################################################### ## Repeat Masker (DONE - 2008-05-22 - Hiram) ssh kkstore01 mkdir /cluster/data/caeRem3/bed/repeatMasker cd /cluster/data/caeRem3/bed/repeatMasker time nice -n +19 doRepeatMasker.pl caeRem3 \ -buildDir=/cluster/data/caeRem3/bed/repeatMasker > do.log 2>&1 # real 15m16.812s cd /cluster/data/caeRem3 twoBitToFa caeRem3.rmsk.2bit stdout | faSize stdin \ > caeRem3.rmsk.2bit.faSize cat caeRem3.rmsk.2bit.faSize # 149111736 bases (10705533 N's 138406203 real # 137196473 upper 1209730 lower) in 1 sequences in 1 files # %0.81 masked total, %0.87 masked real # we are not going to use this sequence, too little is masked, # instead, using the windowMasker business next # ln -s caeRem3.rmsk.2bit caeRem3.2bit # mkdir /san/sanvol1/scratch/worms/caeRem3 # cp -p caeRem3.2bit /san/sanvol1/scratch/worms/caeRem3 # cp -p chrom.sizes /san/sanvol1/scratch/worms/caeRem3 # cp -p downloads/caeRem3.chrUn.lift /san/sanvol1/scratch/worms/caeRem3 ########################################################################### ## Window Masker (DONE - 2008-05-22 - Hiram) ssh kolossus mkdir /cluster/data/caeRem3/bed/windowMasker cd /cluster/data/caeRem3/bed/windowMasker time nice -n +19 ~/kent/src/hg/utils/automation/doWindowMasker.pl \ -workhorse kolossus \ -buildDir=/cluster/data/caeRem3/bed/windowMasker caeRem3 > do.log 2>&1 # real 10m40.787s twoBitToFa caeRem3.wmsk.sdust.2bit stdout \ | faSize stdin > caeRem3.wmsk.sdust.2bit.faSize 2>&1 cat caeRem3.wmsk.sdust.2bit.faSize # 149111736 bases (10705533 N's 138406203 real # 96266616 upper 42139587 lower) in 1 sequences in 1 files # %28.26 masked total, %30.45 masked real ssh hgwdev cd /cluster/data/caeRem3/bed/windowMasker hgLoadBed caeRem3 windowmaskerSdust windowmasker.sdust.bed.gz # Loaded 1122372 elements of size 3 # eliminate the gaps from the masking (WM bug) featureBits caeRem3 -not gap -bed=notGap.bed # 138406388 bases of 138406388 (100.000%) in intersection time nice -n +19 featureBits caeRem3 windowmaskerSdust notGap.bed \ -bed=stdout | gzip -c > cleanWMask.bed.gz # 42139616 bases of 138406388 (30.446%) in intersection # reload track to get it clean hgLoadBed caeRem3 windowmaskerSdust cleanWMask.bed.gz # Loaded 1075009 elements of size 4 featureBits caeRem3 windowmaskerSdust # 42139616 bases of 138406388 (30.446%) in intersection ########################################################################### ## Simple Repeats (DONE - 2008-05-22 - Hiram) ssh titan screen # use a screen to manage this job mkdir /cluster/data/caeRem3/bed/simpleRepeat cd /cluster/data/caeRem3/bed/simpleRepeat time twoBitToFa ../../caeRem3.unmasked.2bit stdout \ | nice -n +19 trfBig -trf=/cluster/bin/i386/trf stdin /dev/null \ -bedAt=simpleRepeat.bed -tempDir=/scratch/tmp > do.out 2>&1 # real 43m39.381s awk '$5 <= 12' simpleRepeat.bed > trfMask.bed ssh hgwdev cd /cluster/data/caeRem3/bed/simpleRepeat nice -n +19 hgLoadBed caeRem3 simpleRepeat \ simpleRepeat.bed -sqlTable=$HOME/kent/src/hg/lib/simpleRepeat.sql # Loaded 39971 elements of size 16 featureBits caeRem3 simpleRepeat > fb.caeRem3.simpleRepeat.txt 2>&1 cat fb.caeRem3.simpleRepeat.txt # 5219673 bases of 138406388 (3.771%) in intersection ############################################################################## ## combine trf mask with windowmasker (DONE - 2008-05-23 - Hiram) ssh kkstore01 cd /cluster/data/caeRem3 zcat bed/windowMasker/cleanWMask.bed.gz \ | twoBitMask caeRem3.unmasked.2bit stdin \ -type=.bed caeRem3.cleanWMSdust.2bit cat bed/simpleRepeat/trfMask.bed \ | twoBitMask -add -type=.bed caeRem3.cleanWMSdust.2bit stdin caeRem3.2bit # can safely ignore the warning about BED file >= 13 fields # check it twoBitToFa caeRem3.2bit stdout | faSize stdin # 149111736 bases (10705533 N's 138406203 real 96215522 upper # 42190681 lower) in 1 sequences in 1 files # %28.29 masked total, %30.48 masked real # create gbdb symlink ssh hgwdev ln -s /cluster/data/caeRem3/caeRem3.2bit /gbdb/caeRem3 ############################################################################## ## create masked contigs for blastz (DONE - 2008-05-23 - Hiram) ssh kkstore01 mkdir /cluster/data/caeRem3/maskedContigs cd /cluster/data/caeRem3/maskedContigs # copy over lft2BitToFa.pl from /cluster/data/caePb2/jkStuff cp -p /cluster/data/caePb2/jkStuff/lft2BitToFa.pl ../jkStuff ln -s ../downloads/caeRem3.chrUn.lift . time nice -n +19 ../jkStuff/lft2BitToFa.pl \ ../caeRem3.2bit caeRem3.chrUn.lift > super.fa # real 1m40.247s # verify it is OK, should have same numbers of real, upper and lower as # measured in the caeRem3.2bit, only N's are different: faSize super.fa # 145442736 bases (7036533 N's 138406203 real 96215522 upper # 42190681 lower) in 3670 sequences in 1 files # %29.01 masked total, %30.48 masked real # in fact, the missing N's should be: # (3670 - 1) * 1000 = 149111736 - 145442736 = 10705533 - 7036533 = # 3669000 faToTwoBit super.fa caeRem3.supercontigs.2bit twoBitInfo caeRem3.supercontigs.2bit stdout | sort -k2nr \ > caeRem3.supercontigs.sizes # Copy this 2bit file and sizes over to /san/sanvol1/scratch/worms/caeRem3 # the lft2BitToFa.pl script is: cat << '_EOF_' #!/usr/bin/env perl use strict; use warnings; use File::Basename; sub usage() { printf "usage: %s [more_files.lft]\n", basename($0); printf "\tfasta output is to stdout, therefore route stdout to result file\n"; exit 255; } my $argc = scalar(@ARGV); usage if ($argc < 2); my $twoBitFile = shift; while (my $liftFile = shift) { open (FH,"<$liftFile") or die "Can not open $liftFile"; while (my $line=) { chomp $line; my ($start, $contig, $length, $chrom, $chrom_length) = split('\s',$line); my $cmd=sprintf("twoBitToFa $twoBitFile:%s:%d-%d stdout", $chrom, $start, $start+$length); print `$cmd | sed -e "s#^>.*#>$contig#"`; } close (FH); } '_EOF_' # << happy emacs ######################################################################### # MAKE 11.OOC FILE FOR BLAT/GENBANK (DONE - 2008-05-23 - Hiram) # Use -repMatch=50 (based on size -- for human we use 1024, and # C. remanei size is ~5.1% of human judging by gapless caeRem2 vs. hg18 # genome sizes from featureBits. So we would use 50, but that yields a very # high number of tiles to ignore, especially for a small more compact # genome. Bump that up a bit to be more conservative. # This more conservative setting was done June 4th. ssh kkstore01 cd /cluster/data/caeRem3 blat caeRem3.2bit /dev/null /dev/null -tileSize=11 \ -makeOoc=jkStuff/11.ooc -repMatch=100 # Wrote 10173 overused 11-mers to 11.ooc cp -p jkStuff/11.ooc /san/sanvol1/scratch/worms/caeRem3 # the san directory should have: # -rw-rw-r-- 1 16 May 13 09:52 chrom.sizes # -rw-rw-r-- 1 59427484 May 13 11:21 caePb2.2bit # -rw-rw-r-- 1 58631157 May 13 11:31 caePb2.supercontigs.2bit # -rw-rw-r-- 1 56860 May 13 11:31 caePb2.supercontigs.sizes # -rw-rw-r-- 1 40700 Jun 4 11:42 11.ooc # copy those files to /cluster/bluearc/scratch/data/caeRem3/ # and to the Iservers /iscratch/i/worms/caeRem3/ # request an rsync of /scratch/data/ from the cluster admins ######################################################################### # GENBANK AUTO UPDATE (DONE - 2008-05-23 - Hiram) # align with latest genbank process. ssh hgwdev cd ~/kent/src/hg/makeDb/genbank cvsup # edit etc/genbank.conf to add caePb2 just before caeRem2 # caeRem3 (C. remanei) caeRem3.serverGenome = /cluster/data/caeRem3/caeRem3.2bit caeRem3.clusterGenome = /iscratch/i/worms/caeRem3/caeRem3.2bit caeRem3.ooc = /iscratch/i/worms/caeRem3/11.ooc caeRem3.lift = /iscratch/i/worms/caeRem3/caeRem3.chrUn.lift caeRem3.align.unplacedChroms = chrUn caeRem3.refseq.mrna.native.pslCDnaFilter = ${lowCover.refseq.mrna.native.pslCDnaFilter} caeRem3.refseq.mrna.xeno.pslCDnaFilter = ${lowCover.refseq.mrna.xeno.pslCDnaFilter} caeRem3.genbank.mrna.native.pslCDnaFilter = ${lowCover.genbank.mrna.native.pslCDnaFilter} caeRem3.genbank.mrna.xeno.pslCDnaFilter = ${lowCover.genbank.mrna.xeno.pslCDnaFilter} caeRem3.genbank.est.native.pslCDnaFilter = ${lowCover.genbank.est.native.pslCDnaFilter} caeRem3.refseq.mrna.native.load = no caeRem3.refseq.mrna.xeno.load = yes caeRem3.refseq.mrna.xeno.loadDesc = yes caeRem3.genbank.mrna.xeno.load = yes caeRem3.genbank.est.native.load = yes caeRem3.genbank.est.native.loadDesc = no caeRem3.downloadDir = caeRem3 caeRem3.perChromTables = no cvs ci -m "Added caeRem3." etc/genbank.conf # update /cluster/data/genbank/: make etc-update ssh genbank cd /cluster/data/genbank time nice -n +19 bin/gbAlignStep -initial caeRem3 & # var/build/logs/2008.05.23-10:34:13.caeRem3.initalign.log # real 133m52.226s # load database when finished ssh hgwdev cd /cluster/data/genbank time nice -n +19 ./bin/gbDbLoadStep -drop -initialLoad caeRem3 # logFile: var/dbload/hgwdev/logs/2008.05.23-14:22:08.dbload.log # real 17m45.023s # enable daily alignment and update of hgwdev cd ~/kent/src/hg/makeDb/genbank cvsup # add caeRem3 to: etc/align.dbs etc/hgwdev.dbs cvs ci -m "Added caeRem3 - C. remanei" etc/align.dbs etc/hgwdev.dbs make etc-update ############################################################################ # BLATSERVERS ENTRY (DONE - 2008-05-23 - Hiram) # After getting a blat server assigned by the Blat Server Gods, ssh hgwdev hgsql -e 'INSERT INTO blatServers (db, host, port, isTrans, canPcr) \ VALUES ("caeRem3", "blat11", "17788", "1", "0"); \ INSERT INTO blatServers (db, host, port, isTrans, canPcr) \ VALUES ("caeRem3", "blat11", "17789", "0", "1");' \ hgcentraltest # test it with some sequence ############################################################################ ## Default position (DONE - 2008-05-23 - Hiram) ssh hgwdev hgsql -e 'update dbDb set defaultPos="chrUn:119043304-119068959" where name="caeRem3";' hgcentraltest ########################################################################## ## Creating downloads (DONE - 2008-05-23 - Hiram) # There is only one chrom, make its trfMaskChrom file exist ssh hgwdev mkdir /cluster/data/caeRem3/bed/simpleRepeat/trfMaskChrom cd /cluster/data/caeRem3/bed/simpleRepeat/trfMaskChrom ## symlink didn't work here, the symlink ended up in the tar file cp -p ../trfMask.bed ./chrUn.bed cd /cluster/data/caeRem3 # there is no RM file time nice -n +19 /cluster/bin/scripts/makeDownloads.pl caeRem3 # real 2m10.175s ## *!* EDIT THE README.txt FILES *!* in goldenPath/*/README.txt ## cp -p bed/windowMasker/cleanWMask.bed.gz \ goldenPath/bigZips/chromWMSdust.bed.gz ########################################################################## ## Creating pushQ (DONE - 2008-05-23 - Hiram) ssh hgwdev mkdir /cluster/data/caeRem3/pushQ cd /cluster/data/caeRem3/pushQ /cluster/bin/scripts/makePushQSql.pl caeRem3 > caeRem3.sql 2> stderr.out ########################################################################## # Fixup assembly date after confirmation from John Spieth # 2008-05-27 - DONE - Hiram ssh hgwdev hgsql -e 'update dbDb set description="May 2007" where name="caeRem3"' \ hgcentraltest ######################################################################### # ELEGANS (ce6) PROTEINS TRACK (DONE - Hiram - 2008-06-11) ssh kkstore01 # breaking up this target genome into manageable pieces # using the contigs so we don't have genes spanning non-bridged gaps mkdir /cluster/data/caeRem3/blastDb cd /cluster/data/caeRem3 twoBitToFa -noMask maskedContigs/caeRem3.supercontigs.2bit temp.fa faSplit gap temp.fa 1000000 blastDb/x -lift=blastDb.lft # 3709 pieces of 3709 written rm temp.fa cd blastDb for i in *.fa do /cluster/bluearc/blast229/formatdb -i $i -p F done rm *.fa ## copy to san for kluster access mkdir -p /san/sanvol1/scratch/worms/caeRem3/blastDb cd /san/sanvol1/scratch/worms/caeRem3/blastDb rsync -a --progress --stats /cluster/data/caeRem3/blastDb/ . ## create the query protein set mkdir -p /cluster/data/caeRem3/bed/tblastn.ce6SG cd /cluster/data/caeRem3/bed/tblastn.ce6SG echo /san/sanvol1/scratch/worms/caeRem3/blastDb/*.nsq | xargs ls -S \ | sed "s/\.nsq//" > query.lst wc -l query.lst # 3709 query.lst # we want around 100000 jobs calc `wc /cluster/data/ce6/bed/blat.ce6SG/ce6SG.psl | awk "{print \\\$1}"`/\(100000/`wc query.lst | awk "{print \\\$1}"`\) # 23741/(100000/3709) = 880.553690 mkdir -p /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/sgfa split -l 880 /cluster/data/ce6/bed/blat.ce6SG/ce6SG.psl \ /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/sgfa/sg ln -s /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/sgfa sgfa cd sgfa for i in *; do nice pslxToFa $i $i.fa; rm $i; done cd .. ls -1S sgfa/*.fa > sg.lst mkdir -p /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/blastOut ln -s /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/blastOut for i in `cat sg.lst`; do mkdir blastOut/`basename $i .fa`; done cd /cluster/data/caeRem3/bed/tblastn.ce6SG cat << '_EOF_' > template #LOOP blastSome $(path1) {check in line $(path2)} {check out exists blastOut/$(root2)/q.$(root1).psl } #ENDLOOP '_EOF_' # << happy emacs cat << '_EOF_' > blastSome #!/bin/sh CBIN=/cluster/bin/i386 DB=caeRem3 BLASTMAT=/scratch/data/blast229/data SCR="/scratch/tmp/${DB}" g=`/bin/basename $2` D=`/bin/basename $1` R=`/bin/basename $3` inputFile=${SCR}/${D}_${g} export CBIN DB BLASTMAT SCR g D R /bin/mkdir -p ${SCR} /bin/cp -p $1.* ${SCR} /bin/cp -p $2 ${inputFile} /bin/cp -p /cluster/store10/${DB}/blastDb.lft ${SCR}/${D}_blastDb.lft /bin/cp -p /cluster/store3/worm/ce6/bed/blat.ce6SG/protein.lft \ ${SCR}/${D}_protein.lft f=${SCR}/${R}.$g for eVal in 0.01 0.001 0.0001 0.00001 0.000001 1E-09 1E-11 do if /scratch/data/blast229/blastall -M BLOSUM80 -m 0 -F no \ -e $eVal -p tblastn -d ${SCR}/${D} -i ${inputFile} -o $f.8 then /bin/mv $f.8 $f.1 break; fi done if test -f $f.1 then if ${CBIN}/blastToPsl $f.1 $f.2 then ${CBIN}/liftUp -nosort -type=".psl" -nohead $f.3 \ ${SCR}/${D}_blastDb.lft carry $f.2 > /dev/null ${CBIN}/liftUp -nosort -type=".psl" -pslQ -nohead ${SCR}/${R}.tmp \ ${SCR}/${D}_protein.lft warn $f.3 > /dev/null if ${CBIN}/pslCheck -prot ${SCR}/${R}.tmp then /bin/rm -f $3 /bin/mv ${SCR}/${R}.tmp $3 /bin/rm -f $f.1 $f.2 $f.3 $f.4 ${SCR}/${D}.* ${inputFile} \ ${SCR}/${D}_protein.lft ${SCR}/${D}_blastDb.lft /bin/rmdir --ignore-fail-on-non-empty ${SCR} fi exit 0 fi fi /bin/rm -f $f.1 $f.2 $3.tmp $f.8 $f.3 $f.4 ${SCR}/${D}.* ${inputFile} \ ${SCR}/${D}_protein.lft ${SCR}/${D}_blastDb.lft /bin/rmdir --ignore-fail-on-non-empty ${SCR} exit 1 '_EOF_' # << happy emacs chmod +x blastSome ssh kk cd /cluster/data/caeRem3/bed/tblastn.ce6SG gensub2 query.lst sg.lst template jobList para create jobList # para try, check, push, check etc. # Completed: 100142 of 100143 jobs # Other count: 1 jobs # CPU time in finished jobs: 9711211s 161853.51m 2697.56h 112.40d 0.308 y # IO & Wait Time: 1135276s 18921.27m 315.35h 13.14d 0.036 y # Average job time: 108s 1.81m 0.03h 0.00d # Longest finished job: 706s 11.77m 0.20h 0.01d # Submission to last job: 32977s 549.62m 9.16h 0.38d # the 1 stray job was a tracking error. It did get finished, # there was a result file and para recover said nothing was left to do # do the cluster run for chaining ssh kk mkdir /cluster/data/caeRem3/bed/tblastn.ce6SG/chainRun cd /cluster/data/caeRem3/bed/tblastn.ce6SG/chainRun cat << '_EOF_' > template #LOOP chainOne $(path1) #ENDLOOP '_EOF_' # << happy emacs cat << '_EOF_' > chainOne (cd $1; cat q.*.psl | simpleChain -prot -outPsl -maxGap=50000 stdin /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/blastOut/c.`basename $1`.psl) '_EOF_' # << happy emacs chmod +x chainOne ls -1dS /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG/blastOut/sg?? \ > chain.lst gensub2 chain.lst single template jobList cd /cluster/data/caeRem3/bed/tblastn.ce6SG/chainRun para create jobList # para maxNode 30 # there are only 27 jobs para try, check, push, check etc. # Completed: 27 of 27 jobs # CPU time in finished jobs: 394s 6.57m 0.11h 0.00d 0.000 y # IO & Wait Time: 2095s 34.91m 0.58h 0.02d 0.000 y # Average job time: 92s 1.54m 0.03h 0.00d # Longest finished job: 110s 1.83m 0.03h 0.00d # Submission to last job: 183s 3.05m 0.05h 0.00d ssh kkstore01 cd /cluster/data/caeRem3/bed/tblastn.ce6SG/blastOut for i in sg?? do cat c.$i.psl | awk "(\$13 - \$12)/\$11 > 0.6 {print}" > c60.$i.psl sort -rn c60.$i.psl | pslUniq stdin u.$i.psl awk "((\$1 / \$11) ) > 0.60 { print }" c60.$i.psl > m60.$i.psl echo $i done sort -T /scratch/tmp -k 14,14 -k 16,16n -k 17,17n u.*.psl m60* | uniq \ > /cluster/data/caeRem3/bed/tblastn.ce6SG/blastCe6SG.psl cd .. pslCheck blastCe6SG.psl # checked: 29004 failed: 0 errors: 0 # load table ssh hgwdev cd /cluster/data/caeRem3/bed/tblastn.ce6SG liftUp -nohead -type=.psl stdout ../../downloads/caeRem3.chrUn.lift \ error blastCe6SG.psl | sort -k14,14 -k16,16n \ | hgLoadPsl -table=blastCe6SG caeRem3 stdin # check coverage featureBits caeRem3 blastCe6SG # 20355944 bases of 138406388 (14.707%) in intersection featureBits caeRem2 blastCe4SG # 19763359 bases of 146898439 (13.454%) in intersection featureBits ce6 sangerGene # 28134889 bases of 100281426 (28.056%) in intersection ssh kkstore01 rm -rf /cluster/data/caeRem3/bed/tblastn.ce6SG/blastOut rm -rf /cluster/bluearc/worms/caeRem3/bed/tblastn.ce6SG ########################################################################### # ELEGANS (ce9) PROTEINS TRACK (DONE - 2010-10-07 - Hiram) cd /hive/data/genomes/caeRem3 mv blastDb blastDb.2008-06-17 mv blastDb.lft blastDb.lft.2008-06-17 mkdir blastDb twoBitToFa caeRem3.unmasked.2bit temp.fa faSplit gap temp.fa 1000000 blastDb/x -lift=blastDb.lft # 177 pieces of 177 written rm temp.fa cd blastDb for i in *.fa do /scratch/data/blast-2.2.11/bin/formatdb -i $i -p F done rm *.fa ## create the query protein set mkdir -p /hive/data/genomes/caeRem3/bed/tblastn.ce9SG cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG echo /hive/data/genomes/caeRem3/blastDb/*.nsq | xargs ls -S \ | sed "s/\.nsq//" > query.lst wc -l query.lst # 9538 query.lst # we want around 50000 jobs calc `wc -l /hive/data/genomes/ce9/bed/blat.ce9SG/ce9SG.psl | cut -d" " -f1`/\(50000/`wc -l query.lst | cut -d" " -f1`\) # 28103/(50000/177) = 99.484620 mkdir sgfa split -l 90 /hive/data/genomes/ce9/bed/blat.ce9SG/ce9SG.psl sgfa/sg cd sgfa for i in *; do nice pslxToFa $i $i.fa; rm $i; done cd .. ls -1S sgfa/*.fa > sg.lst mkdir blastOut for i in `cat sg.lst`; do mkdir blastOut/`basename $i .fa`; done cat << '_EOF_' > template #LOOP blastSome $(path1) {check in line $(path2)} {check out exists blastOut/$(root2)/q.$(root1).psl } #ENDLOOP '_EOF_' # << happy emacs cat << '_EOF_' > blastSome #!/bin/sh DB=caeRem3 BLASTMAT=/scratch/data/blast-2.2.11/data SCR="/scratch/tmp/${DB}" g=`basename $2` D=`basename $1` export BLASTMAT DB SCR g D mkdir -p ${SCR} cp -p $1.* ${SCR} f=${SCR}/`basename $3`.$g for eVal in 0.01 0.001 0.0001 0.00001 0.000001 1E-09 1E-11 do if /scratch/data/blast-2.2.11/bin/blastall -M BLOSUM80 -m 0 -F no \ -e $eVal -p tblastn -d ${SCR}/$D -i $2 -o $f.8 then mv $f.8 $f.1 break; fi done if test -f $f.1 then if /cluster/bin/x86_64/blastToPsl $f.1 $f.2 then liftUp -nosort -type=".psl" -nohead $f.3 \ /hive/data/genomes/${DB}/blastDb.lft carry $f.2 > /dev/null liftUp -nosort -type=".psl" -pslQ -nohead $3.tmp \ /hive/data/genomes/ce9/bed/blat.ce9SG/protein.lft warn $f.3 > /dev/null if pslCheck -prot $3.tmp then mv $3.tmp $3 rm -f $f.1 $f.2 $f.3 $f.4 ${SCR}/$D.* rmdir --ignore-fail-on-non-empty ${SCR} fi exit 0 fi fi rm -f $f.1 $f.2 $3.tmp $f.8 $f.3 $f.4 ${SCR}/$D.* rmdir --ignore-fail-on-non-empty ${SCR} exit 1 '_EOF_' # << happy emacs chmod +x blastSome ssh swarm cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG gensub2 query.lst sg.lst template jobList para create jobList para try, check, push, check etc. # Completed: 55401 of 55401 jobs # CPU time in finished jobs: 449440s 7490.67m 124.84h 5.20d 0.014 y # IO & Wait Time: 171423s 2857.05m 47.62h 1.98d 0.005 y # Average job time: 11s 0.19m 0.00h 0.00d # Longest finished job: 28s 0.47m 0.01h 0.00d # Submission to last job: 1997s 33.28m 0.55h 0.02d # do the cluster run for chaining ssh swarm mkdir /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/chainRun cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/chainRun cat << '_EOF_' > template #LOOP chainOne $(path1) {check out exists+ ../blastOut/c.$(file1).psl} #ENDLOOP '_EOF_' # << happy emacs cat << '_EOF_' > chainOne #!/bin/csh -fe cd $1 set b = $1:t cat q.*.psl | simpleChain -prot -outPsl -maxGap=50000 stdin \ /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/blastOut/c.$b.psl '_EOF_' # << happy emacs chmod +x chainOne ls -1dS /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/blastOut/sg?? \ > chain.lst gensub2 chain.lst single template jobList cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/chainRun para create jobList para -maxJob=30 push para try, check, push, check etc. # Completed: 313 of 313 jobs # CPU time in finished jobs: 3546s 59.10m 0.99h 0.04d 0.000 y # IO & Wait Time: 10163s 169.38m 2.82h 0.12d 0.000 y # Average job time: 44s 0.73m 0.01h 0.00d # Longest finished job: 394s 6.57m 0.11h 0.00d # Submission to last job: 461s 7.68m 0.13h 0.01d XXX - ready cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG/blastOut for i in sg?? do cat c.$i.psl | awk "(\$13 - \$12)/\$11 > 0.6 {print}" > c60.$i.psl sort -rn c60.$i.psl | pslUniq stdin u.$i.psl awk "((\$1 / \$11) ) > 0.60 { print }" c60.$i.psl > m60.$i.psl echo $i done sort -T /scratch/tmp -k 14,14 -k 16,16n -k 17,17n u.*.psl m60* | uniq \ > ../blastCe9SG.psl cd .. pslCheck blastCe9SG.psl # checked: 33684 failed: 0 errors: 0 # load table ssh hgwdev cd /hive/data/genomes/caeRem3/bed/tblastn.ce9SG hgLoadPsl caeRem3 blastCe9SG.psl # check coverage featureBits caeRem3 blastCe9SG # 20302540 bases of 138406388 (14.669%) in intersection featureBits cb3 blastCe9SG # 18490367 bases of 108433446 (17.052%) in intersection featureBits caePb2 blastCe9SG # 23730009 bases of 170473138 (13.920%) in intersection featureBits caeJap3 blastCe9SG # 12894398 bases of 154057934 (8.370%) in intersection featureBits melHap1 blastCe9SG # 4376245 bases of 53017507 (8.254%) in intersection featureBits melInc1 blastCe9SG # 3882043 bases of 82095019 (4.729%) in intersection featureBits bruMal1 blastCe9SG # 4424694 bases of 89235536 (4.958%) in intersection featureBits priPac2 blastCe9SG # 5436779 bases of 133634773 (4.068%) in intersection featureBits haeCon1 blastCe9SG # 4990746 bases of 278844984 (1.790%) in intersection featureBits ce9 sangerGene # 28689552 bases of 100286004 (28.608%) in intersection rm -rf blastOut #########################################################################