Dear Bastein, Log file is attached. Thank you, Praveen ______________________________________ From: mira_talk-bounce@xxxxxxxxxxxxx [mira_talk-bounce@xxxxxxxxxxxxx] On Behalf Of Bastien Chevreux [bach@xxxxxxxxxxxx] Sent: Friday, August 06, 2010 5:30 PM To: mira_talk@xxxxxxxxxxxxx Subject: [mira_talk] Re: Help Can you please send the whole log? ----- original Nachricht -------- Betreff: [mira_talk] Re: Help Gesendet: Fr, 06. Aug 2010 Von: Raj Kumar, Praveen Kumar Mr.<rajkump@xxxxxxxxxx> > Dear Bastein, > I am sorry to let you know this, I still the error msg. > > > CMD:/software/mira/mira_3.2.0rc3_dev_linux-gnu_x86_64_static/bin/mira > --project=EAch --job=est,denovo,accurate,sanger,454 SANGER_SETTINGS > -CL:qc=no 454_SETTINGS -LR:mxti=no -AL:mrs=95 -CO:rodirs=5 COMMON_SETTINGS > -SK:mnr=yes:nrr=10 -MI:sonfs=false >& log_assembly.txt > > **************************************************************************** > ***************** > WARNING WARNING WARNING! > > It looks like the log directory is on a NFS mount. This will slow down MIRA > *considerably* ... by about a factor of 10! > If you don't want that, you have three possibilities: > > 1) RECOMMENDED! Use -DI:lrt to redirect the log directory somewhere else on > a > local disk or even SSD. > 2) POSSIBLE: put the whole project somewhere else and restart MIRA. > 3) ABSOLUTELY NOT RECOMMENDED AT ALL: use -MI:sonfs=false to tell MIRA not > to stop when it finds the log directory on NFS. > > > Fatal error (may be due to problems of the input data or parameters): > > "Log directory is on a NFS mount ... but we don't want that." > > ->Thrown: void Assembly::checkForNFSMountOnLogDir() > ->Caught: main > > Aborting process, probably due to error in the input data or > parametrisation. > Please check the output log for more information. > For help, please write a mail to the mira talk mailing list. > > CWD: /shared/liangcres/cdna3055.assembly > Thank you for noticing that this is *NOT* a crash, but a > controlled program stop. > ************************************************************* > > regards, > Praveen > ________________________________________ > From: mira_talk-bounce@xxxxxxxxxxxxx [mira_talk-bounce@xxxxxxxxxxxxx] On > Behalf Of Bastien Chevreux [bach@xxxxxxxxxxxx] > Sent: Friday, August 06, 2010 1:31 PM > To: mira_talk@xxxxxxxxxxxxx > Subject: [mira_talk] Re: Help > > On Donnerstag 05 August 2010 Raj Kumar, Praveen Kumar Mr. wrote: > > Dear Bob, > > I followed suggestion #3 and I still get the following error msg, > > Yikes. I really need some vacation ... failing to implement such an easy > parameter is not a good sign. > > Anyway. > > Praveen, there's a 64 bit hot-fix binary here which should fix your > problem: > > http://www.chevreux.org/tmp/mira.bz2 > > Please tell if it does. > > B. > > > -- > You have received this mail because you are subscribed to the mira_talk > mailing list. For information on how to subscribe or unsubscribe, please > visit http://www.chevreux.org/mira_mailinglists.html > > -- > You have received this mail because you are subscribed to the mira_talk > mailing list. For information on how to subscribe or unsubscribe, please > visit http://www.chevreux.org/mira_mailinglists.html > --- original Nachricht Ende ---- -- You have received this mail because you are subscribed to the mira_talk mailing list. For information on how to subscribe or unsubscribe, please visit http://www.chevreux.org/mira_mailinglists.html
This is MIRA V3.2.0rc3 (development version). Please cite: Chevreux, B., Wetter, T. and Suhai, S. (1999), Genome Sequence Assembly Using Trace Signals and Additional Sequence Information. Computer Science and Biology: Proceedings of the German Conference on Bioinformatics (GCB) 99, pp. 45-56. To (un-)subscribe the MIRA mailing lists, see: http://www.chevreux.org/mira_mailinglists.html After subscribing, mail general questions to the MIRA talk mailing list: mira_talk@xxxxxxxxxxxxx To report bugs or ask for features, please use the new ticketing system at: http://sourceforge.net/apps/trac/mira-assembler/ This ensures that requests don't get lost. Compiled by: bach Sat Jul 31 14:54:28 CEST 2010 On: Linux arcadia64 2.6.27-11-generic #1 SMP Wed Apr 1 20:53:41 UTC 2009 x86_64 GNU/Linux Compiled in boundtracking mode. Compiled in bugtracking mode. Compilation settings (sorry, for debug): Size of size_t : 8 Size of uint32 : 4 Size of uint32_t: 4 Size of uint64 : 8 Size of uint64_t: 8 Current system: Linux compute-0-0.local 2.6.18-164.15.1.el5 #1 SMP Wed Mar 17 11:30:06 EDT 2010 x86_64 x86_64 x86_64 GNU/Linux Parsing parameters: --project=EAch --job=est,denovo,accurate,sanger,454 SANGER_SETTINGS -CL:qc=no 454_SETTINGS -LR:mxti=no -AL:mrs=95 -CO:rodirs=5 COMMON_SETTINGS -SK:mnr=yes:nrr=10 -MI:sonfs=false Parameters parsed without error, perfect. ------------------------------------------------------------------------------ Parameter settings seen for: Sanger data (also common parameters), 454 data Used parameter settings: General (-GE): Project name in (proin) : EAch Project name out (proout) : EAch Number of threads (not) : 2 Automatic memory management (amm) : yes Keep percent memory free (kpmf) : 15 Max. process size (mps) : 0 Keep contigs in memory (kcim) : no EST SNP pipeline step (esps) : 0 Use template information (uti) : [san] yes [454] yes Template insert size minimum (tismin) : [san] -1 [454] -1 Template insert size maximum (tismax) : [san] -1 [454] -1 Template partner build direction (tpbd) : [san] -1 [454] -1 Colour reads by hash frequency (crhf) : no Load reads options (-LR): Load sequence data (lsd) : [san] yes [454] yes File type (ft) : [san] fasta [454] fasta External quality (eq) : from SCF (scf) Ext. qual. override (eqo) : no Discard reads on e.q. error (droeqe): no Solexa scores in qual file (ssiqf) : no FASTQ qual offset (fqqo) : [san] 0 [454] 0 Wants quality file (wqf) : [san] yes [454] yes Read naming scheme (rns) : [san] Sanger Institute (sanger) [454] forward/reverse (fr) Merge with XML trace info (mxti) : [san] no [454] no Filecheck only (fo) : no Assembly options (-AS): Number of passes (nop) : 5 Skim each pass (sep) : yes Maximum number of RMB break loops (rbl) : 3 Minimum read length (mrl) : [san] 80 [454] 40 Minimum reads per contig (mrpc) : [san] 2 [454] 2 Base default quality (bdq) : [san] 10 [454] 10 Enforce presence of qualities (epoq) : [san] yes [454] yes Automatic repeat detection (ard) : no Coverage threshold (ardct) : [san] 2 [454] 2 Minimum length (ardml) : [san] 400 [454] 200 Grace length (ardgl) : [san] 40 [454] 20 Use uniform read distribution (urd) : no Start in pass (urdsip) : 4 Cutoff multiplier (urdcm) : [san] 1.5 [454] 1.5 Keep long repeats separated (klrs) : no Spoiler detection (sd) : no Last pass only (sdlpo) : yes Use genomic pathfinder (ugpf) : no Use emergency search stop (uess) : yes ESS partner depth (esspd) : 500 Use emergency blacklist (uebl) : yes Use max. contig build time (umcbt) : yes Build time in seconds (bts) : 3600 Strain and backbone options (-SB): Load straindata (lsd) : no Load backbone (lb) : no Start backbone usage in pass (sbuip) : 3 Backbone file type (bft) : fasta Backbone base quality (bbq) : 30 Backbone strain name (bsn) : Force for all (bsnffa) : no Backbone rail from strain (brfs) : Backbone rail length (brl) : 0 Backbone rail overlap (bro) : 0 Also build new contigs (abnc) : yes Dataprocessing options (-DP): Use read extensions (ure) : [san] no [454] no Read extension window length (rewl) : [san] 30 [454] 15 Read extension w. maxerrors (rewme) : [san] 2 [454] 2 First extension in pass (feip) : [san] 0 [454] 0 Last extension in pass (leip) : [san] 0 [454] 0 Clipping options (-CL): Merge with SSAHA vector screen (msvs) : [san] no [454] no Gap size (msvsgs) : [san] 10 [454] 8 Max front gap (msvsmfg) : [san] 60 [454] 8 Max end gap (msvsmeg) : [san] 120 [454] 12 Strict front clip (msvssfc) : [san] 0 [454] 0 Strict end clip (msvssec) : [san] 0 [454] 0 Possible vector leftover clip (pvlc) : [san] no [454] no maximum len allowed (pvcmla) : [san] 18 [454] 18 Quality clip (qc) : [san] no [454] no Minimum quality (qcmq) : [san] 20 [454] 20 Window length (qcwl) : [san] 30 [454] 30 Bad stretch quality clip (bsqc) : [san] no [454] no Minimum quality (bsqcmq) : [san] 20 [454] 5 Window length (bsqcwl) : [san] 30 [454] 20 Masked bases clip (mbc) : [san] yes [454] yes Gap size (mbcgs) : [san] 20 [454] 5 Max front gap (mbcmfg) : [san] 40 [454] 12 Max end gap (mbcmeg) : [san] 60 [454] 12 Lower case clip (lcc) : [san] no [454] yes Clip poly A/T at ends (cpat) : [san] yes [454] yes Keep poly-a signal (cpkps) : [san] no [454] no Minimum signal length (cpmsl) : [san] 12 [454] 12 Max errors allowed (cpmea) : [san] 1 [454] 1 Max gap from ends (cpmgfe) : [san] 20000 [454] 20000 Ensure minimum left clip (emlc) : [san] no [454] no Minimum left clip req. (mlcr) : [san] 25 [454] 4 Set minimum left clip to (smlc) : [san] 30 [454] 4 Ensure minimum right clip (emrc) : [san] no [454] no Minimum right clip req. (mrcr) : [san] 10 [454] 10 Set minimum right clip to (smrc) : [san] 20 [454] 15 Apply SKIM chimera detection clip (ascdc) : no Apply SKIM junk detection clip (asjdc) : no Propose end clips (pec) : no Bases per hash (pecbph) : 17 Handle Solexa GGCxG problem (pechsgp) : yes Parameters for SKIM algorithm (-SK): Number of threads (not) : 2 Also compute reverse complements (acrc) : yes Bases per hash (bph) : 21 Hash save stepping (hss) : 1 Percent required (pr) : [san] 70 [454] 80 Max hits per read (mhpr) : 30 Max megahub ratio (mmhr) : 0 Freq. est. min normal (fenn) : 0.4 Freq. est. max normal (fexn) : 1.6 Freq. est. repeat (fer) : 1.9 Freq. est. heavy repeat (fehr) : 8 Freq. est. crazy (fecr) : 20 Mask nasty repeats (mnr) : yes Nasty repeat ratio (nrr) : 10 Repeat level in info file (rliif) : 6 Max hashes in memory (mhim) : 15000000 MemCap: hit reduction (mchr) : 2048 Pathfinder options (-PF): Use quick rule (uqr) : [san] yes [454] yes Quick rule min len 1 (qrml1) : [san] 200 [454] 80 Quick rule min sim 1 (qrms1) : [san] 90 [454] 90 Quick rule min len 2 (qrml2) : [san] 100 [454] 60 Quick rule min sim 2 (qrms2) : [san] 95 [454] 95 Backbone quick overlap min len (bqoml) : [san] 150 [454] 80 Align parameters for Smith-Waterman align (-AL): Bandwidth in percent (bip) : [san] 20 [454] 20 Bandwidth max (bmax) : [san] 130 [454] 80 Bandwidth min (bmin) : [san] 25 [454] 20 Minimum score (ms) : [san] 30 [454] 15 Minimum overlap (mo) : [san] 15 [454] 20 Minimum relative score in % (mrs) : [san] 85 [454] 95 Solexa_hack_max_errors (shme) : [san] 0 [454] 0 Extra gap penalty (egp) : [san] yes [454] yes extra gap penalty level (egpl) : [san] reject_codongaps [454] reject_codongaps Max. egp in percent (megpp) : [san] 100 [454] 100 Contig parameters (-CO): Name prefix (np) : EAch Reject on drop in relative alignment score in % (rodirs) : [san] 10 [454] 5 Mark repeats (mr) : yes Only in result (mroir) : no Assume SNP instead of repeats (asir) : no Minimum reads per group needed for tagging (mrpg) : [san] 2 [454] 4 Minimum neighbour quality needed for tagging (mnq) : [san] 20 [454] 20 Minimum Group Quality needed for RMB Tagging (mgqrt) : [san] 30 [454] 25 End-read Marking Exclusion Area in bases (emea) : [san] 25 [454] 10 Set to 1 on clipping PEC (emeas1clpec) : yes Also mark gap bases (amgb) : [san] yes [454] no Also mark gap bases - even multicolumn (amgbemc) : [san] yes [454] yes Also mark gap bases - need both strands (amgbnbs): [san] yes [454] yes Force non-IUPAC consensus per sequencing type (fnicpst) : [san] no [454] no Merge short reads (msr) : [san] no [454] no Gap override ratio (gor) : [san] 66 [454] 66 Edit options (-ED): Automatic contig editing (ace) : [san] no [454] yes Sanger only: Strict editing mode (sem) : no Confirmation threshold in percent (ct) : 50 Misc (-MI): Stop on NFS (sonfs) : yes Directories (-DI): When loading EXP files : When loading SCF files : Top directory for writing files : EAch_assembly For writing result files : EAch_assembly/EAch_d_results For writing result info files : EAch_assembly/EAch_d_info For writing log files : EAch_assembly/EAch_d_log Log redirected to (lrt) : For writing checkpoint files : EAch_assembly/EAch_d_chkpt File names (-FN): When loading sequences from FASTA : [san] EAch_in.sanger.fasta [454] EAch_in.454.fasta When loading qualities from FASTA quality : [san] EAch_in.sanger.fasta.qual [454] EAch_in.454.fasta.qual When loading sequences from FASTQ : [san] EAch_in.sanger.fastq [454] EAch_in.454.fastq When loading project from CAF : EAch_in.sanger.caf When loading project from MAF (disabled) : EAch_in.sanger.maf When loading EXP fofn : EAch_in.sanger.fofn When loading project from PHD : EAch_in.phd.1 When loading strain data : EAch_straindata_in.txt When loading XML trace info files : [san] EAch_traceinfo_in.sanger.xml [454] EAch_traceinfo_in.454.xml When loading SSAHA vector screen results : EAch_ssaha2vectorscreen_in.txt When loading backbone from MAF : EAch_backbone_in.maf When loading backbone from CAF : EAch_backbone_in.caf When loading backbone from GenBank : EAch_backbone_in.gbf When loading backbone from FASTA : EAch_backbone_in.fasta Output files (-OUTPUT/-OUT): Save simple singlets in project (sssip) : [san] no [454] no Save tagged singlets in project (stsip) : [san] yes [454] yes Remove rollover logs (rrol) : yes Remove log directory (rld) : no Result files: Saved as CAF (orc) : yes Saved as FASTA (orf) : yes Saved as GAP4 (directed assembly) (org) : no Saved as phrap ACE (ora) : yes Saved as HTML (orh) : no Saved as Transposed Contig Summary (ors) : yes Saved as simple text format (ort) : no Saved as wiggle (orw) : no Temporary result files: Saved as CAF (otc) : yes Saved as MAF (otm) : no Saved as FASTA (otf) : no Saved as GAP4 (directed assembly) (otg) : no Saved as phrap ACE (ota) : no Saved as HTML (oth) : no Saved as Transposed Contig Summary (ots) : no Saved as simple text format (ott) : no Extended temporary result files: Saved as CAF (oetc) : no Saved as FASTA (oetf) : no Saved as GAP4 (directed assembly) (oetg) : no Saved as phrap ACE (oeta) : no Saved as HTML (oeth) : no Save also singlets (oetas) : no Alignment output customisation: TEXT characters per line (tcpl) : 60 HTML characters per line (hcpl) : 60 TEXT end gap fill character (tegfc) : HTML end gap fill character (hegfc) : File / directory output names: CAF : EAch_out.caf MAF : EAch_out.maf FASTA : EAch_out.unpadded.fasta FASTA quality : EAch_out.unpadded.fasta.qual FASTA (padded) : EAch_out.padded.fasta FASTA qual.(pad): EAch_out.padded.fasta.qual GAP4 (directory): EAch_out.gap4da ACE : EAch_out.ace HTML : EAch_out.html Simple text : EAch_out.txt TCS overview : EAch_out.tcs Wiggle : EAch_out.wig ------------------------------------------------------------------------------ Creating directory EAch_assembly ... done. Creating directory EAch_assembly/EAch_d_log ... done. Creating directory EAch_assembly/EAch_d_results ... done. Creating directory EAch_assembly/EAch_d_info ... done. Creating directory EAch_assembly/EAch_d_chkpt ... done. WARNING WARNING WARNING! It looks like the log directory is on a NFS mount. This will slow down MIRA *considerably* ... by about a factor of 10! If you don't want that, you have three possibilities: 1) RECOMMENDED! Use -DI:lrt to redirect the log directory somewhere else on a local disk or even SSD. 2) POSSIBLE: put the whole project somewhere else and restart MIRA. 3) ABSOLUTELY NOT RECOMMENDED AT ALL: use -MI:sonfs=false to tell MIRA not to stop when it finds the log directory on NFS. Fatal error (may be due to problems of the input data or parameters): "Log directory is on a NFS mount ... but we don't want that." ->Thrown: void Assembly::checkForNFSMountOnLogDir() ->Caught: main Aborting process, probably due to error in the input data or parametrisation. Please check the output log for more information. For help, please write a mail to the mira talk mailing list. CWD: /shared/liangcres/cdna3055.assembly Thank you for noticing that this is *NOT* a crash, but a controlled program stop.