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//home/cluster1/data/bu01/1121861/jlex/alignment/clustalw.exe
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H _pH^ËD$PHVW ΉH _P^UC 3ES]3҉EE ;VWEN@ SSvOE}쥥SeS_EPSSOE e e EEPS EMu39Su/{KE ;st{ SE YstMfE3M_^fC [RU0C 3ES] EEVȾ #fWEEEEEEEEEEEE?E tC-C fҋ} u u 9} f;ux ;f u} t @uhZC Fft u } u.h ZC ;u#} u hZC CPCe YYl hYC CPCiM fe NkM EEjPEPfU}7 f}?rEPEPF YYE}f3t C0 ~j_u? fe E EPMYu}ށ ~ EP)NYuOɍCE~PMu}ХEPEPEPEPaEPEMe 0EMuEHH5K|A 89u 0H;s;s@f *,Cd EM3M_^[PÀ80uH;s;s0f# c 3C C@Vt$FP' YuF-t+uF30| 90t AF݃-^uU -C 3ES]V3; D E D ˃ D jVST E jVS< W} +~oh VPڵh S E ;}PPS t+=<D u <D uS YY@}>j u S誌SlPB Nu<D B <D j uSl _ <D M3M^[>NU(C 3ES] E33fK VuEE؉E܉EfF W #3# f=U f f f?w3:fuE3Vu9Fu 9uo 3f;u ESu9Cu9u FFk EE܉EE E} ~IƉEE KMEEM MQP1 tEf EmMuȃEEM } E f} ~%EuEP+E f} Yf} 9E f} }+E]EtEEPKYu} tMf} wE% = u5}u,e }u e f}u EfE fEEEڋEf=sfMfM܉NMN fF ff & ~M3M_^[LUC 3ES C 3Ƀ`9M Et]} ] `C `9MuEf9M t@VWE } T;t&@4f> r }𥥥MuVuUYY39M u_^M3M[zK3UM3AMAMS3ۉA MVCWt E XE tEHE tEHE tEHE tEHE u E3Hj1HE3H_1HE3H1HE3H#1HE3H#1H tMI tMI tMI tM y tE X #t4= t = t ;u(E E E ˉE #t = t ;u"E E EEM3 1E X EH ωH E EXE X`EH` ϋ} H`EXP EPSj uB E@t&@t&@t&@t&Xt&ߋ t1It It Iu*N $ ! tItIu !#ʁ #ʁ @P _^[]UESV3ۋ Cut]tSb Y tEtjH Y E j& EY # = t[= t*; M B C At]EtM B AuC C ]EJM B AuC C ]E M B C At]E E 3tW} B D EPQQ $$M]E } B S B z33EfE;} +]tum]tMmHutE]E _tj YeuEtE t j t Y3^[ËD$t~<D " <D ! Q|$ D$ YQ|$ D$ YUQ}E M#M #E E m EQQL$ t -C \$ t-C \$ t -C \$ t ؛ t\$ YYUW}3كE 8t3_ËL$t I8 t@uID$+Hj@hZC rC 3EE33F9= ?D u2V`B PVPWWB t5 ?D B xu ?D 9}~uE~YEE ;~ PEjYE ?D j[;9 ;1 ;V }}܉}9} u =D M 9}t; 9Eu ; 9u~jX EPu B 9}~+9]rٍEʀ} tЊPtɋM :r:vÀ8 u9} ~>9]= Eʀ} 0 P% M :r:hÀ8 u WWuuj u LB ؉];i }誴eĉEM 3@Ëe e M]3F3E;uPMYE; uSPuuVu LB j j u uj u LB u E 6e}M3@Ëe3M]uu6PMYt@E VWu uju LB tVWSuu uB E} tWLY} t uLYE }9}u|=D E] ;u =D uYu3};tIj j EPuVStj j E PuVSEu WKY븉}EEu uuuu uB tWYKuQKYYƍeM3M!BnV5$=D "WPt$ u <=t tu؋+$=D ^Ë+$=D ^UQ3ɅuÃ? t A8 uS VPkKYuuj _RYP Yu!E^[U S39]VW]tXj=u;YYutC9ut>38FE$=D ;(=D u S$=D ;uU9] t9 ,=D tt?_^[9]2 jJ;Y$=D tމ9 ,=D ujJ;Y,=D tÉ $=D u+VY|?; t:46I39EYuEWNG9uPSvJYYt81} }ߍ PSPJYY@ a 1$=D } tQu訁@@PIYYt9uV+EYEY M@#QVB uMVHY} t uHYEVHY3UQM v^fe W3}f=D E M _u3j5D E5ľD PjE Pjh tf} uEt3@Ã=tC ~ jQ>YYálC HËD$; D Vs[ D T tA3 % 9t$ u |$ @ uɀ% ƈ ^<D <D ^Vt$t V$@PcHYYt VP萹YY^3^%XB T\ d\ |\ \ \ \ \ \ \ \ \ ] ] .] @] P] ^] p] ] ] ] ] ] ] ] ^ "^ 2^ H^ ^^ x^ ^ ^ ^ ^ ^ ^ ^ ^ _ _ 0_ H_ b_ |_ _ _ _ _ _ _ _ _ ` ` 0` F` X` b` n` ~` ` ` ` W> P Z Z Alignment Score %d BError: matrix blosum30 not found None Structure and Penalty Mask Gap Penalty Mask Secondary Structure Unrecognised Command Enter number (or [RETURN] to exit) -- -- Current output is %s H. HELP 4. %s 3. %s 2. %s 1. %s ********* Secondary Structure Output Menu ********* Enter number (or [RETURN] to exit) H. HELP 5. Toggle Phylip bootstrap positions = %s BRANCH LABELS NODE LABELS 4. Toggle Nexus format tree output = %s 3. Toggle Phylip distance matrix output = %s 2. Toggle Phylip format tree output = %s 1. Toggle CLUSTAL format tree output = %s ON OFF ****** Format of Phylogenetic Tree Output ****** Error: signal .. Interrupt Enter number Gap Separation Distance Currently: %d Enter residues (or [RETURN] to quit) Hydrophilic Residues Currently: %s 5. Toggle End Gap Separation :%s 4. Gap Separation Distance :%d 3. Hydrophilic Residues :%s 2. Toggle Hydrophilic Penalties :%s 1. Toggle Residue-Specific Penalties :%s ********* PROTEIN GAP PARAMETERS ********* (file = %s) -- Current matrix is the %s %d. %s ********* %s WEIGHT MATRIX MENU ********* (y/n) ? [y] %s FATAL ERROR: ERROR: WARNING: Enter number of residues outside strand Enter number of residues within strand within strand: %d outside strand: %d Strand Terminal Positions Currently: Enter number of residues outside helix Enter number of residues within helix within helix: %d outside helix: %d Helix Terminal Positions Currently: Secondary Structure Terminal Penalty Currently: %d Loop Gap Penalty Currently: %d Strand Gap Penalty Currently: %d Helix Penalty Currently: %d 9. Strand terminal positions within :%d outside :%d 8. Helix terminal positions within :%d outside :%d 7. Secondary structure terminal penalty :%d 6. Loop gap penalty :%d 5. Strand gap penalty :%d 4. Helix gap penalty :%d = %s 3. Output in alignment 2. Use profile 2 secondary structure / penalty mask = NO = YES 1. Use profile 1 secondary structure / penalty mask ********* SECONDARY STRUCTURE OPTIONS ********* amenu.pim Your choice or press [RETURN] to go back to main menu H. HELP S. Execute a system command 6. Output format options 5. Bootstrap tree 4. Draw tree now 3. Correct for multiple substitutions? = OFF = ON 2. Exclude positions with gaps? 1. Input an alignment ****** PHYLOGENETIC TREE MENU ****** No sequences loaded R. Toggle sequence range numbers = %s T. Toggle parameter output = %s 0. Create alignment output file(s) now? 9. Toggle output order = %s ALIGNED INPUT FILE 8. Toggle CLUSTALW sequence numbers = %s 7. Toggle GDE output case = %s LOWER UPPER 6. Toggle GDE format output = %s 5. Toggle NEXUS format output = %s 4. Toggle PHYLIP format output = %s 3. Toggle GCG/MSF format output = %s 2. Toggle NBRF/PIR format output = %s 1. Toggle CLUSTAL format output = %s F. Toggle FASTA format output = %s ********* Format of Alignment Output ********* Window size Currently: %d Top diagonals Currently: %d K-tuple Currently: %d Gap Penalty Currently: %d DNA PROTEIN Gap Extension Penalty Currently: %4.2f Gap Open Penalty Currently: %4.2f = SLOW = FAST 9. Toggle Slow/Fast pairwise alignments 8. Window size :%d 7. No. of top diagonals :%d 6. K-tuple (word) size :%d 5. Gap penalty :%d Fast/Approximate alignments: 4. DNA weight matrix :%s 3. Protein weight matrix :%s 2. Gap Extension Penalty :%4.2f 1. Gap Open Penalty :%4.2f Slow/Accurate alignments: ********* PAIRWISE ALIGNMENT PARAMETERS ********* Transition Weight Currently: %1.2f Min Identity Currently: %d Gap Opening Penalty Currently: %4.2f 8. Protein Gap Parameters 7. Use negative matrix :%s 6. DNA weight matrix :%s 5. Protein weight matrix :%s 4. DNA Transitions Weight :%1.2f 3. Delay divergent sequences :%d %% 2. Gap Extension Penalty :%4.2f 1. Gap Opening Penalty :%4.2f ********* MULTIPLE ALIGNMENT PARAMETERS ********* 9. Output format options 8. Toggle screen display = %s = OFF = ON 7. Reset gaps before alignment? 6. Multiple alignment parameters 5. Pairwise alignment parameters 4. Toggle Slow/Fast pairwise alignments = %s FAST SLOW 3. Do alignment using old guide tree file 2. Produce guide tree file only 1. Do complete multiple alignment now (%s) Fast/Approximate Slow/Accurate ****** MULTIPLE ALIGNMENT MENU ****** 0. Secondary structure options 8. Toggle screen display = %s 7. Multiple alignment parameters 6. Pairwise alignment parameters 5. Toggle Slow/Fast pairwise alignments = %s 4. Align sequences to 1st. profile (%s) 3. Align 2nd. profile to 1st. profile 2. Input 2nd. profile/sequences (loaded) 1. Input 1st. profile ****** PROFILE AND STRUCTURE ALIGNMENT MENU ****** X. EXIT (leave program) H. HELP S. Execute a system command 4. Phylogenetic trees 3. Profile / Structure Alignments 2. Multiple Alignments 1. Sequence Input From Disc ******** CLUSTAL %s Multiple Sequence Alignments ******** ************************************************************** %d ? ?{Gz? Y@ %d:%d Extension penalties: %d:%d Opening penalties: @gap_pos: gaps: gap open %d gap ext %d Using variable zones to set gap penalties (pcid = %d) A ?Continue SUGGESTION: Remove one or more problem sequences and try again This may not be fatal but you have been warned! (All distances should be between 0.0 and 1.0) %s and %s (distance %1.3f) The following sequences are too divergent to be aligned: ? ? %f tree not compatible with alignment: %s not found name %s is too long for PHYLIP tree format (max %d chars) input tree is unrooted and has no distances. Cannot align sequences tree not compatible with alignment (%d sequences in alignment and %d in tree Wrong format in tree file %s cannot open %s r clustalw.hlp =filename =string =f =n strandendout strandendin helixendout helixendin terminalgap loopgap strandgap helixgap secstrout nosecstr2 nosecstr1 range seqno_range seqnos case outorder outfile outputtree output debug bootlabels tossgaps kimura seed transweight score topdiags pairgap window ktuple pwgapext pwgapopen pwdnamatrix pwmatrix gapdist maxdiv hgapresidues novgap nohgap nopgap endgaps gapext gapopen noweights negative dnamatrix matrix sequences profile type batch interactive convert quicktree tree bootstrap usetree2 newtree2 usetree1 newtree1 usetree newtree align options check help profile2 profile1 infile none both mask structure dist nj fasta nexus phylip pir gde gcg absolute percent on off upper lower aligned input branch node dna protein HFY FVLIM NEQHRK NDEQHK SNDEQK SGND STPA STNK SAG ATV CSA FYW HY MILF MILV QHRK NDEQ NHQK NEQK STA Error: unknown option %c%s Error: parameter required for /%s Error: too many command line arguments No help found in help file Press [RETURN] to continue Press [RETURN] to continue or X to stop 0123456789ABCDEFGHIJKLMNOPQRSTUVWXYZ >>HELP Cannot open help file [%s] Cannot open file [%s] Cannot find matrix file [%s] Enter name of the matrix file Sequence %d: %-*s %6.d %s aa bp Sequences assumed to be %s No sequences in file! Bad format? NBRF/PIR, EMBL/SwissProt, Pearson (Fasta), GDE, Clustal, GCG/MSF, RSF. 7 formats accepted: Sequences should all be in 1 file. Total no. of seqs =%d No. of seqs in profile=%d No. of seqs=%d %c You must read in profile number 1 first Cannot open output file [%s] w [%s]: Enter new name to avoid overwriting Output file name is the same as input file. Bad output file [%s] Done checking......... check... %s %d - %d no range found .... strange, istart = %d formula %d suggestion istart - pregaps + tmpStart - ntermgaps = %d - %d + %d - %d pregaps = %d ngaps = %d tmpStart = %d istart = %d len = %d fres = %d Name : %s %[^/]/%d-%d ; end; %-*s %s/%d-%d %-*s matrix gap= -; PROTEIN DNA interleave datatype= " symbols=" format missing=? dimensions ntax=%d nchar=%d; BEGIN DATA; #NEXUS cannot alloc memory for rnum %-10s %6d %6d Truncating sequence names to 10 characters for PHYLIP output. Truncating sequence names to 10 characters for PHYLIP output. Names in the PHYLIP format file are NOT unambiguous. * %s %s >P1; >DL; "GM_%-*s "SS_%-*s %s/%d-%d %s %% # Enter a name for the Fasta output file Enter a name for the NEXUS output file nxs Enter a name for the GDE output file Enter a name for the PHYLIP output file phy Enter a name for the GCG output file msf Enter a name for the NBRF/PIR output file Enter a name for the CLUSTAL output file aln You must select an alignment output format -interactive -case=upper \ -case=lower \ -outorder=input \ -outorder=aligned \ -outfile=%s \ -output=nexus \ -output=phylip \ -output=pir \ -output=gde \ -output=gcg \ -transweight=%.2f \ -gapdist=%d \ -hgapresidues=%s \ -novgap \ -nohgap \ -nopgap \ -negative \ -endgaps \ -maxdiv=%d \ -gapext=%.2f \ -gapopen=%.2f \ -matrix=%s \ -pwgapext=%.2f \ -pwgapopen=%.2f \ -pwmatrix=%s \ -score=absolute \ -score=percent \ -topdiags=%d \ -pairgap=%d \ -window=%d \ -ktuple=%d \ -quicktree \ -type=protein \ -type=dna \ -profile2=%s \ -profile1=%s\ -infile=%s \ clustalw \ Enter a name for the parameter output file [%s]: par %8.0f %5d: %-*s # # # Percent Identity Matrix - created by Clustal%s # # %s Bad option for /strandendout (must be integer) Bad option for /strandendin (must be integer) Bad option for /helixendout (must be integer) Bad option for /helixendin (must be integer) Bad option for /terminalgap (must be integer) Bad option for /loopgap (must be integer) Bad option for /strandgap (must be integer) Bad option for /helixgap (must be integer) Unknown bootlabels type %s Unknown OUTPUT ORDER type %s Bad option for /pwgapext (must be real number) Bad option for /pwgapopen (must be real number) Bad option for /transweight (must be real number) Bad option for /gapext (must be real number) Bad option for /gapopen (must be real number) setrange: Syntax Error: Cannot set range, should be from:to %d:%d Unknown Sequence range option %s comparing param_arg[setseqno_range]= %s comparing Unknown SEQNO option %s Unknown case %s Bad option for /debug (must be integer) Bad option for /gapdist (must be integer) Bad option for /maxdiv (must be integer) clustalw iub id gonnet pam blosum Bad option for /window (must be integer) Bad option for /topdiags (must be integer) Bad option for /pairgap (must be integer) Bad option for /ktuple (must be integer) Unknown OUTPUT TREE type: %s Unknown OUTPUT type: %s temp = %d; seed = %u; Bad option for /seed (must be integer) %d Unknown SCORE type: %s Guide tree file created: [%s] Enter name for new GUIDE TREE file dnd Aligning... Start of Pairwise alignments Less than 2 sequences in memory. Phylogenetic tree cannot be built. No sequences in memory. Load sequences first. /%d-%d >%-s %d %s %-*s !GM_%-*s %s !SS_%-*s %s CLUSTAL %s multiple sequence alignment // Name: %s oo Len:%5d Check:%6ld Weight: %.1f Check:%6ld .. P N MSF:%5d Type: PileUp Fasta-Alignment file created [%s] NEXUS-Alignment file created [%s] GDE-Alignment file created [%s] PHYLIP-Alignment file created [%s] GCG-Alignment file created [%s] NBRF/PIR-Alignment file created [%s] CLUSTAL-Alignment file created [%s] Consensus length = %d Seqrange %d is more than the %d setting it to %d seqrange numers are not set properly, using default.... %d%[ :,-]%d Use the existing GUIDE TREE file, %s (y/n) ? [y]: Warning: ignoring gap penalty mask for a list of sequences Warning: ignoring secondary structure for a list of sequences No sequences in memory. Input sequences first. No profile in memory. Input 1st profile first. Cannot open tree file [%s] Enter a name for the guide tree file [%s]: Enter name for new GUIDE TREE file for profile 2 Enter name for new GUIDE TREE file for profile 1 Use the existing GUIDE TREE file for Profile 2, %s (y/n) ? [y]: Use the existing GUIDE TREE file for Profile 1, %s (y/n) ? [y]: No input file(s) specified Invalid option /newtree2. Invalid option /usetree2. Invalid option /newtree1. Cannot align profiles. No tree file specified Invalid option /usetree1. Cannot align sequences. No tree file specified Cannot convert sequences. No input file Cannot align sequences. No input file Bad option for /bootstrap (must be integer) Cannot bootstrap tree. No input alignment file Cannot draw tree. No input alignment file Cannot align profiles. No input file No sequences read from profile 2 Only 1 profile file (profile 2) specified. Bad profile 2 file name Bad profile 1 file name No. of seqs. read = %d. No alignment! Bad sequence file name Unknown sequence type %s Sequence type explicitly set to DNA Sequence type explicitly set to Protein OR %s =%s %c%s%s clustalw option list:- CLUSTAL %s Multiple Sequence Alignments Sequence:%d Score:%d Group %d: Delayed Group %d: Sequences:%4d Score:%d There are %d groups Start of Multiple Alignment new weights sequence %d: %d Sequences:%d Score:%d Start of Initial Alignment Sequences (%d:%d) Aligned. Score: %d Sequences (%d:%d) Aligned. Score: %d CompScore: %d #<go %d ge %d matrix %s Error in aln_path Type 2,2: midj %d Type 2,1: midj %d Type 1,2: midj %d Type 1,1: midj %d A %d B %d M %d N %d midi %d go1 %d go2 %d %d %d %c Matrix %s Gap Open1 %d Gap Open2 %d Gap Extend1 %d Gap Extend2 %d matavscore %d Error: matrix %s not found pcid %3.1f scale %3.1f pcid %d matrix %d Series matrix not found for sequence percent identity = %d. (Using first matrix in series as a default.) This alignment may not be optimal! SUGGESTION: Check your matrix series input file and try again. 9@ A@ 4@ >@ D@ N@ T@%d %d logmin %f logdiff %f ?sequences profile 2: sequences profile 1: mean tmat %3.1f ABCDGHKMNRSTUVWXY ABCDEFGHIKLMNPQRSTVWXYZ nucleic acid %c in matrices.h is not recognised residue %c in matrices.h is not recognised min %d max %d average score %d average match score %d average mismatch score %d maxres %d residue %c in matrix %s not recognised too many entries in matrix %s wrong format in matrix %s in %s - single matrix expected. CLUSTAL_SERIES comparison matrix not specified Bad format in matrix file %s in file %s: lower limit is greater than upper (%d-%d) Bad format in file %s %d %d %s MATRIX NEXUS PHYLIP USER RSF Pileup/MSF Clustal GDE Pearson PIR EMBL/Swiss-Prot unknown ABCDEFGHIKLMNPQRSTUVWXYZ- // %s%s bad gap penalty mask format bad secondary structure format Found gap penalty mask in alignment file: !GM Use it to set local gap penalties Found secondary structure in alignment file: !SS GM_ SS_ STRAND HELIX %s%d%d %d%d%d%s%s%s %d%d%d sequence name SQ ID PIR format sequence end marker '*' missing for one or more sequences. PIR format sequence end marker '*' missing for one or more sequences. GM %s FT feature 333333?ACGTUN #NEXUS !!RICH_SEQUENCE MSF !!NA_MULTIPLE_ALIGNMENT !!AA_MULTIPLE_ALIGNMENT PILEUP CLUSTAL Multiple sequences found with same name, %s (first %d chars are significant) Cannot read nexus format Sequence format is %s Could not open sequence file (%s) file://%s Enter the name of the sequence file @(Partial alignment) Sequences (%d:%d) Not Aligned Sequences (%d:%d) Aligned. Score: %lg ? getting robust and reliable trees. of divergence you will have great difficulty Note: Use option 3 with caution! With this degree or 3) turn off the correction. or 2) use the PHYLIP package SUGGESTIONS: 1) remove the most distant sequences were out of range for the distance correction. %d of the distances out of a total of %d %6.3f %6d joins SEQ:%4d (%9.5f) Node:%4d (%9.5f) Cycle%4d (Last cycle, trichotomy): SEQ:%4d (%9.5f) Node:%4d (%9.5f) SEQ:%4d (%9.5f) joins Node:%4d (%9.5f) joins -C 6? Cycle%4d = iACycle 1 = SEQ: 1 (%9.5f) joins SEQ: 2 (%9.5f) Numbers in parentheses are branch lengths This is an UNROOTED tree Mol. Biol. Evol., 4(4), 406-425 A New Method for Reconstructing Phylogenetic Trees. The Neighbor-joining Method: Saitou, N. and Nei, M. (1987) Neighbor-joining Method ) :%7.5f) , [%d] :%7.5f :%7.5f, ( ) :%7.5f) , :%7.5f, %.*s ( %1d %7d . * %4d vs.%4d DIST = %6.4f; length = %6.0f p@ @@(\?? ? Page 75. Cambridge University Press, Cambridge, England. The Neutral Theory of Molecular Evolution. Kimura, M. (1983) Distances up tp 0.75 corrected by Kimura's empirical method: All sites with gaps (in any sequence) deleted Length = number of sites used in comparison DIST = percentage divergence (/100) ACGTU ENDBLOCK; ; TRICHOTOMY (%d:%7.5f,%d:%7.5f); UTREE PAUP_1= ; %d %s %d %s, TRANSLATE BEGIN TREES; #NEXUS ; (%s:%7.5f,%s:%7.5f); %4d vs.%4d: DIST = %7.4f; p = %6.4f; q = %6.4f; length = %6.0f @ ? WARNING: sequences %d and %d are non-overlapping J. Mol. Evol., 16, 111-120. nucleotide sequences. substitutions through comparative studies of rates of base A simple method for estimating evolutionary Kimura, M. (1980) Distances corrected by Kimura's 2 parameter model: All sites with gaps (in any sequence) deleted! q = rate of transversion p = rate of transition (A <-> G; C <-> T) (%s:%0.5f,%s:%0.5f); perc identity matrix file created: [%s] Nexus tree file created: [%s] Distance matrix file created: [%s] Phylogenetic tree file created: [%s] Enter name for % Identity matrix output file pim Enter name for NEXUS tree output file tre Enter name for distance matrix output file dst Enter name for PHYLIP tree output file ph Enter name for CLUSTAL tree output file Alignment has only %d sequences You must load an alignment first Bootstrap output file completed [%s] or 3) use the PHYLIP package. or 2) remove the most distant sequences SUGGESTIONS: 1) turn off the correction This may not be fatal but you have been warned! This affected %d out of %d bootstrap trials. WARNING: %ld of the distances out of a total of %ld times %ld Each dot represents 10 trials Numbers show occurences in bootstrap samples. the dots show the other the stars in each line show 1 group; Each column is 1 sequence; defining 2 groups. Each row represents 1 tree cycle; Diagrammatic representation of the above tree: Number of bootstrap trials = %7d Enter number of bootstrap trials Random number generator seed = %7u Enter seed no. for random number generator Bootstrap Confidence Limits treb phb Enter name for bootstrap output file njb You must select either clustal or phylip or nexus tree output format Out of memory Bad call to ckrealloc Bad call to ckfree %s: ERROR: Min. value=%.1f ERROR: Max. value=%.1f %s (%.1f-%.1f) [%.1f]: ERROR: Min. value=%d ERROR: Max. value=%d %s (%d..%d) [%d]: Enter system command ( ( ( ( ( H h ( ( ( ( H H zA ~A CorExitProcess mscoree.dll cmd.exe command.com /c COMSPEC B B EEE50 P (8PX 700WP `h```` ppxxxx ( n u l l ) (null) e+000 ~PA GAIsProcessorFeaturePresent KERNEL32 B B B B ^B bB B B Microsoft Visual C++ Runtime Library Program: ... <program name unknown> A buffer overrun has been detected which has corrupted the program's internal state. 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