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A[y]XPSjXnN!<ye[_]UE E5jjh6` uu5茱5jjh<48j~UE E5j jh#6 uu5:5jjh<4 UE E5j jh-6 uu55jjh<4虲 U E E5j K uu5觰ÐUWVS rgڌB} EP<0 E]0 ؉Eu ރ >QUB60 t EE9Eu(I  j!uN~ 0 4+C9u 50 = j跰U]su}1)Eu]u}]1֍v'G;}r]u}]Ð&U]藱zsu})EHt41&G9}u@]u}]ÐUSRPtPЋCuX[]ÐUS r Y[]STANEQKNHQKNDEQMILVMILFHYFYWCSAATVSAGSTNKSTPASGNDSNDEQKNDEQHKNEQHRKFVLIMHFYproteindnanodebranchinputalignedlowerupperoffpercentabsolutegcggdepirphylipnexusnjstructuremaskbothnoneinfileprofile1profile2checkoptionsalignnewtreeusetreenewtree1usetree1newtree2usetree2bootstrapquicktreeconvertinteractivebatchtypeprofilesequencesnegativenoweightsendgapsnopgapnohgapnovgaphgapresiduesmaxdivgapdistpwmatrixpwdnamatrixpwgapopenpwgapextktuplewindowpairgaptopdiagsscoretransweightseedkimuratossgapsbootlabelsdebugoutputoutputtreeoutfileoutordercaseseqnosnosecstr1nosecstr2secstrouthelixgapstrandgaploopgapterminalgaphelixendinhelixendoutstrandendinstrandendoutave_grp_idcosmetickkoutputfirst=n =f =string =filename Error: unknown option %c%s Unknown SCORE type: %s temp = %d; seed = %u; Unknown OUTPUT type: %s blosumpamgonnetiubclustalw Unknown case %s Unknown SEQNO option %s %f Unknown bootlabels type %s PATHCannot open help file [%s]No help found in help fileHELPPress [RETURN] to continueCannot open file [%s] Unknown sequence type %s Bad sequence file nameBad profile 1 file nameBad profile 2 file nameInvalid option /usetree1.Invalid option /newtree1.Invalid option /usetree2.Invalid option /newtree2.No input file(s) specifiedEnter name of the matrix fileCannot find matrix file [%s] 7 formats accepted: DNAPROTEINSequences assumed to be %sNo. of seqs=%dNo. of seqs in profile=%dTotal no. of seqs =%dbpaaSequence %d: %-*s %6.d %sCannot open output file [%s]Bad output file [%s]dndnseqs: %d Cannot open tree file [%s]%d %d %d %d !SS_%-*s %s !GM_%-*s %s %-*s %sPileUp MSF:%5d Type: Check:%6ld .. // %-*s #NEXUS BEGIN DATA; dimensions ntax=%d nchar=%d; format missing=? symbols="interleave datatype=DNA PROTEIN gap= -; matrix; end; %6d %6d %-10s >DL;>P1;%s %s #%%"SS_%-*s "GM_%-*s alnmsfphynxsConsensus length = %doutput first sequence only clustalw \ -infile=%s \ -profile1=%s\ -profile2=%s \ -type=dna \ -type=protein \ -quicktree \ -ktuple=%d \ -window=%d \ -pairgap=%d \ -topdiags=%d \ -score=percent \ -score=absolute \ -pwmatrix=%s \ -pwgapopen=%.2f \ -pwgapext=%.2f \ -matrix=%s \ -gapopen=%.2f \ -gapext=%.2f \ -maxdiv=%d \ -endgaps \ -negative \ -nopgap \ -nohgap \ -novgap \ -hgapresidues=%s \ -gapdist=%d \ -transweight=%.2f \ -output=gcg \ -output=gde \ -output=pir \ -output=phylip \ -output=nexus \ -outfile=%s \ -outorder=aligned \ -outorder=input \ -case=lower \ -case=upper \ -interactive 1.A quick start might be incorrect. An example: 3.Commonly used options @ alignment1.aln alignment2.aln alignment3.aln Error: too many command line arguments Error: parameter required for /%s use -options to see the parameters Bad option for /seed (must be integer) Unknown OUTPUT TREE type: %s Bad option for /ktuple (must be integer) Bad option for /pairgap (must be integer) Bad option for /topdiags (must be integer) Bad option for /window (must be integer) Bad option for /maxdiv (must be integer) Bad option for /gapdist (must be integer) Bad option for /debug (must be integer) Bad option for /gapopen (must be real number) Bad option for /gapext (must be real number) Bad option for /transweight (must be real number) Bad option for /pwgapopen (must be real number) Bad option for /pwgapext (must be real number) Unknown OUTPUT ORDER type %s Bad option for /helixgap (must be integer) Bad option for /strandgap (must be integer) Bad option for /loopgap (must be integer) Bad option for /terminalgap (must be integer) Bad option for /helixendin (must be integer) Bad option for /helixendout (must be integer) Bad option for /strandendin (must be integer) Bad option for /strandendout (must be integer) Bad option for /ave_grp_id (must be integer) Bad option for /cosmetic penalty (must be integer) Bad option for /outputfirst (must be integer) /usr/share/clustalx:/usr/local/share/clustalx0123456789ABCDEFGHIJKLMNOPQRSTUVWXYZPress [RETURN] to continue or X to stopSequence type explicitly set to ProteinSequence type explicitly set to DNA No. of seqs. read = %d. No alignment! Only 1 profile file (profile 2) specified.No sequences read from profile 2Cannot draw tree. No input alignment fileCannot bootstrap tree. No input alignment fileBad option for /bootstrap (must be integer) Cannot align sequences. No input fileCannot convert sequences. No input fileCannot align sequences. No tree file specifiedCannot align profiles. No input fileCannot align profiles. No tree file specified Sequences should all be in 1 file. NBRF/PIR, EMBL/SwissProt, Pearson (Fasta), GDE, Clustal, GCG/MSF, RSF. No sequences in file! Bad format?You must read in profile number 1 firstOutput file name is the same as input file. Enter new name to avoid overwriting No sequences in memory. Load sequences first. Enter name for new GUIDE TREE file Start making pairwise alignments Guide tree file created: [%s] No profile in memory. Input 1st profile first.No sequences in memory. Input sequences first.Warning: ignoring secondary structure for a list of sequencesWarning: ignoring gap penalty mask for a list of sequences Use the existing GUIDE TREE file, %s (y/n) ? [y]: Guide tree file created: [%s]Less than 2 sequences in memory. Phylogenetic tree cannot be built. Enter a name for the guide tree file [%s]: Use the existing GUIDE TREE file for Profile 1, %s (y/n) ? [y]: Use the existing GUIDE TREE file for Profile 2, %s (y/n) ? [y]: Enter name for new GUIDE TREE file for profile 1 Enter name for new GUIDE TREE file for profile 2 CLUSTAL %s multiple sequence alignment Name: %s oo Len:%5d Check:%6ld Weight: %.1f Truncating sequence names to 10 characters for PHYLIP output. Names in the PHYLIP format file are NOT unambiguous.Truncating sequence names to 10 characters for PHYLIP output.You must select an alignment output format Enter a name for the CLUSTAL output file Enter a name for the NBRF/PIR output file Enter a name for the GCG output file Enter a name for the PHYLIP output file Enter a name for the GDE output file Enter a name for the NEXUS output file CLUSTAL-Alignment file created [%s]NBRF/PIR-Alignment file created [%s]GCG-Alignment file created [%s]PHYLIP-Alignment file created [%s]GDE-Alignment file created [%s]NEXUS-Alignment file created [%s] Enter a name for the parameter output file [%s]: PCMA - Profile Consistency Multiple sequence Alignment To align a sequence set in fasta format, use the following command: pcma Two output files will be generated: .aln - A multiple sequence alignment in clustal format .dnd - A dendrogram in phylip format 2.Usage: pcma The first command line argument should be the name of the file containing FASTA format sequences. One IMPORTANT notice is that the sequences should not contain gap characters in them, otherwise the results Options are in the format of -optionName or -optionName=option. NOTE that there should be no space(s) between "optionName", "=" and "option". Although many of the original ClustalW options are supported in PCMA, changes from default parameters are not recommended for most of them. pcma yfp.fa -ave_grp_id=50 -outfile=yfp.pcma50.aln -ave_grp_id= Threshold of PERCENTAGE sequence identity above which neighboring groups are aligned by ClustalW and below which neighboring groups are subject to profile consistency measure. If the sequence number is very large, a decrease of the threshold from the default value is recommended. Range [0..100] Default: -ave_grp_id=40 -outfile= Name of the output alignment. If this option is not used, the output alignment will be in clustal format with .aln suffix -output= The output alignment format. Default: -output=clustal Other formats include gcg, phylip and pir. -help or -options Help and options. 4.Newly added function for PCMA PCMA now supports the alignment of several alignments. In this case, the first command-line parameter should be a file containing a list of file names of the alignments to be aligned together. To make this format distinct from a fasta format sequence file, the first line should start with a character "@". Each of the other lines contains the file name of an alignment. Here, input alignments CAN have gap characters (usually they do). For example, below is the content of file "alnlist": PCMA (command: pcma alnlist) will generate a new alignment named "alnlist.aln". "+4=BzDABCDEFGHIKLMNPQRSTUVWXYZ-unknownEMBL/Swiss-ProtPIRPearsonGDEClustalPileup/MSFRSFUSERPHYLIP//!SS!GMbad gap penalty mask formatIDFTHELIXSTRANDSQfeaturesequenceSS_GM_%s%d%d%d%d%d%s%s%s%d%d%dfilecount: %d Cannot read nexus formatACGTUNCLUSTALPILEUP!!AA_MULTIPLE_ALIGNMENT!!NA_MULTIPLE_ALIGNMENT!!RICH_SEQUENCE#NEXUSCLUSTALIST format input @ alignment listFound secondary structure in alignment file: Use it to set local gap penalties Found gap penalty mask in alignment file: bad secondary structure formatEnter the name of the sequence fileCould not open sequence file %sCould not open the sequence file [%s]number of input alignments: %d total number of sequences: %d There are two sequences with the same name: %s Multiple sequences found with same name, %s (first %d chars are significant)PIR format sequence end marker '*' missing for one or more sequences.PIR format sequence end marker '*' missing for one or more sequences.;;ED@;;BVoUUUUV7V[VVVVV333333??(Partial alignment)Start making multiple sequence alignment ave_grp_id: %d; KK: %d cosmetic: %d Average percentage group identity threshold is %d There are %d pre-aligned groups Start progressive alignment of pre-aligned groups Error: abstract sequence of the right child do not exist. set %d Error: abstract sequence of the left child do not exist. set %d Error: name does not match: %s Start making multiple alignment There are %d sequences OUTPUT_ORDER: %d average score: %5.3f %5.3f ********* group %d alignment length: %d %s Start generating libray ++++++++++++ Start extending library SET: %d %d %s %d %s Sequence:%d Score:%dsequence %d: %d new weights Start of Initial Alignment Sequences:%d Score:%dOut of memory Bad call to ckrealloc Bad call to ckfree %s: %s (%.1f-%.1f) [%.1f]: ERROR: Max. value=%.1f ERROR: Min. value=%.1f %s (%d..%d) [%d]: ERROR: Max. value=%d ERROR: Min. value=%d Enter system commandYou must load an alignment firstAlignment has only %d sequences Enter name for CLUSTAL tree output file Enter name for PHYLIP tree output file Enter name for distance matrix output file Enter name for NEXUS tree output file Phylogenetic tree file created: [%s]Distance matrix file created: [%s]Nexus tree file created: [%s]%d of the distances out of a total of %d were out of range for the distance correction. SUGGESTIONS: 1) remove the most distant sequences or 2) use the PHYLIP package or 3) turn off the correction. Note: Use option 3 with caution! With this degree of divergence you will have great difficulty getting robust and reliable trees. Saitou, N. and Nei, M. (1987) A New Method for Reconstructing Phylogenetic Trees. Mol. Biol. Evol., 4(4), 406-425 Numbers in parentheses are branch lengths Cycle 1 = SEQ: 1 (%9.5f) joins SEQ: 2 (%9.5f) Cycle%4d (Last cycle, trichotomy): You must select either clustal or phylip or nexus tree output format Enter name for bootstrap output file Bootstrap Confidence Limits Enter seed no. for random number generator Random number generator seed = %7u Enter number of bootstrap trials Number of bootstrap trials = %7d Diagrammatic representation of the above tree: Each row represents 1 tree cycle;the stars in each line show 1 group; Numbers show occurences in bootstrap samples. Each dot represents 10 trials WARNING: %ld of the distances out of a total of %ld times %ld This affected %d out of %d bootstrap trials. This may not be fatal but you have been warned! SUGGESTIONS: 1) turn off the correction or 2) remove the most distant sequences or 3) use the PHYLIP package.Bootstrap output file completed [%s] DIST = percentage divergence (/100) p = rate of transition (A <-> G; C <-> T) q = rate of transversion Length = number of sites used in comparison All sites with gaps (in any sequence) deleted! Distances corrected by Kimura's 2 parameter model: A simple method for estimating evolutionary substitutions through comparative studies of WARNING: sequences %d and %d are non-overlapping %4d vs.%4d: DIST = %7.4f; p = %6.4f; q = %6.4f; length = %6.0f All sites with gaps (in any sequence) deleted Distances up tp 0.75 corrected by Kimura's empirical method: The Neutral Theory of Molecular Evolution. Page 75. Cambridge University Press, Cambridge, England.%4d vs.%4d DIST = %6.4f; length = %6.0f phdsttre%6.3f Neighbor-joining Method The Neighbor-joining Method: This is an UNROOTED tree Cycle%4d = Node:%4d (%9.5f) joins SEQ:%4d (%9.5f) joins Node:%4d (%9.5f) SEQ:%4d (%9.5f) Node:%4d (%9.5f) SEQ:%4d (%9.5f) joinsnjbphbtreb defining 2 groups. Each column is 1 sequence; the dots show the other #NEXUS BEGIN TREES; TRANSLATE %d %s, %d %s ; UTREE PAUP_1= (%d:%7.5f,%d:%7.5f);:%7.5f[%d]TRICHOTOMY ENDBLOCK; :%7.5f,:%7.5f)(%s:%7.5f,%s:%7.5f);( :%7.5f, %.*s:%7.5f) %7d%1d Kimura, M. (1980)rates of basenucleotide sequences. J. Mol. Evol., 16, 111-120. Kimura, M. (1983)(%s:%0.5f,%s:%0.5f); ACGTU%s%dm: %d n: %d %d %d @OG?`@>?@? A;D-C6?ư>(\?mean tmat %3.1f sequences profile 1: sequences profile 2: %d %d logmin %f logdiff %f pcid %d matrix %d pcid %3.1f scale %3.1f Error: matrix %s not found matavscore %d Matrix %s %c Error in aln_path Type 1,1: midj %d Type 1,2: midj %d Type 2,1: midj %d Type 2,2: midj %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.Gap Open1 %d Gap Open2 %d Gap Extend1 %d Gap Extend2 %d A %d B %d M %d N %d midi %d go1 %d go2 %d BpB BAA BA?matrix %s go %d ge %d tmat: %d %d %f Sequences (%d:%d) Aligned. Score: %d CompScore: %d Using variable zones to set gap penalties (pcid = %d) gap open %d gap ext %d gaps: gap_pos: Opening penalties: %d:%d Extension penalties: cannot open %sWrong format in tree file %sContinue group: %d >%s sum: %5.3f tree not compatible with alignment (%d sequences in alignment and %d in treeinput tree is unrooted and has no distances. Cannot align sequencesname %s is too long for PHYLIP tree format (max %d chars)tree not compatible with alignment: %s not foundThe following sequences are too divergent to be aligned: %s and %s (distance %1.3f) (All distances should be between 0.0 and 1.0) This may not be fatal but you have been warned! SUGGESTION: Remove one or more problem sequences and try againassign nodes: sequences already exist ?ABCDEFGHIKLMNPQRSTVWXYZABCDGHKMNRSTUVWXYmaxres %d average mismatch score %d average match score %d average score %d min %d max %d CLUSTAL_SERIESMATRIX%d %d %sBad format in file %s Bad format in matrix file %s too many entries in matrix %swrong format in matrix %s residue %c in matrices.h is not recognisednucleic acid %c in matrices.h is not recognisedcomparison matrix not specifiedin file %s: lower limit is greater than upper (%d-%d) in %s - single matrix expected.residue %c in matrix %s not recognisedError: matrix blosum30 not found Alignment Score %d0123456789---TRPPHETYRMETLEUVALALACYSGLYPROTHRASNGLNASPGLUHISARGLYSASXGLXUNK***...alcomp2: %d %d %d %d %6.1fToo many bisections in rtbisstring too long:FATAL%7.4f,FATAL - execution terminated Not enough memory: %d No such file: "%s" CLUSTAL Wrong nal, was: %d, now: %d Names do not match, was: %s, now: %s wrong len for %sNo alignments read freqInt started... not good number for AA gap number>total number sumNC = %d alilen = %d %f %f NSTACK too small in sort.-WFYMLIVACGPTSNQDEHRKBZX*.wfymlivacgptsnqdehrkbzxcolumn-column score calculation method(-f): 1, 3_21; 2, 3_22 ...., 8, 3_28 adjustment of gap extension penalty depending on gap content in opposite column (-e): 0, no adjustment; 1, adjust gap extension reduction of column-column scores according to gap content (-r): 0, no reduction; 1, adjust scores gap content(-g) to eliminate a column must be no more than 1 and more than 0 score_scale: %8.5f; lambda_al: %8.5f; lambda_u: %8.5f Root must be bracketed for bisection in rtbismatrix has more than 24 columns: FATALmatrix has more than 24 rows: FATALallocation failure in ivector()allocation failure in lvector()allocation failure in dvector()allocation failure 1 in cmatrix()allocation failure 2 in cmatrix()allocation failure 1 in imatrix()allocation failure 2 in imatrix()allocation failure 1 in dmatrix()allocation failure 2 in dmatrix()allocation failure 1 in d3tensor()allocation failure 2 in d3tensor()allocation failure 3 in d3tensor()Error with reading alignment: %d Bad sequence number: %d of %d 9B.? !? !|= >YS??'@[Ch㈵> j C.PG?@A>ɗYuH—ngɗHЗ>|R>`ЗHHHHHH>ɗYuH—ngɗHЗ>|R>`З=Du| K/(gRn`Y6=Du| K/(gRn`Y6͘ɘɘɘɘɘɘɘɘɘɘɘɘɘɘɘɘɘɘɘ!՘ɘݘɘ ɘјŘ٘%LHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHlpTtdH`\Hx|HhPDX******* %d ******** %8.5fi%d i %d j %d ============ memory for SN: %d * %d Group %d and Group %d %5c%c %5dPreparing lib for group i: %d j: %d seqnum: %d %d seqlength: %d %d group number exceeds the boundary: max(%d, %d) >= %dThe number of alignments computed is too largesubalignment %d score %d average score %d average id %d Ran out of near memory: %d/%ld rl: %d; stari: %d; endi: %d cl: %d; starj: %d; endj: %d gaps %d nonegaps %didentity: %d %d tpairs %d idpairs %d first: %d Cannot open %s.se1: %d; se2: %d gap penalties: %d %d %d SET: set path %d: %d %d Error in aln_path: %d Error in aln path: %d #########alignment length: %d gaps: %d nonegaps: %d seqlengths %d %d first: %d; second: %d global alignment %d %d score %d average score %d average id %d prfalign2 score: %d Secondary StructureGap Penalty MaskStructure and Penalty MaskNone .. Interrupt Error: signal 2. Multiple Alignments 4. Phylogenetic trees H. HELP Your choice Unrecognised Command Slow/AccurateFast/ApproximateSLOWFAST = ON = OFF OFFON H. HELP (loaded)= YES = NO 3. Output in alignment = %s H. HELP Helix Penalty Currently: %d Enter number 1. %s 2. %s 3. %s 4. %s H. HELP -- Current output is %s -- 1. Input an alignment 4. Draw tree now 5. Bootstrap tree NODE LABELSBRANCH LABELSUPPERLOWERINPUT FILEALIGNEDNo sequences loaded= FAST = SLOW Gap Penalty Currently: %d K-tuple Currently: %d Top diagonals Currently: %d Window size Currently: %d Min Identity Currently: %d %d. %s (file = %s) FATAL ERROR: ERROR: WARNING: ******************************************************************** PCMA - Profile Consistency Multiple sequence Alignment 1. Sequence Input From Disc 3. Profile / Structure Alignments S. Execute a system command X. EXIT (leave program) ****** MULTIPLE ALIGNMENT MENU ****** 1. Do complete multiple alignment now (%s) 2. Produce guide tree file only 3. Do alignment using old guide tree file 4. Toggle Slow/Fast pairwise alignments = %s 5. Pairwise alignment parameters 6. Multiple alignment parameters 7. Reset gaps before alignment? 8. Toggle screen display = %s 9. Output format options S. Execute a system command or press [RETURN] to go back to main menu ****** PROFILE AND STRUCTURE ALIGNMENT MENU ****** 1. Input 1st. profile 2. Input 2nd. profile/sequences 3. Align 2nd. profile to 1st. profile 4. Align sequences to 1st. profile (%s) 5. Toggle Slow/Fast pairwise alignments = %s 6. Pairwise alignment parameters 7. Multiple alignment parameters 8. Toggle screen display = %s 0. Secondary structure options ********* SECONDARY STRUCTURE OPTIONS ********* 1. Use profile 1 secondary structure / penalty mask 2. Use profile 2 secondary structure / penalty mask 4. Helix gap penalty :%d 5. Strand gap penalty :%d 6. Loop gap penalty :%d 7. Secondary structure terminal penalty :%d 8. Helix terminal positions within :%d outside :%d 9. Strand terminal positions within :%d outside :%d Enter number (or [RETURN] to exit)Strand Gap Penalty Currently: %d Loop Gap Penalty Currently: %d Secondary Structure Terminal Penalty Currently: %d Helix Terminal Positions Currently: within helix: %d outside helix: %d Enter number of residues within helixEnter number of residues outside helixStrand Terminal Positions Currently: within strand: %d outside strand: %d Enter number of residues within strandEnter number of residues outside strand ********* Secondary Structure Output Menu ********* Enter number (or [RETURN] to exit)****** PHYLOGENETIC TREE MENU ****** 2. Exclude positions with gaps? 3. Correct for multiple substitutions? 6. Output format options ****** Format of Phylogenetic Tree Output ****** 1. Toggle CLUSTAL format tree output = %s 2. Toggle Phylip format tree output = %s 3. Toggle Phylip distance matrix output = %s 4. Toggle Nexus format tree output = %s 5. Toggle Phylip bootstrap positions = %s ********* Format of Alignment Output ********* 1. Toggle CLUSTAL format output = %s 2. Toggle NBRF/PIR format output = %s 3. Toggle GCG/MSF format output = %s 4. Toggle PHYLIP format output = %s 5. Toggle NEXUS format output = %s 6. Toggle GDE format output = %s 7. Toggle GDE output case = %s 8. Toggle CLUSTALW sequence numbers = %s 9. Toggle output order = %s 0. Create alignment output file(s) now? T. Toggle parameter output = %s ********* PAIRWISE ALIGNMENT PARAMETERS ********* Slow/Accurate alignments: 1. Gap Open Penalty :%4.2f 2. Gap Extension Penalty :%4.2f 3. Protein weight matrix :%s 4. DNA weight matrix :%s Fast/Approximate alignments: 5. Gap penalty :%d 6. K-tuple (word) size :%d 7. No. of top diagonals :%d 8. Window size :%d 9. Toggle Slow/Fast pairwise alignments Gap Open Penalty Currently: %4.2f Gap Extension Penalty Currently: %4.2f ********* MULTIPLE ALIGNMENT PARAMETERS ********* 1. Gap Opening Penalty :%4.2f 2. Gap Extension Penalty :%4.2f 3. Delay divergent sequences :%d %% 4. DNA Transitions Weight :%1.2f 5. Protein weight matrix :%s 6. DNA weight matrix :%s 7. Use negative matrix :%s 8. Protein Gap Parameters Gap Opening Penalty Currently: %4.2f This value is not to be changed in ClustalCoffee Transition Weight Currently: %1.2f ********* PROTEIN GAP PARAMETERS ********* 1. Toggle Residue-Specific Penalties :%s 2. Toggle Hydrophilic Penalties :%s 3. Hydrophilic Residues :%s 4. Gap Separation Distance :%d 5. Toggle End Gap Separation :%s Hydrophilic Residues Currently: %s Enter residues (or [RETURN] to quit)Gap Separation Distance Currently: %d ********* %s WEIGHT MATRIX MENU ********* -- Current matrix is the %s aӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳӳɳӳӳӳӳӳɳh}Ƕ66"Kezֺֺֺֺֺĺֺֺֺֺֺֺֺֺĺֺֺֺֺֺֺֺֺֺֺֺֺֺн D~*D((((((((((((((((((((((((((D((((((D44444444"44444444"44444444P44444P<HT`looc2~dB|6)%1MMMMMM;MMMMMMMM;+7C-----------------pcma_helpL @  Po$ooPn~΋ދ.>N^n~Όތ.>N^n~΍ލ.>N^n~ PpA@ AL>(d gonnetiubGPSNDQEKRpA@ A=gonnetiub?o!&g+058<@DHMRW^elrv~1 1 1 1  1 1 1 1 1 RRR1 OR RRRR'R/R8RARJRSR*R]HRgRoR{ R1 LRXRR,R4R8R٬\?yX5;?sQuꕲ q-C6ho cyX5;;On鷯 rhMSt$￳ q1ZӼ8gDio' >٬\?v/@9#J{? o_y?_L?0*^I +ۿGzX$^)ec]ʡEʡE{P;pΈ :H_LJk yX5;?9#J{?zGa @Af߿ˡEvOjMd`TRMbX9sA Q6[V-~k 꿝&†#~j濅Q y)ZӼ?o_Qs o_y?Af߿n@Bi?o_?Zڊ?(ݿm4Bi䃞ͪ Qտ6>W[a4lʿd]Fx+X迎uqBQ_L?ˡEBi?z):?c=yX?&S:?ho~:pjtzG(Ciqx&1On*Dڬ\mAc]K[< u0*vOjMo_?c=yX?H.!?K7A`?&?\ Ac:M؁sFֿӼ#~jGx $(37ٿxz,C'†WPkwͪV6ho?QI&ʿY8m?(ڿz6>_Q?x $(~|?5^ٿ(?ۿXu濰rh|׿hoXsAm4~:p?㿹ٿQI&ʿ`vO*@X;Nё\V/ۿܿ48EG-C6Gz.1鷯[Ӽ_LJ c$ QBijt\ Acxz,CY8m?Xm4@@ua4lV}¿W/'˿q-hoR'jMS𿬋ho򿦛 ryX5;^)6[䃞ͪzG:M'†W(ڿ;Nё\u|гYu@J4SٿXPn俐1$}?5^IBi37;Onec]V- Qտ(؁sFֿPkwz6>V/ۿa4J4lV}.@a+e?Zd;O"uտU0*=Uۿ~k 꿅|гY٬\mտ鷯ʡE~k 6>W[CiqӼͪV_Q?ܿlV}¿Sٿa+e?N@?Zd;?cZB>詿NbX97A`вK46ܿb=yؿ rhʡE&†a4x&1#~jx $(~48EGW/'˿XZd;OZd;?"u@-C6J?c=yX?x&n4@?1%̿x鶿MSt${P#~j濋lʿOnGx $(6詿-C6J?Fx $@?߾Ŀꕲ q?y&1?HPs?;Nё\? q;pΈQd]Fx*D37Fx $(쿮Gzho忐1U0*NbX9c=yX??߾Ŀ@@0*?Cl6>W[L F%uֿ1 y)+ڬ\mW[鿴Yڊ8EGr7@;pΈ?' k QB忉 ;Nё\a+erh|׿_LJ r37٬\mտ x鶿;Nё\?L F%uֿU0*?On׿;pΈ??ܵ@$.0Zv? ?X? 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