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Bad format?No. of seqs=%dNo. of seqs in profile=%dTotal no. of seqs =%dSequences assumed to be %sbpaaSequence %d: %-*s %6.d %s Sequences should all be in 1 file. 7 formats accepted: NBRF/PIR, EMBL/SwissProt, Pearson (Fasta), GDE, Clustal, GCG/MSF, RSF. Output file name is the same as input file.wCannot open output file [%s]Bad output file [%s]You must select an alignment output formataln Enter a name for the CLUSTAL output file Enter a name for the NBRF/PIR output filemsf Enter a name for the GCG output file phy Enter a name for the PHYLIP output file Enter a name for the GDE output file nxs Enter a name for the NEXUS output file PileUp MSF:%5d Type: Check:%6ld .. Name: %s oo Len:%5d Check:%6ld Weight: %.1f // #NEXUS BEGIN DATA; dimensions ntax=%d nchar=%d; format missing=? symbols="" interleave datatype=DNA PROTEIN gap= -; matrix; end; 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.%6d %6d %-10s >DL;>P1;%s %s * Enter a name for the parameter output file [%s]: 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 No sequences in memory. Load sequences first.Less than 2 sequences in memory. Phylogenetic tree cannot be built.Start of Pairwise alignmentsdnd Enter name for new GUIDE TREE file Guide tree file created: [%s]#%%%s "SS_%-*s "GM_%-*s CLUSTAL %s multiple sequence alignment !SS_%-*s %s !GM_%-*s %s %-*s %s %dConsensus length = %dCLUSTAL-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 guide tree file [%s]: Cannot open 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 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]: Cannot open help file [%s]No help found in help file>>HELP0123456789ABCDEFGHIJKLMNOPQRSTUVWXYZ Unknown SCORE type: %s Bad option for /seed (must be integer) temp = %d; seed = %u; Unknown OUTPUT type: %s 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) idBad option for /maxdiv (must be integer) Bad option for /gapdist (must be integer) Bad option for /debug (must be integer) Unknown case %s Unknown SEQNO option %s %fBad 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 Unknown bootlabels 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) CLUSTAL %s Multiple Sequence Alignments Error: too many command line arguments Error: parameter required for /%s Error: unknown option %c%s clustalw option list:- %c%s%s=%s OR %sSequence type explicitly set to ProteinSequence type explicitly set to DNA Unknown sequence type %s Bad sequence file name No. of seqs. read = %d. No alignment! Bad profile 1 file nameBad profile 2 file nameOnly 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 fileInvalid option /usetree1.Cannot align profiles. No tree file specifiedInvalid option /newtree1.Invalid option /usetree2.Invalid option /newtree2.No input file(s) specifiedABCDEFGHIKLMNPQRSTUVWXYZ-unknownEMBL/Swiss-ProtPIRPearsonGDEClustalPileup/MSFRSFUSERPHYLIPNEXUSIDFT%sHELIXSTRANDUse it to set local gap penalties %s%d%dGM%d%d%dSQCLUSTALPILEUP!!AA_MULTIPLE_ALIGNMENT!!NA_MULTIPLE_ALIGNMENTMSF!!RICH_SEQUENCE#NEXUSPIR format sequence end marker '*' missing for one or more sequences.PIR format sequence end marker '*' missing for one or more sequences.//SS_GM_namesequenceEnter the name of the sequence filerCould not open sequence file %sSequence format is %sCannot read nexus format%s%sACGTUNMultiple sequences found with same name, %s (first %d chars are significant)!SS!GMbad secondary structure formatbad gap penalty mask formatfeature%d%d%d%s%s%s (Partial alignment)Sequences (%d:%d) Aligned. Score: %lgSequences (%d:%d) Not AlignedStart of Multiple AlignmentThere are %d groupsAligning...Group %d: Sequences:%4d Score:%dGroup %d: DelayedSequence:%d Score:%dsequence %d: %d new weights Start of Initial AlignmentSequences:%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 command%d of the distances out of a total of %d Neighbor-joining Method Saitou, N. and Nei, M. (1987) The Neighbor-joining Method: A New Method for Reconstructing Phylogenetic Trees. Mol. Biol. Evol., 4(4), 406-425 This is an UNROOTED tree Numbers in parentheses are branch lengths Cycle 1 = SEQ: 1 (%9.5f) joins SEQ: 2 (%9.5f) Cycle%4d = Node:%4d (%9.5f) joins SEQ:%4d (%9.5f) joins Node:%4d (%9.5f) SEQ:%4d (%9.5f) Cycle%4d (Last cycle, trichotomy): Node:%4d (%9.5f) SEQ:%4d (%9.5f) joins%6d %-*s %6.3f %7d%1d:%7.5f,:%7.5f[%d]%d:%7.5f)#NEXUS BEGIN TREES; TRANSLATE %d %s, %d %s ; UTREE PAUP_1= (%d:%7.5f,%d:%7.5f);TRICHOTOMY ENDBLOCK; ( :%7.5f, , ) %.*s:%7.5f) (%s:%7.5f,%s:%7.5f);; ACGTU DIST = percentage divergence (/100) Length = number of sites used in comparison All sites with gaps (in any sequence) deleted Distances up tp 0.75 corrected by Kimura's empirical method: Kimura, M. (1983) The Neutral Theory of Molecular Evolution. Page 75. Cambridge University Press, Cambridge, England.%4d vs.%4d DIST = %6.4f; length = %6.0f p = rate of transition (A <-> G; C <-> T) q = rate of transversion All sites with gaps (in any sequence) deleted! Distances corrected by Kimura's 2 parameter model: Kimura, M. (1980) A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J. Mol. Evol., 16, 111-120. WARNING: sequences %d and %d are non-overlapping %4d vs.%4d: DIST = %7.4f; p = %6.4f; q = %6.4f; length = %6.0f You must load an alignment firstAlignment has only %d sequencesYou must select either clustal or phylip or nexus tree output formatnjb Enter name for bootstrap output file phbtreb 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; defining 2 groups. Each column is 1 sequence; the stars in each line show 1 group; the dots show the other Numbers show occurences in bootstrap samples. Each dot represents 10 trials WARNING: %ld of the distances out of a total of %ld times %ld were out of range for the distance correction. 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] Enter name for CLUSTAL tree output file ph Enter name for PHYLIP tree output file dst Enter name for distance matrix output file tre Enter name for NEXUS tree output file Phylogenetic tree file created: [%s]Distance matrix file created: [%s]Nexus tree file created: [%s](%s:%0.5f,%s:%0.5f); A %d B %d M %d N %d midi %d go1 %d go2 %d Type 1,1: midj %d Type 1,2: midj %d Type 2,1: midj %d Type 2,2: midj %d mean tmat %3.1f sequences profile 1: sequences profile 2: iubclustalw%d %d logmin %f logdiff %f pamgonnet 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.pcid %d matrix %d pcid %3.1f scale %3.1f Error: matrix %s not found matavscore %d Gap Open1 %d Gap Open2 %d Gap Extend1 %d Gap Extend2 %d Matrix %s %c %d %d %d Error in aln_path matrix %s blosummat_avscore %d %d %d go %d ge %d %f %d %d Sequences (%d:%d) Aligned. Score: %d CompScore: %d Sequences (%d:%d) Aligned. Score: %dUsing variable zones to set gap penalties (pcid = %d) gap open %d gap ext %d gaps: gap_pos: Opening penalties: %d:%d Extension penalties: %d:%d cannot open %sWrong format in tree file %stree 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 found %s and %s (distance %1.3f) SUGGESTION: Remove one or more problem sequences and try againContinue ABCDGHKMNRSTUVWXYABCDEFGHIKLMNPQRSTVWXYZresidue %c in matrices.h is not recognisednucleic acid %c in matrices.h is not recognisedmaxres %d average mismatch score %d average match score %d average score %d min %d max %d comparison matrix not specifiedCLUSTAL_SERIESin %s - single matrix expected.too many entries in matrix %swrong format in matrix %sresidue %c in matrix %s not recognisedMATRIX%d %d %sBad format in file %s in file %s: lower limit is greater than upper (%d-%d) Bad format in matrix file %s Error: matrix blosum30 not found Alignment Score %dSecondary StructureGap Penalty MaskStructure and Penalty MaskNone %s ERROR: FATAL ERROR: WARNING: .. Interrupt Error: signal ****** Format of Phylogenetic Tree Output ****** OFFON 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 NODE LABELSBRANCH LABELS 5. Toggle Phylip bootstrap positions = %s H. HELP Enter number (or [RETURN] to exit) Unrecognised Command ****** PHYLOGENETIC TREE MENU ****** 1. Input an alignment 2. Exclude positions with gaps? = ON = OFF 3. Correct for multiple substitutions? 4. Draw tree now 5. Bootstrap tree 6. Output format options S. Execute a system command H. HELP or press [RETURN] to go back to main menu Your choice ********* SECONDARY STRUCTURE OPTIONS ********* 1. Use profile 1 secondary structure / penalty mask = YES = NO 2. Use profile 2 secondary structure / penalty mask 3. Output in alignment = %s 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 ********* Secondary Structure Output Menu ********* 1. %s 2. %s 3. %s 4. %s H. HELP -- Current output is %s -- Enter number (or [RETURN] to exit)Helix Penalty Currently: %d Enter numberStrand 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 ********* 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 UPPERLOWER 7. Toggle GDE output case = %s 8. Toggle CLUSTALW sequence numbers = %s INPUT FILEALIGNED 9. Toggle output order = %s 0. Create alignment output file(s) now? T. Toggle parameter output = %s No sequences loaded ********* 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 ********* %d. %s -- Current matrix is the %s (file = %s) ********* 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 Gap Extension Penalty Currently: %4.2f Min Identity Currently: %d Transition Weight Currently: %1.2f PROTEINDNA ********* 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 = FAST = SLOW Gap Open Penalty Currently: %4.2f Gap Penalty Currently: %d K-tuple Currently: %d Top diagonals Currently: %d Window size Currently: %d ****** PROFILE AND STRUCTURE ALIGNMENT MENU ****** 1. Input 1st. profile (loaded) 2. Input 2nd. profile/sequences 3. Align 2nd. profile to 1st. profile Slow/AccurateFast/Approximate 4. Align sequences to 1st. profile (%s) SLOWFAST 5. Toggle Slow/Fast pairwise alignments = %s 6. Pairwise alignment parameters 7. Multiple alignment parameters 8. Toggle screen display = %s 9. Output format options 0. Secondary structure options ****** 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? = ON = OFF 8. Toggle screen display = %s ************************************************************** ******** CLUSTAL %s Multiple Sequence Alignments ******** 1. Sequence Input From Disc 2. Multiple Alignments 3. Profile / Structure Alignments 4. Phylogenetic trees S. Execute a system command H. HELP X. EXIT (leave program) clustalw_helpY@@@333333??Y?@i@?-C6?ư>?(\?$@p@ @??T@N@D@>@4@A@9@{Gz??@?B?? ABLOSUM 30blosumPAM 350pamGonnet 250gonnetIdentity matrixidUser definedBLOSUM seriesblosumPAM seriespamGonnet seriesgonnetIdentity matrixidUser definedIUBiubCLUSTALW(1.6)clustalwUser definededef ff|fx%ft/f7f>f Ff4Mf0Tf,[f(hfofwfffffHfLf<f@fPfXfTfDf8fffpflggg`g\%g/g9gpCgLgVg^gjguggg(gggg(gg(gg(gg(gggg(ggggg(gg(h h(hh(h$h*h2h8h@hHhQhZhchlhvh{hhhhh(h hh(hhhhhhhhhhhhhhii iiiio?iubgonnet= A@pAGPSNDQEKRiubgonnetL> A@pAii!i%i.i(~~~%).5@   !#$&(*+-/13579;=?ACEHJLOQSVX[]`behjmpsvy| !)09AJS]gr}3Mj?TENX5_714d[i3XX9obK~_aFZ<znk[}|QjXWWhEPdhDOG~]|oKdMACDEFGHKILMNPQRSTVYW2 | ]33!   8      #|*'9h%<:- ! !  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