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} EuB@$‹R A; |EE9E~EHP4$]E[^_UWVS,E @E;& }& MEM9|;};& }75& uɉUʋuR$ɍd$DA;]|S$d$ʡ& & Q& G;}~ء& @}fE fEm]mEػu؋E 9& m]mE9~;]Cm]mE9~;]~{;]tp& $Eu& ]E)& V$d$& $$$UF;u PMDd|];u , FP$d$R,$d$MAuB;U ~غ;U}M؋]B9|u؋E 9 }fE fE졸& m]mE9~;]Cm]mE9~;]~{;]u& 4Wu]u& 4Su& $ EuE ]E$V$d$& $E$EUF;u ;u MB;U ~غ;U}]؋uB9|EEe[^_UWVS } E;0}UB9}FM;1| Pþ;7+DDD F9~׾E;0}1MQD D@D@$\F;1|ω؍e[^_UWVSu];}RF9B$} $}4Z,+FB$E $)P$d$} E4Z,A;|[^_UWVSDžƅ;ƅju 蘹 $@j& $@Y& 5& x;t %u/ hS|;t%t׃Vh|P!;t h~+ WVPh|  u 5& 5& ua5& & 5& q& e[^_UWVSE & EPuDNjE$& E$& E$& E$& E$&  uhuh|u=~g5& 5& uWx yDžl@ ؉TDžlUR TEx,y@,E@,PFB$|E@uB(E@t1Džh}Džd}Dž`}Dž\}Ur0VDžh}Dž` Ex0wL@0$Džd}Dž\`@Džd}Dž\*Džd}Dž\Džd`Dž\};}KV@DI9XwDэAXXC;|X*~ DžX(X  DžXX`h ~u \h ~uPt,=t1~6~PPh@uh<~uo XPh@~xSdhh^~he~Su/ }tujjhq~ujjhz~Pt@Pt }th Pthbh6j6vHXh~xP ;yTcTtF@$UEuJTtF@(UBEu&Tt5F@,UBEtTul lV@(d$\$@$$0pxPu }t F@,d$$h~uF@0ـE@tDٽvfv ft٭t۝p٭vpPh~u2؃uj C;e[^_UWVS }u E>j7E<${8;}uVxtdWpu8y F@E<t!Fph5iEFWEC;|;}E<u GC;| Wu V}u&}t 5j$jhe$e[^_ÐUVS-19sƐC9r[^USP-Xu ]6KuUSRt ЋuX[USR[Îj] -i model_file required (or -modelfile) -db seq_file required -id seq_id optional Create .pdoc, posterior decoding of model and single sequence, either first in database file or specified with -id. %s cannot be used with viterbi scoring No database files (-db) or NLL file specified %s: No model specified. Try -insert modelfile %s: Multiple IDs are specified. Only the first one found (%s) will be used. No sequence found in database files %% Sequence %s has %d positions. %s.%s.freqFREQ08/27/04_17:45:40(October 5, 1998)2.2.1SAM: %s v%s %s compiled %s.SAM: %s v%s %s compiled %s. .pdoc%% Model File: %s %% Null Model File: %s Inserted Files: Database File: Total of %1d sequences read. SEQUENCE POSTERIORS sequence.c:add_seq_to_table() Null seqtab sequence.c:remove_seq_from_table() Null seqtab sequence.c:free_seq_data_align_from_table() ; Warning: %d letters converted to wildcard in sequence %s ; Warning: %d RNA U converted to DNA T in sequence %s ; Warning: %d DNA T converted to RNA U in sequence %s Warning: %d letters converted to wildcard in sequence %s Warning: %d RNA U converted to DNA T in sequence %s Warning: %d DNA T converted to RNA U in sequence %s sequence.c:add_control(): Not all alignments of same length print_seqalignment with null file str_w_deletions maxlen (%d) exceeded by %d on sequence %s. seq_max_stats passed null SeqInfocount_letter: letter not in alphabetSee readseq documentation (in SAM src/readseq) for more information Error (open_outputfile): Could not open file %s Empty sequence %s in %s ignored Warning: %s has only nucleotide characters and alphabet is protein. Could not open sequence weight file %s Weight file %s has an invalid Num_Sequences Num_families line or is missing a description line. Memory allocation error in read_weights %s s %d f %d Weightfile %s: too few entries; %d of %d found. No ID for sequence %d in weightfile %s Weightfile %s: Null weight for %s (%d) set to 1.0 Weightfile %s: %5.2f for %s reset to 0.0 Weightfile %s will not be used. %% %s from %s have %d families. %% Total weights: %% %s from %s. Total (%3.2f) Max (%3.2f) Min (%3.2f) No weight found for sequence ID =>%s<= setting to default weight of unity . . . sequence ID %s is listed in the weights file but not the sequence file Null weight field in sequence array. setting to default of unity . . . There is not enough room to read all the data files into memory. Please run on a machine with more virtual memory or split up the data files. No database files found. Use -db . Segment number (%d) is larger than number of segments (%d) With %d sequences and %d-sequence segments, segment %d is empty. No sequences found in database files. Segmented_read_seqfile_list passed non-empty seqtable.Unable to find sequence `%s'. ID %s selected twice; skipping repeat. No sequences specified; exiting %c SAM: Sequence Alignment and Modeling Software System %c (c) 1992-1998 Regents of the University of California, Santa Cruz %c http://www.cse.ucsc.edu/research/compbio/sam.html %c ------ Citations (HMMs, SAM) ------ %c A. Krogh et al., Hidden Markov models in computational biology: %c Applications to protein modeling, JMB 235:1501-1531, Feb 1994. %c R. Hughey, A. Krogh, Hidden Markov models for sequence analysis: %c Extension and analysis of the basic method, CABIOS 12:95-107, 1996. %% -------------------------------------------------------------- AGCTURYNAborting ,HSSP%s#%d %% Max/Min weights: %3.2f/%3.2f %% Weight Description: %s %c %s %c ----------------------- %% Run start: %s%% Run name: %s %% On host: %s %% In dir: %s %% By user: %s %% %% Total CPU time: %s %% Finished at: %sY@?original valuestraining letter frequenciesthe flat distributiontarget letter frequenciesthe generic nodeillegal method setting%s %s %s (%d). FIM_methodInsert_methodboth ends of the model. +modlenmake_freqavemodels.cfreqsumExiting program.Surgery procedure skipped. D%d-%d I%d{%d} Ignorable random_letter erroruq!>@@MbPMbP?>-C6??match frequency arithmetic meangeometric mean of match probabilitiesMake_geom_ave: no non-FIM nodes found. Invalid %s: %d (%s) specified. %s %d (%s) not available in model. Tables not modified. Error in change_inserts: no model available!! Some FIMs have non-zero match states (e.g., node %d), a natural result of turning an existing or GENERIC node into a FIM. These nodes are being renormalized as discussed in the SAM manual. To avoid this message, use addfims or hmmedit when adding FIMs. %% %% FIMs automatically added (auto_fim = %d). %% %% FIM delete removed from alignments (auto_fim = %d). %% FIM adjustments: fimstrength %4.2f fimtrans %4.2f Warning: Smith & Waterman works best with FIMs at %s%% Sequence-submodel (semilocal) (SW = %i). %% Subsequence-submodel (local) (SW = %i). %% Subsequence-model (local) (SW = %i). %% Sequence-model (global) (SW = %i). %% Warning: S&W scores are NOT adjusted. %% S&W simple NULL scores adjusted by ln(seqlen%s) (adjust_score=%d). Error in locating FIM delete in %s rmodel2model: Node %d in model length %d missing, no generic node Warning: analyse_freq computes 0 Nseq for unknown reason. %% Surgery, New mod. length %d %% /%REGULARIZERFREQUENCIESNULLMODELalphabet_def %s %s alphabet %s ENDMODEL%; %*s %d%s%s%s%s%s%s%s%s(%d): %*s%s%1sBINARYPRIOR_PATH/projects/compbio/lib%s(%d): Replacing %s with %s%s(%d): Reading %s from %s %8.6f %4d %s -- %s GENERICLETTCOUNTFREQAVETYPE %d %c BeginEnd %s BINARY %s -- %s Old modelfile is not readable New modelfile is not writable %s Too few entries in a regularizer or model node --- check alphabet (was %d should be %d for alphabet %s %s Extra characters (%s)[%d] in regularizer or model node ignored --- check alphabet (there should be %d numbers for alphabet %s). Further warnings of this type suppressed. %scomplete_line: called with bad linelength models.c:lete_line(): Have maintainer Increase LINELENGTH. %s: %s not found before end of file in model definition. Model or regularizer is missing. %s(%d): Model or regularizer is missing %s. -1 in the type specification to n, or use the addfims program.can change 'n' in the model specification to -1, change to refer to node n if nodes 1...n are declared. You SAM currently does not translate, for example, TYPE -1 (The node range is %d:%d, while type range is %d:%d past specified model nodes, without a generic mode. %s(%d): This model contains type declarations that extend Warning: %s: Node %d has two types: %c and %c. %s Missing node specifications starting at node %d (length = %d)%s: End marked as special??? Check model specification.%s `TYPE %d %c' specified but not node %d. No generic found.The %s file %s could not be read. The $PRIOR_PATH file %s could not either. No model found in the %s file %s %% %4d acc: %d env: %d code: %d <-| h㈵%4B}Error: %s exec gunzip -c exec uncompress -c Error: pclose failed: %s user %3d:%2d:%2d system %3d:%2d:%2d Error: Couldn't open file %s: %s Error: close_read: file not open Error: gzcat terminated on an error: %d AlphaChar= %d NumDistr= %d Number= %d Mixture= %f Alpha= %lf FullUpdate= %d QUpdate= %d StructID= %s Comment= %s %s/%s%% %s has AlphaChar=AlphaCharNumDistr=NumDistr =%dIgnoring prior library %s. Number=NumberMixture=MixtureAlpha=Alpha =%lf%d prior%s on %d characters. NumEnvsNumEnvs= %dAlphaChar= %dOrderEnvNumAccBinNumEnvClassesEndEnvCodingState%*s %c-----L= %dNumber= %dMixture= %lfjustDMI %s . Using single-component regularizer. Warning: Prior library %s not found in current directory or in $PRIOR_PATH %s/%sERROR: File %s does not appear to be a prior library. Prior library is for %d characters but alphabet has %d %% Prior library ignored: alphabet mismatch (%d vs %d). Error in reading prior library %s. %d components read--expecting %d. Exiting! %% The mixture coefficients summed to %lf, and were renormalized prior.c():adapt_family_frequencies unimplemented. Calling adapt_frequencies on each family individually. The number of environment transition priors read (%d) does not match the number specified(%d) in %s. Transition priors for %d environment(s) read from %s. ERROR: Don't know this environment code. {Gz? ifsssssssssssssssssstrainseedNmodelstrain2testtest2alignfiletemplatetrans_priorstransweightsequence_modelsprior_libraryprotein_priornucleotide_priorsequence_weightsalignment_weightsweight_lengthweight_finalweightmix_finalinternal_weightprint_all_weightsi_weightmix_weightsoffsetweight_normsample_trainregularizer_filenullmodel_filefamily_base_filealphabet_definsert_file_proteinpinsert_listcountinsert_file_dnadinsert_listcountinsert_file_rnarinsert_listcountreglengthrerunprint_frequenciesNseqNtrainreestimatesstopcriterionnsurgeryrandomizeanneal_lengthweightmix_lengthanneal_noiseinitial_noisesurgery_noise_scaleretrain_noise_scaleprior_weightprint_surg_modelsprint_all_modelsmany_filessequence_warningauto_fimalign_fimtrain_reset_insertsdbdblistcountididlistcountsmoothfileNLLfileNLLfile2NLLfile1allow_untiedminmodlenmaxmodlenmodellengthmodel_abort_lengthdel_jump_confmatch_jump_confinsert_jump_confins_jump_confmatchconfinsconffimstrengthfimtransmaxinsertsmainline_cutoffcutmatchcutinsertfracinsertSWSW_scorejump_in_probjump_out_probviterbiNscoreSeqcalc_smoothread_smoothwindow_sizeFIM_method_trainInsert_method_trainmdNLLnullmdNULLminusNULLmdNLLcomplexmdEmaxselect_seqselect_mdselect_scoreselect_alignselect_mdalignsortsort_scoressubtract_nullsimple_thresholdcalibrate_thresholdviterbi_thresholdadjust_scoreadpstyleMotifcutoffalignshortdbsizemultdomainshortmatrixswlambdatauquerygapcontinuehistbinsplotmaxplotminplotleftplotrightplotpsplotnegateplotlinebinary_outputsegmentssegment_numbersegment_sizea2mdotsmaxmemrecode1.20compblosum62default.paramsAborting. %s Cannot specify %s here. %s Skipping %s %s Reading %s %s Could not understand %s Reading parameter file %s Command line option%s%s %d %s%s %f %s%s %s Initial regularizerSAMRCHOME/.samrcinitial modelnull model-dump_parameters %s%sDumping parameters to file %s.params Only %d %s values can be specified. Skipping %s. %s Value not specified for %s %s%s has already been set. Using %s. %s Incorrect type or missing value for %s %s%s has already been set. Using %s. Illegal code (%d) in processes_init_entry. %s Note: Last %s specified will be used. Unkown type in init.c:print_init: %d name: %s Error: init.c:var_changed given unfound variable address. Error: init.c:mark_var_changed given unfound variable address. Error: init.c:mark_var_same given unfound variable address. %% %% Additional default parameters from SAMRC = %% %s %% Reading default parameters from SAMRC=%s %% %% Additional default parameters from %% %s/.samrc %% Reading default parameters from %s/.samrc %% %% Additional default parameters from %% %s %% Reading default parameters from %s basic_command_line called twice! exiting Please see the SAM documentation for help. Usage: %s run_name [-option value]* This program requires a SAM model specified as either -i file, while file contains a %s, or -model_file file, where file contains any model structure. This program requires a SAM regularizer specified as either -regularizer_file file, where file contains any model structure. This program requires a SAM complex null model specified as either -nullmodel_file file, where file contains any model structure. init.c: basic_command_line called with illegal required model. unalignedHSSP alignmentA2M alignmentall positions alignmentUnknown alignment type%s%d (uppercase or '-')Alignment weightsNode %d is a FIM. %s_%d:%d treating every uppercase, lowercase, period and hyphen as a column. does not have the same number of capitals and hyphens, SAM will try In a2m format, a column is a capital letter or -. If each sequence There must be the same number of columns in each sequence. File %s (%d sequences) does not look like an alignment. %s%s%s%sSAM will ignore the alignment file. On the WWW server, SAM will train a model on the unaligned sequences. Reading alignment file %s (%d sequences, %d columns) as %s. Warning: In alignment file %s, the first sequence (%s) has %d match positions%s while sequence %d (%s) has %d. Internal error reading alignment file %d %d No alignment found in alignment file %s. igstanfordgenbankgbnbrfembluwgcgdnastriderfitchpearsonfastazukerolsenphylipphylip3.2phylip3.3phylip3.4phylip-interleavedphylip-sequentialplainrawpircodataasn.1msfpaupnexusprettyUnknownABCDEFGHIKLMNPQRSTVWXYZ*ACGTUEFIPQZ %d) %s ; DNA sequence ENTRY///SEQUENCELOCUSORIGINID SQ %s(%d)[%d] Length: ..identity: Data:Name: interleavntax=nchar=matchchar=From Received:MSF:Type:Check:::=BioseqSeq-entrySeq-submit#NEXUSENTRY %d%dBioseq-set%ld%ld%30schecksumbasesLOCUS %s %ld bp ORIGIN ENTRY %s SEQUENCE %10ld>P1;%s >DL;%s %s, %ld bases, %lX checksum. ID %s SQ %ld BP ; ### from DNA Strider ;-) %-10s aanot-set seq { id { local id %d }, descr { title "%s" }, inst { seq-data iupacaa " iupacna "" } } ,%%+%ds %%%d.%ds %%%ds %%%dd %-9ld *S-S6S>SASFSMSKSQSTS\SbSjSpS vS |S S S S S S S S SSSSSSS_.-?_.-*?_.-*?<>{}[]()!@#$%^&=+;:'/|`~"\0123456789~!@#$%^&*(/Kg!Yuؚ͚=0w,aQ mjp5c飕d2yҗ+L |~-d jHqA}mQDžӃVlkdzbeO\lcc=  n;^iLA`rqgjm Zjz  ' }Dңhi]Wbgeq6lknv+ӉZzJgo߹ﾎCՎ`~ѡ8ROggW?K6H+ L J6`zA`Ugn1yiFafo%6hRw G "/&U;( Z+j\1е,[d&c윣ju m ?6grWJz+{8 Ғ |! ӆBhn[&wowGZpj;f\ eibkaElx TN³9a&g`MGiIwn>JjѮZf @;7SŞϲG0򽽊º0S$6к)WTg#.zfJah]+o*7 Z-I$jее۲۲k,)KeIPW^DEFINITION %s, %ld bases, %lX checksum. TITLE %s, %ld bases, %lX checksum. DE %s, %ld bases, %lX checksum. %s Length: %ld (today) Check: %ld .. ; DNA sequence %s, %ld bases, %lX checksum. ; repr raw, mol %s, length %ld, topology linear, [Name: %-16s Len:%6ld Check: %8lX] Name: %-16s Len:%6ld Check: %8lX Name: %-16s Len:%6ld Check: %5ld Weight: 1.00 ;%s, %ld bases, %lX checksum. >%s, %ld bases, %lX checksum. 1. IG/Stanford 2. GenBank/GB 3. NBRF 4. EMBL 5. GCG 6. DNAStrider 7. Fitch 8. Pearson/Fasta 9. Zuker (in-only)10. Olsen (in-only)11. Phylip3.212. Phylip13. Plain/Raw14. PIR/CODATA15. MSF16. ASN.117. PAUP/NEXUS18. Pretty (out-only)(unknown)ReadSeq (file %s): File not found ReadSeq (file %s): Can't open output file. ReadSeq (file %s): Error in ASN.1 sequence routines. ReadSeq (file %s): No data in file. ReadSeq (file %s): Specified item not in file. ReadSeq (file %s): This format requires equal length sequences. Sequence truncated or padded to fit. ReadSeq (file %s): Error: this format is unknown to me. ReadSeq (file %s): Warning: This format permits only 1 sequence per file. ReadSeq (file %s): Out of storage memory. Sequence truncated. ReadSeq (file %s): readSeq error = %d 8d-YoNzC"HHHEEETTT*HHHH**EEEE*TT**TT**HH****EE****TT*****TEMPLATESEQLENGTH%*s %s %c %c %dNALIGN## ALIGNMENTS%*s %*s %d - %dAASTRUCTACC%s, %d%s.tplatecan not open "%s": %s TEMPLATE %% File generated %s%% %% SEQLENGTH %d ID %s %% %% %c %c %d Warning: Template file %s could not be read ERROR: The specified template file is not a template file. Program execution is unpredictable. ERROR: Number of residues read from templatesequence does not match number specified infile. Or, no sequences found. %% %% %% Template sequence from %s %% %%AA STRUCTURE ACCESSIBILITY %%-- ----------- ------------- null_mod_score: new, long alphabet encountered. No model in select_simple_null_node Warning: First model node is not a FIM but null model probabilities are being taken from it Bad value for subtract_null (%d), using SIMPLE (%d) Warning: user null selected (subtract_null = %d), but no null model (%s-type model) found. Using simple null model. Database has %d sequences with %1.0f residues. %% %d sequences with %1.0f residues. %% The model has %d positions. %% %% Using total residues as number of starting possibilities, %% 0.01 significance at <= ln(0.01)-ln(%d)= -4.6 - %4.1f = %-5.1f %% Adjusting for model length gives %d starting points, %% 0.01 significance at <= ln(0.01)-ln(%d) = -4.6 - %4.1f = %-5.1f %% If entire sequences are modeled (i.e., no FIMs), %% Values for 10.0 significance are %5.1f, %5.1f, and %5.1f. %% Significance level is higher for multiple scoring runs. Null node in null_mod_score anyway. posterior decoding posterior decoded alignmentEM%% This run used %s scoring. Model FIM_method_scoreModel Insert_method_scoreffffffffffff@zD?n: %d%s%s %s %s %s %s %s %s%s%sMin:%s %s Max:%s %s Ave:%s SampDev:%s %s%s@.weightoutputcandidate model #%d %% %d sequences and families family %d %d ID Weight NLL-null Score %s %f DNAAGCTRYNRNAAGCURYNACDEFGHIKLMNPQRSTVWYBZX%s %sprocess_alphabetalphabet.cdefidx >= 0Legal alphabets are: alphabet_id_to_info: unknown alphabet id %d Error: alphabet is %s, trying to set it to %s. No sequence file found to set alphabet. Trying %s. No alphabet specified and file %s no help. Trying %s alphabet_def should be in the form "name letters"; got "%s"Error: alphabet is %s, is defined as "%s" trying to set it to "%s". minimum defined alphabet is two letters plus a wild character alphabet can only contain alphabetic characters, got "%s" Unrecognized alphabet %s in init file, %s used. Length of alphabet %s exceeds MAX_ALPHA_LENGTH Insufficient memory for posdecode values (modlength=%d seqlength=%d) Insufficient memory in PDmodel creationNull model or modweight in model2fbmodel init_forward2 called with null model! Illegal SW option (%d). Current options are Global (%d), semi-local (%d), local (%d), and domain (%d) forward2 is receiving a model of length %d?? Warning: A dynamic programming matrix of %d KB is being allocated even though maxmem is only %d (%d KB) Unable to allocate %d bytes with maxmem %d, model length %d, and sequence length %d .Reduce maxmem to zero for minimal memory usage by putting '-maxmem 0' on the command line. Reduce sequence length and especially modellength to enable SAM to fit in malloc-able memory. Insufficient memory for PDalign (ml=%d,sl=%d) Error in forward2:encode_algnment Internal error in encode_alignment init_forward2 must be called before forward_score init_forward2 must be called before forward2 Not enough space: Increase maxmem Internal traceback error. Exiting. Try larger maxmem. A value of %d will be used Not enough memoryforward2.c: unknown alphabetResidue %d %f (Char %c, index %d) combine_rows_posdecodeforward2.cPD != ((void *)0)encode_alignmentalign[i] < 0@ 1Creates .plt, a gnuplot plot file, and .data file(s), the data for the curve(s). To use, start up gnuplot and enter the command 'load ".plt"'. Plot options: Not all are used in all plotting programs. [-plotmax ] Highest Y axis value [-plotmin ] Lowest Y axis value Y axis calculated internally if plotmax = plotmin [-plotleft ] Lowest X axis value [-plotright ] Highest X axis value X axis calculated internally if plotleft = plotright [-plotline ] Vertical line at plotline if <> 0 [-plotnegate <0/1>] Negate scores if 1 [-plotps <0/1/2>] Create ".ps" (1) If plotps=2, a square plot is generated. set arrow from %f,%f to %f,%f nohead Error in gnuplot: temporary files not deleted. # Uncomment the next two lines to generate a postscript file. %sset terminal postscript eps %5.2f %d %5.2f %5.2f set yrange [%f:%f] set xrange [%f:%f] gnuplot %s.plt#%sset output "%s.ps" %sset size 0.7, 1.0 set title "%s %s" set xlabel "%s" set ylabel "%s" set nozeroaxis $@.A%*s%f%d%f%f%% Number of outliers: %1d SLOPE %f %d %f %f Reading scores from file %s %s%d%f%f%f%% %s %s%s: All betterworse%% %s %s%s%sif %s than: %% C1/Simple (%6.3f) C2/Complex (%6.3f) Zscore (%6.3f) All (%s=%d) Column1Column2the first column of scoresthe second column of scoresSimpleComplexUser'sReversethe raw NLL score%% %% Column 1: %s %% Column 2: %s bestworst%% %%%% %%-%ds %%6s %%11s %%11sLengthSequence ID Z-score X count %%-%ds %%5d %%11.2f %%11.2f%10.3f %3d XFile containing smoothed data is out of order%% Smooth curve from file: %s Warning: mdNLLnull (%f) is greater than zero. With NLL-NULL scoring, negative numbers indicate similarity. Multdomain may crash with this value. Error: %s = 4 (Zmax), but no Zscores are available. NLL-NULL using simple FIM (node 0) insert probabilitiesComplex model NLL-NULL score using FIM (or node 0) probabilitiesNLL-NULL for user input NULL modelNLL-NULL for the reverse sequence NULL model%% Scores sorted by column %d, %s first No sequences specified; exiting mss ܈܈ƈ <Rl '  H(  )  (( 4' 9( >( ڽ' FT) M ' R& X' b0( kd( x' L) ' ' ( 8' ҹ' & & ' ' <' 1' :,) FP( M' Y' {T' f@( wD) `' WX( ۺl' X( ۺl'  Zv,'  _,'  ' X) ' ʺ& ں' ( ' 4( H) ' 0' 5 ( <,( H$( V' _( iL( wP) ( & 8) t' ˻' ػ\( ' 8(  ) `)  ' *@' H'  >$' A'  M`( P<) \X' g' o0' x' T( ' ' 4) ( \' ϼ& ߼D( D( @) d' & <( %P' 0() @p' Ih' SD' ^& a& j\) w' ' ' ' x' $) 0)  ( ̽(' ( ( ( ( (  ( ( ( ( #( 0( =( L( Q( ]( k( |( ( k( l( ( ( ( ľ( Ͼ( ־( ( ( ( ( ( ( (  ' ) ' &' /L' 9' @' K|' T' b' k ' z4' ' '  STTW__o_~__________``!`)`3`B`ntcxc|cccccccccccccc-m1m?> >?iWxAp@-g>,>5@>>>>>>>>9m=m?> >?iWxAp@-g>,>5@>>>>>>>>Em?> >?iWxAp@-g>,>5@7q= =?=J="=)y= ==Ҥ=9Ѯ=q<%=ՕO==†'==o=닄=@+<<7q= =?=J="=)y= ==Ҥ=9Ѯ=q<%=ՕO==†'==o=닄=@+<< ?DMIXJ  (||  @`Ho؋oo8īΎގ.>N^n~Ώޏ.>N^n~ΐސ.>N^n~Αޑ.>N^n~Βޒ.>GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)GCC: (GNU) 3.2.2 20030222 (Red Hat Linux 3.2.2-5)H$,$  l#$ &!_IO_stdin_usedHl../sysdeps/i386/elf/start.S/usr/src/build/324954-i386/BUILD/glibc-2.3.2-200304020432/csuGNU AS 2.13.90.0.18oll/<<#LSLfintN b VLb {MfLO|IS#NZ#  # O#7:# _:!#"#2 &  F  Q %    h  8  @B |XAj# ]k# e=l#m# nO#SSSd  jՅYd<?u[#va#xS#^zl#  {l# RHr}# Ki~# AN# O6# jS#$S#(S#,S#0S#4#8j$@S##S#US# S#&##@O# G=SCOUgxSSd SSbSSSS+G#CS#+#:jL_,492#3j#~,5 9/ 4: " r# $ %a ( H) *  + 7,S - G2: 3\ 9: : * s  > u   jS %  M ]    g -S  S S S e Z :   6 K S  % l \S ; E u q#  #aSa  a d!6S6a }G R5_ 7 8S 9 :DS:/usr/src/build/324954-i386/BUILD/glibc-2.3.2-200304020432/build-i386-linux/csu/crti.S/usr/src/build/324954-i386/BUILD/glibc-2.3.2-200304020432/csuGNU AS 2.13.90.0.18(/usr/src/build/324954-i386/BUILD/glibc-2.3.2-200304020432/build-i386-linux/csu/crtn.S/usr/src/build/324954-i386/BUILD/glibc-2.3.2-200304020432/csuGNU AS 2.13.90.0.18%%  : ;  : ; I8 I!I/ $ > $ >  : ; : ;I : ; I : ; I  : ; (  : ;  I' II &I' < !I4: ; I? 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Tm aґkԑwؑ y / ܑ (2 ?| S$Z(cm ; |,2 { W &Y  b % ' s)7 )  *k , /- 1=4I8U1 eb3 r5 y&<@` cU U \ @xe x VP$~> -E 5`% ?| F4 O5d W `r f  m0 x V &  V b :O   - ·V $  /  ԉf :  ϋT "# * >ē Q g4 {E B( `L@|   . ?Jo ^sG nEX {(P \t ,48<@DH L P T X \! `* d1 h; lE pT tc xn |~      v m* ~  L e   mH     - 6 = H Q X & i & w )& P Q #V Y Z+ [ $`Y  q;  ! + |s# : s H sM R tY Y `t/ h u t vJ { &  &  &  &  Zy "zl &  &   * 6, b, N  g  J+  U   , & 5   A ], a & m  n &   r% tk A &   6 ԡ  &  & ! jL + & 9  N Ea_ a & q ' x ȎY,  ؎m UD څ  g Z  X R 'm7 ?' I' U ' cT4Z ml ' m  ī<S w a}h Ez q %(:& G8 W0]' lr y~ ' + n1) ' %  ' 82c H%$' 6 ('  %,' 2@98 N0' [0 d4' pX#h  xC1 M6  && 8'  * 0$ D|q P& f6x}3    <'  @' DF 2  $D' /I <u{ C@ ] nB {; 3q ȏJ_ đ H' L' [ 4 !P' ,_i DT' S'`D aX' pX xW\' / `' d' h'  ;@ l' 7> ؏ |M V7 $B C? UW d t| p' t' p '  ~ {W@ s x' :1  :|' Cd) Ka]4 j p(7'  j2 86 %1 ' H#'  ' k` )' 8 AXR' Z' f5 plv j4 .9 ' ' ? ' |( A '  ܀F W)w} 5GYJ nh . P '  ' ' s ٣D ' ' %{I 9' D} Sg_8 hlR s' =1   ' -6  J x] D8 '  q B 1' C@STx _' nAx H SH &$ ' S 0 &F' | *' @ȐR9 _' h}e v  1i ' dq Ģ#  ' "  < _D ' (' 5ؐR}x ^Uo' ~-$f     g ' l HW ' @ B- ' &W 1~D >. Pb( g v zk [/ ( A~F L(   ( Y !] + X 3( @Sd0 t= ( jc TNQ (  ح{ (  ɯo ,K_ % ( ,$( :" J! ZQ# h(+4 . m 2  CD (( 8X/ ({ <+ EHXXjB {47 ,( @ rm  h0f  p οi   x'" K 3 F < 0( E _D Q ' _ q q  nB 6 ȑ 'F 4(  ؑW! !t !!p .!8( 9!1% ?! K! 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