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HX8!P|N |!PB|vx|#x|+x:9;; |@0;W+:|kH.Ha|@|xx;9|A؀@,A 9:D,A 9:; |@0;W+:|kH.H|@|px;9|A؀4,A9,A:,,A9,A:0,A9,A:; |@0;W+:|kH.Hm|@|px;9|A|||r<8cfT88=K8U|zx<8cf`88~ƳxH; ||@0{xW):~óx<8cd|X.H;9||A؀|,@8` ~ijxH),A~óx<8ftHU$,A~óx<8fH9 ,A~óx<8fH(,A~óx<8fHh,ADl,A8;P[T~óx<8f!PPTAPPTHH0h,A$;P~óx<8f!PPTHp,ADt,A8;X[\~óx<8f!PPTAPPTHAH0p,A$;X~óx<8f!PPTH`,ADd,A8;H[L~óx<8g !PPTAPPTHH0`,A$;H~óx<8g$!PPTH; |@8[W):{~óx<8g8|P.|X.He;9|A8` ~ijxHp Ah; |@L[W+:;|+L.~óx<8gHxx|P.!PP!TH;9|A8` ~ijxH8,Ad; |@H;8W+:} H.,A$;~óx<8g`xx|H.H;9|A8` ~ijxH%<,Ad; |@H;:|H.Cx|"~xH~Z;~óx<8g~ex~fx|H.HxH;@, AH|H.,A<Cx|~xH5~Z;~óx<8gxx|H.HxHe;D, ALW>:|H.,A<Cx|~xH~Z;~óx<8gxx|H.HxH;|@tW<::;W:}=H.|H.,ADCx|~xHy~;{~óx<8gxx|H.}X.IxH;|A;9|A,,A<Cx|~xH }~óx<8g~%x~&x<8hHxH=0,A<Cx|~xH}~óx<8g~%x~&x<8hHxH4,A<Cx|~xH}~óx<8g~%x~&x<8DHxH;|@`; ;W:|H.Cx|"~xH):;~óx<8gxx|H.HxHY;|A~ |A<8c788~ƳxHECxH 8!|N |!B||x@8a@<8/<8K48,A8a@<8/<8K48|}yA8a@<8$x8K4m8|~yA|uA0, A , @ |uA, A, Ax<8^8H=,@x8K4|H<x<8 8H ,@x8K4a|$H x<8^8H,@x8K41| Hx<8^8H,@x8K4|(Hx<8^8H},@p@8a@<8/<8K358|~yApxH <P;h8a@<8/<8K2,A8H <TlH$x<8^8H ,@p@8a@<8/<8K28|~yAxH y <X;p8a@<8/<8K2u,AH I <\tHx<8^8H m,@p@8a@<8/<8K2%8|~yA`xH <H;`8a@<8/<8K1,A(H <LdHxxxK8|xh8!`|N |a!B|{x@8a@<8,8K1q8,At8a@<8,8K1Q8|}yAT8a@<8,8K118||yA48a@<8!<8K18|~yA|uA0, A , @ |uA, A, A耻cxx8K|}x{x<8[8H ,@,W:xH e |=.`Hxx<88H ,@cxxxKiHHx<8[8H Q,@cxxxKHcxxxxKA8|xx8!p|aN |!B||x@8a@<8*88K/8,A8a@<8*88K/8|~yA8a@<8*88DK/i8|}yAx<8Y8H q,@ 8|,HHx<8Y8H M,@ 8|0H$x<8688H ),@8|48xDK-HxxxK8|xh8!`|N |a!B||x@8a@<8)8K.8,A8a@<8)8K.a8|}yA8a@<8)8K.A8|~yA8a@<8)8DK.!8|{yAxxK!|}x|x<8X8H ,@@,@t<8cV81T:K)U|@<8cV82T:K)9|9@| @,9<@UK:} I.<} I.9J| AW:|@<|}|H.exDK,]<Hx<8X8HQ,@D,@t<8cV8?T:K(|D<8cV8@T:K(y|9@| @,9<DUK:} I.<} I.9J| AW:|D<|}|H.exDK+<|}I.HxxxfxK8|xx8!p|aN |!B|~x8@, @8@H$8a@<88K+8|dyAxKY8|xh8!`|N |!B|~x@8a@<8& 8K+8|}yAh8a@<8& 8DK+q8||yAHxx8Km~T}:~>|}|H.xDK*E>|}I.8|xh8!`|N px!Aaځڡ!AaہۡN px!Aaʁʡ!Aaˁˡ|N 9`@~9`P~9``~9`p~9` 9`+9`K9`k9`9`9`9`N 9`@~9`P~9``~9`p~9` 9`+9`K9`k9`9`9`9`N 9`@~9`P~9``~9`p~9` 9`+9`K9`k9`9`9`9`}`BN 9`@~9`P~9``~9`p~9` 9`+9`K9`k9`9`9`9`}@CN |B}h=k|n}9knN |B}h=k|nh}9knhN |B}h=k|nH}9knHN |B}h=k|n(}9kn(N |B}h=k|n}9knN |B}h=k|m}9kmN |B}h=k|m}9kmN |B}h=k|m}9kmN |B}h=k|m}9kmN |B}h=k|mh}9kmhN |B}h=k|mH}9kmHN |B}h=k|m(}9km(N |B}h=k|m}9kmN |B}h=k|l}9klN |B}h=k|l}9klN |B}h=k|l}9klN |B}h=k|l}9klN |B}h=k|lh}9klhN |B}h=k|lH}9klHN |B}h=k|l(}9kl(N |B}h=k|l}9klN |B}h=k|k}9kkN |B}h=k|k}9kkN |B}h=k|k}9kkN |B}h=k|k}9kkN |B}h=k|kh}9kkhN |B}h=k|kH}9kkHN |B}h=k|k(}9kk(N |B}h=k|k}9kkN |B}h=k|j}9kjN |B}h=k|j}9kjN |B}h=k|j}9kjN |B}h=k|j}9kjN |B}h=k|jh}9kjhN |B}h=k|jH}9kjHN |B}h=k|j(}9kj(N |B}h=k|j}9kjN |B}h=k|i}9kiN |B}h=k|i}9kiN |B}h=k|i}9kiN |B}h=k|i}9kiN |B}h=k|ih}9kihN |B}h=k|iH}9kiHN |B}h=k|i(}9ki(N |B}h=k|i}9kiN |B}h=k|h}9khN |B}h=k|h}9khN |B}h=k|h}9khN |B}h=k|h}9khN |B}h=k|hh}9khhN |B}h=k|hH}9khHN |B}h=k|h(}9kh(N |B}h=k|h}9khN |B}h=k|g}9kgN |B}h=k|g}9kgN |B}h=k|g}9kgN |B}h=k|g}9kgN |B}h=k|gh}9kghN |B}h=k|gH}9kgHN |B}h=k|g(}9kg(N |B}h=k|g}9kgN |B}h=k|f}9kfN |B}h=k|f}9kfN |B}h=k|f}9kfN |B}h=k|f}9kfN |B}h=k|fh}9kfhN |B}h=k|fH}9kfHN |B}h=k|f(}9kf(N |B}h=k|f}9kfN |B}h=k|e}9keN |B}h=k|e}9keN |B}h=k|e}9keN |B}h=k|e}9keN |B}h=k|eh}9kehN |B}h=k|eH}9keHN |B}h=k|e(}9ke(N |B}h=k|e}9keN |B}h=k|d}9kdN |B}h=k|d}9kdN |B}h=k|d}9kdN |B}h=k|d}9kdN |B}h=k|dh}9kdhN |B}h=k|dH}9kdHN |B}h=k|d(}9kd(N |B}h=k|d}9kdN |B}h=k|c}9kcN __dyld_mod_term_funcs__dyld_make_delayed_module_initializer_callsThe kernel support for the dynamic linker is not present to run this program. -h-n-A-E-T-Z--acc--compat--cpu--cut_ga--cut_nc--cut_tc--domE--domT--forward--informat--null2--pvm--xnuunrecognized sequence file format "%s"Incorrect number of arguments. %s PVM support is not compiled into HMMER; --pvm doesn't work.Posix threads support is not compiled into HMMER; --cpu doesn't have any effect^.*\.gz$-You can't use -n and --xnu together: I can't xnu DNA data.Failed to open sequence file %s %s HMMERDBFailed to open HMM database %s %sHMM file: %s Sequence file: %s PVM: ACTIVE- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -Query: %s %s Query sequence: %s [none]Accession: %s Description: %s Scores for sequence family classification (score includes all domains):%-*s %-*s %7s %10s %3s ModelDescriptionScoreE-value N ----------------------------------hmmpfam.c%-*s %-*.*s %7.1f %10.2g %3d [no hits above thresholds] Parsed for domains:score%-*s %7s %5s %5s %5s %5s %7s %8s Domain seq-fseq-thmm-fhmm-t%-*s %3d/%-3d %5d %5d %c%c %5d %5d %c%c %7.1f %8.2g Alignments of top-scoring domains:%s: domain %d of %d, from %d to %d: score %.1f, E = %.2g [output cut off at A = %d top alignments] //HMM file %s may be corrupt or in incorrect format; parse failedHMM %s did not contain the GA, TC, or NC cutoffs you neededno PVM supportpthread_mutex_init FAILED; %s Failed to create thread %d; return code %d pthread_join failedpthread_mutex_lock failure: %s pthread_mutex_unlock failure: %s HMM %s did not have the right GA, NC, or TC cutoffsNo such alphabet typeLooks like nucleic acid sequence, hope that's rightLooks like amino acid sequence, hope that's rightSorry, I can't tell if that's protein or DNApthread_mutex_lock FAILED: %s An alphabet type conflict occurred. You probably mixed a DNA seq file with a protein model, or vice versa.ACDEFGHIKLMNPQRSTVWYUBZXSNDQEACDEFGHIKLMNPQRSTVWYACGTUNRYMKSWHBVDXTACGTAGCTACGTCGATACTCGTACGAGTNo support for non-nucleic or protein alphabetsalphabet.ccore_algorithms.cTraceback failed.traceback failedBogus state %syou can't init get_wee_midpt with a %s HMMER: Bad state (%s) in ShadowTrace() TraceDecompose() screwupNBMDIEJCBOGUSnucleic acidunknownprotein [ trace is NULL ] st node rpos - traceback len %d -- ---- ------ %1s %4d %6d oi, you can't print scores from that hmm, it's not ready.st node rpos transit emission - traceback len %d -- ---- ------ ------- -------- %1s %4d %6d %7d %8d %c %8s %c ------- -------- total: %6d Dirichlet PAM No such strategy.Amino Nucleic %d %.4f %.4f unknown state * %c N M%-3d I%-3d E C J B D%-3d %- #11.3eM%dD%dI%dbad transition%d %s %d %s %-14.7g emit.cnever happenscan't happen.Profile %s will have more than 1000 positions. GCG won't read it; Compugen will.!!AA_PROFILE 1.0 !!NA_PROFILE 1.0 No support for profiles with non-biological alphabets(Peptide) (Nucleotide) HMMCONVERT v%s Length: %d %s|%s|%s 2.3.2 Profile converted from a profile HMM using HMMER v%s emulation. Compugen XSW extended profile format. Use -model=xsw.model -nonor -noave -gapop=10 -gapext=1 -qgapop=10 -qgapext=1 with om on the Compugen BIC to get the closest approximation to HMMER bit scores. Use -nonor -noave -gap=10 -len=1 with profilesearch and friends to get the closest approximation to HMMER bit scores. WARNING: There is a loss of information in this conversion. Neither the scores nor even the rank order of hits will be precisely preserved in a comparison of HMMER hmmsearch to GCG profilesearch. The profile score is an approximation of the (single-hit) HMMER score. Cons %c Gap Len QGap Qlen .. Gap Len .. ! %d %c %5d %5d %5d %5d %5d %5d %5d * fast_algorithms.c%d %d %d %d histogram.cAddToHistogram(): Can't add to a fitted histogram %5s %6s %6s (one = represents %d sequences) obsexp%5s %6s %6s <%4d %6d %6s|oops>%4d %6d %6s|%5d %6d %6d|%5d %6d %6s| %% No statistical fit available %% Statistical details of theoretical EVD fit: mu = %10.4f lambda = %10.4f %% Statistical details of theoretical Gaussian fit: mean = %10.4f sd = %10.4f chi-sq statistic = %10.4f P(chi-square) = %10.4g %-6d %f & hmmio.cr%s.ssiSSIRecommendMode() failedSSIGetFilePosition() failed%s appears to be a binary but format is not recognized It may be from a HMMER version more recent than yours, or may be a different kind of binary altogether. HMMER2.0HMMER v1.9# HMM v1.7# HMM v1.1# HMM v1.0HMMER2.0 [%s] NAME %s ACC %s DESC %s LENG %d AminoNucleicALPH %s yesnoRF %s CS %s MAP %s COM NSEQ %d DATE %s CKSUM %d GA %.1f %.1f TC %.1f %.1f NC %.1f %.1f XT %6s NULT %6s NULE EVD %10f %10f HMM %c d->db->mm->e %6s %6s %6s %6s %6s %6s %6s %6s %6s m->mm->im->di->mi->id->m %6s %6s * %5d %5d %5c // NAME ACC DESC LENG NSEQ ALPH AMINONUCLEICAlphabet mismatch error. I thought we were working with %s, but tried to read a %s HMM. RF CS MAP COM DATE GA TC NC XT NULT NULE ALPH must precede NULE in HMM save filesEVD CKSUMHMM null[converted from an old Plan9 HMM]1.1 ASCII HMMs unsupported1.0 ASCII HMMs unsupported%6d%s%s A nonbiological alphabet size of %d; so I can't convert plan9 to plan7malloc failed for reading hmm in ###MATCH_STATE###INSERT_STATE###DELETE_STATEInvalid argument alpha < 0.0 to SampleGamma()masks.c%s %s %s (%s) HMMEROct 2003Copyright (C) 1992-2003 HHMI/Washington University School of MedicineFreely distributed under the GNU General Public License (GPL)- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Parse failed: expected string, got nothingParse failed: expected integer, got %sParse failed: expected real value, got %sAlignment must have RF annotation to hand-build an HMMmodelmakers.cNo conserved consensus columns found; aborting construction! This is an unusual situation. Reexamine your sequence alignment. It is probably unusually full of gaps, or lots of sequence fragments. You may be able to force HMMER to model it; see the --fast (and --gapmax), or --hand options to hmmbuild.X-PRMX-PRIX-PRT%3d %c %c %c plan7.c Average score: %10.2f bits Minimum score: %10.2f bits Maximum score: %10.2f bits Std. deviation: %10.2f bits plan9.cunnamedNo support for non-protein, non-nucleic acid alphabets.postprob.cprior.cCan't set prior; alphabet type not set yetFailed to open HMMER prior file %s DIRICHLETNo such prior strategy %s; failed to parse file %sHMM and/or sequences are DNA/RNA; can't use protein prior %sHMM and/or sequences are protein; can't use DNA/RNA prior %sAlphabet "%s" in prior file %s isn't valid.%d is bad; need at least one state transition mixture component%d is bad, too many transition components (MAXDCHLET = %d) %d is bad; need at least one match emission mixture component%d is bad; too many match components (MAXDCHLET = %d) %d is bad; need at least one insert emission mixture component%d is bad; too many insert components (MAXDCHLET = %d) PAM prior is only valid for protein sequencesPAM prior may only be applied over an existing Dirichlet priorPAM prior requires that the insert emissions be a single DirichletaaBLASTMATFailed to open PAM scoring matrix file %sFailed to parse PAM scoring matrix file %sFailed to open null model file %s Alphabet type conflict; null model in %s is inappropriate %s is not in HMMER null model file formatX-PRT annotation out of rangeX-PRM annotation out of rangeX-PRI annotation out of rangeHMMER_NCPUtophits.ctophits_s report: Total hits: %d Satisfying E cutoff: %d Total memory: %dK trace.cillegal state transition %s->%s in tracebackillegal state %s in tracebackyo! you don't support J in Traces2Alignment(), remember?Traces2Alignment reports unrecognized statetype %cHMMER %sillegal %s->%s transitionbogus statetype %16s %s CSRF %10.10s %5d %s %-5d %10.10s %5s %s %-5s sanity check failed: didn't find a match state in tracenever happens. Trust me. FATAL: WARNING: PANIC [%s line %d] Unusual errorABCDEFGHIKLMNPQRSTVWXYZ*ACGTUNEFIPQZsqio.c[STDIN]%s: file does not existfilename > 255 char in SeqfileOpen()gzip -dc %sCan't autodetect sequence file format from a stdin or gzip pipeCan't determine format of sequence file %sFailed to read any alignment data from file %sSeqfilePosition() failed: in a nonrewindable data file or streamSSISetFilePosition failed, but that shouldn't happen.SeqfileRewind() failed: in a nonrewindable data file or streamInvalid flag %d to SetSeqinfoString()ACGTUNRYMKSWHBVDacgtunrymkswhbvd///ENTRY TITLEACCESSIONSEQUENCE; DNA sequence, LOCUSDEFINITIONVERSIONORIGINLOCUS >>>>([^ ]+) .+2BIT +Len: ([0-9]+)>>>>([^ ]+) .+ASCII +Len: [0-9]+bogus GCGdata format? %smalloc failedfread failedFile %s does not appear to be in FASTA format at line %d. You may want to specify the file format on the command line. Usually this is done with an option --informat . ID AC ; DE SQ Length: ..>>>>Len: !!AA_SEQUENCE!!NA_SEQUENCE# STOCKHOLM 1.CLUSTALmultiple sequence alignment!!AA_MULTIPLE_ALIGNMENT!!NA_MULTIPLE_ALIGNMENT#=AU#=ID#=AC#=DE#=GA#=TC#=NC#=SQ#=SS#=CS#=RFENTRY MSF:Check: Check: LOCUS ORIGIN ID SQ #%Sequence file contains no data>%s %s Tried to write an aligned format with WriteSeq() -- bad, bad.LOCUS %s %d bp .ACCESSION %s DEFINITION %s VERSION %s ORIGIN >>>>%s 9/95 ASCII Len: %d ENTRY %s TITLE %s ACCESSION %s SUMMARY #Length %d #Checksum %d SEQUENCE 5 10 15 20 25 30 ///NAM %s SRC %s %s %d..%d::%d DES %s SEQ +SS SEQ ID %s AC %s DE %s SQ %d BP %s Length: %d (today) Check: %d .. ; ### from DNA Strider ;-) ; DNA sequence %s, %d bases, %d checksum. ; ;%s %s %8d FASTAGENBANKEMBLGCGGCGDATARAWIGSTRIDERIDRAWZUKERPIRSQUIDSTOCKHOLMSELEXMSFA2MPHYLIPEPSGenbankGCG data libraryrawIntelligeneticsMacStriderIdraw PostscriptZukerStockholmClustala2mPhylipBad code passed to MSAFormat2String()--Option "%s" is ambiguous; please be more specific. %sNo such option "%s". %sOption %s requires an argument %sOption %s does not take an argument %sNo such option "%c". %sOption %s requires an integer argument %sOption %s requires a numerical argument %sOption %s requires a single-character argument %sStrparse(): ntok must be <= %dregexp compilation failed.hsregex.cNULL argument to sqd_regcompregexp too bigout of spacetoo many ()unterminated ()unmatched ()internal error: junk on end*+ operand could be emptynested *?+unmatched []internal error: \0|) unexpected?+* follows nothingtrailing \^$.[()|?+*\internal error: strcspn 0invalid [] rangeNULL argument to sqd_regexeccorrupted regexpregexp corruptioncorrupted pointersinternal error: bad call of regrepeatNULL parameter to sqd_regsubdamaged regexpdamaged match stringregexp(3): %s malloc of %ld bytes failed: file %s line %drealloc of %ld bytes failed: file %s line %dsre_string.cKRQHPLAGVYWFXLysAsnThrArgSerIleMetGlnHisProLeuGluAspAlaGlyVal***TyrCysTrpPheXXXsre_math.cIncompleteGamma(): a must be > 0IncompleteGamma(): x must be >= 0IncompleteGamma(): failed to converge using continued fraction approxIncompleteGamma(): failed to converge using series approxfile.c%s%c%s%s.%s:rbtmp.ssi.1tmp.ssi.2%s %d %lu %lu %lu %s %d %llu %llu %lu %s %s wbenv LC_ALL=POSIX sort -o %s %s ok (no error)no data, fread() failedno such keyout of memory, malloc() failedfile not found, fopen() failednot a SSI file? (bad magic)corrupt format? unexpected datano large file support for this systemfailed to reposition on diskfailed to get file position on diskno fast subseq support for this seqfilesubseq start is out of rangean argument is out of rangenumber of files exceeds limitnumber of keys exceeds limitan fwrite() failedsome problem with external sortingunrecognized code w%s %u %lu %lu %lu %s %u %llu %llu %lu failed to turn external sorting on.0x0Xalignio.c%*s%-10.10s %5d %s %5d %*s %s msa.cfailed to sre_strcat()Parse error: no sequences were found for alignment %sParse error: No sequence for %s in alignment %sParse error: some weights are set, but %s doesn't have one in alignment %sParse error: sequence %s: length %d, expected %d in alignment %sParse error: #=GR SS annotation for %s: length %d, expected %d in alignment %sParse error: #=GR SA annotation for %s: length %d, expected %d in alignment %sParse error: #=GC SS_cons annotation: length %d, expected %d in alignment %sParse error: #=GC SA_cons annotation: length %d, expected %d in alignment %sParse error: #=GC RF annotation: length %d, expected %d in alignment %sfilename > 255 char in MSAFileOpen()Can't autodetect alignment file format from a stdin or gzip pipeCan't determine format of multiple alignment file %sMSAFILE corrupted: bad format indexcan't write. no such alignment format %d File %s does not appear to be an alignment file; rather, it appears to be an unaligned file in %s format. I'm expecting an alignment file in this context. BLOSUM Clustered Scoring Matrixsubstitution matrix,calloc failedFailed to parse PAM matrix scale factor. Defaulting to ln(2)/2!gki.cTotal keys: %d Hash table size: %d Average occupancy: %.1f Unoccupied slots: %d Most in one slot: %d Least in one slot: %d bad primelevel in gki_alloc()Blank name in A2M file %s (line %d) .*:Parse failed at line %d, file %s: possibly using spaces as gapsCLUSTAL W(1.5) multiple sequence alignment %*s %s ^.+MSF: +([0-9]+) +Type: +([PNX]).+Check: +([0-9]+) +\.\.Name: Weight:No Weight: on line %d for %s in name section of MSF file %s Invalid line (probably %d) in name section of MSF file %s: %s Didn't find a sequence for %s in MSF file %s msf.c!!NA_MULTIPLE_ALIGNMENT 1.0 !!AA_MULTIPLE_ALIGNMENT 1.0 WriteMSF(): couldn't guess whether that alignment is RNA or protein. Invalid sequence type %d in WriteMSF() %B %d, %Y %H:%MWhat time is it on earth? strftime() failed in WriteMSF(). squid.msf %s MSF: %d Type: %c %s Check: %d .. Name: %-*.*s Len: %5d Check: %4d Weight: %.2f %*s %-6d%*s%6d %*s %-6d %-*s Failed to parse nseq/alen from first line of PHYLIP file %s nseq and/or alen not an integer in first line of PHYLIP file %s Failed to parse sequence at line %d of PHYLIP file %s %d %d %-10.10s%s Can't read a SELEX format alignment from a pipe, stdin, or gzip'ed fileselex.c#=SAParse error in ReadSELEX()Parse error in #=GA line in ReadSELEX()Parse error in #=TC line in ReadSELEX()Parse error in #=NC line in ReadSELEX()Parse error in #=SQ line in ReadSELEX()Parse error in #=SQ line in ReadSELEX(): weight is not a numberParse error in #=SQ line in ReadSELEX(): incomplete line.:: Parse error in #=CS line in ReadSELEX()Parse error in #=RF line in ReadSELEX()Parse error in #=SS line in ReadSELEX()Parse error in #=SA line in ReadSELEX()#=Parse error in alignment line in ReadSELEX()sequences may be in different orders in blocks of %s?# %s #=ID %s #=AC %s #=DE %s #=AU %s #=GA %.1f %.1f #=GA %.1f #=NC %.1f %.1f #=NC %.1f #=TC %.1f %.1f #=TC %.1f #=SQ %-*.*s %6.4f %s %s %d..%d::%d %s %-*.*s %s TAB characters will corrupt a SELEX alignment! Please remove them first.File %s doesn't appear to be in Stockholm format. Assuming there isn't some other problem with your file (it is an alignment file, right?), please either: a) use the Babelfish format autotranslator option (-B, usually); b) specify the file's format with the --informat option; or a) reformat the alignment to Stockholm format. #=GF#=GS#=GC#=GRStockholm format parse error: line %d of file %s while reading alignment %sDidn't find // at end of alignment %sstockholm.c# STOCKHOLM 1.0 #=GF ID %s #=GF AC %s #=GF DE %s #=GF AU %s #=GF GA %.1f %.1f #=GF GA %.1f #=GF NC %.1f %.1f #=GF NC %.1f #=GF TC %.1f %.1f #=GF TC %.1f #=GF %-5s %s #=GS %-*.*s WT %.2f #=GS %-*.*s AC %s #=GS %*.*s DE %s #=GS %*.*s %5s %s %-*.*s %s #=GR %-*.*s SS %s #=GR %-*.*s SA %s #=GR %-*.*s %5s %s #=GC %-*.*s %s SS_consSA_consIDDEAUGANCTCWTSSSA>*>?<?fff?7'Ŭ>L:o?EJ?Iy?K=<<]/>҉>K^?fs? D*@DD"CDaCD+D!CπD DgCCGC0@@@H@>@@?@j@Ǹ}?@È?⟔]s@!n@#33333>z򚼯H<?@Y?Q?Gdl/cR?.BD@I@Ǹզ?@?zG{?.D5?ə??|hs?PbM@@Ç@$@P@@A.~?gHl@&G<T! hmmpfam - search one or more sequences against HMM databaseUsage: hmmpfam [-options] Available options are: -h : help; print brief help on version and usage -n : nucleic acid models/sequence (default protein) -A : sets alignment output limit to best domain alignments -E : sets E value cutoff (globE) to ; default 10 -T : sets T bit threshold (globT) to ; no threshold by default -Z : sets Z (# models) for E-value calculation --acc : use HMM accession numbers instead of names in output --compat : make best effort to use last version's output style --cpu : run threads in parallel (if threaded) --cut_ga : use Pfam GA gathering threshold cutoffs --cut_nc : use Pfam NC noise threshold cutoffs --cut_tc : use Pfam TC trusted threshold cutoffs --domE : sets domain Eval cutoff (2nd threshold) to --domT : sets domain T bit thresh (2nd threshold) to --forward : use the full Forward() algorithm instead of Viterbi --informat : sequence file is in format --null2 : turn OFF the post hoc second null model --pvm : run on a PVM (Parallel Virtual Machine) cluster --xnu : turn ON XNU filtering of query protein sequence GGGGGGGGHH HH$H0H8H@HLHXH`Hh6;:8/;T:P9L7&0R  >6]}=g=ĥ===*=n3=]>p7 >d=#7<]U>j=\;vH<f<^<(U<@]S<2N>t /?=:'>q?Cs=>>\;>n&?C>}At=>>3?!>Y?Y>#>h<= ="<6=zW?==4=.6 <8bI;};C>i<1?۱>W;;8h4[=BE>7<1N= =K@`=L߭=\!=bV=6=3=8==,>>=͈? >sm?3]>=N=ǞZ>>>>?)hs=| >L(p;* ;Y;D9;Ȓ;cGc<;o;!q;vl;G:;?<[l;mK;׶5;OT;q;Br;5q;0k(kDkL >>>>=;< =Y4=q=&=.w<=j=sKQ=G<=9'=I=$C=S>6==kT=5?L XnV?(F4?=jΪ?gZ_?󭀡{k?J?K5?v1?Цv ?g@;"`B?4=h? @B?d?Wۉ(?ɗ}?NA?2c)?8?[L ?Ĕ{+?x?@g?¬ﷳ`?%?4?5cV?@*z?fn6? %B?cm? !?$Q ?0?ʊ?)/2?rH?I%F9?bfZ?oMש?vF!?|1ޟ](?յ *9\?X$?O`epr?֡af?p؄?Okx?EOP?[t]? cj?s~Q??ә?.?1!?@: ?cQ0P?tiA?Ȑ? 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