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LL I 8ML{LdHD$(8@ǀuH?D<@Q tHD$(HD$(t <,u.LHEH-L=HV6L%M-1H H5H=1胗H HH= HIHD$(E1E1E1HD$A< < t I_IHt$1L H\$(HI9eH=Y;-Ht$L{1L H\$(II9,H= H9;:AuHHt$L{1LHD$6 H\$(II9H@LL$H=vIAL1H)ILxIK'L9rWI?@LFM9vMK?IK46LLL$LD$ LD$HLL$uL< H=\IK$1LL9t f,pLHOd < uH< t<,uHL-L%H=1蝕|$'t-H=HH;@ǀuHD<@tHH5fHw u HEH5JHT t H7!H1@JtH;@ǀuHD<݀;tH=譔H=HH;@ǀuHD<@tHɀ;fH5H tH5Ho uHIH\$(aHt$( H IA8HD$(8@ǀuHT<@1҅…tHD$(HD$(8@t}kt" ʚ;gmtHttv@BHD$(HD$(8@ǀuHuT<@1҅…uHD$(8u%H1HHII9HF˃H t@KH5V1H= גuH#Hu)HHu HdHH9vHH=zH\$(H=jH=HtHt$(H=sLu@H=HuEH|$(wH=%H=1tH=H1ԑH8[]A\A]A^A_RH5H=/tH=13H=ay1HxPXH BPH5 BH=H AP H5AH= H APyH5AH=vH APH5AH=VH AP H5AH='6H iAPH5iAH=H IAPH5IAH=MH )APH5)AH=#H BPzH5 AH=8H !LPH5%@%B%D%F%H%J%L%N%P%R%T%V%X%Z%\%^%`%b%d%f%h%j%l%n%p%r%t%v%x%z%|%~%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % %%%%%%%%%% %"%$%&%(%*%,%.%0%2%4%6%8%:%<%>%@%B%D%F%H%J%L%N%P%R%T%V%X%Z%\%^%`%b%d%f%h%j%l%n%p%r%t%v%x%z%|%~%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%LMAS%=hhhhhhhhhhhhxhnhdhZhPhFhh4h*h hh hhhhhhhhhhhhhhhvhlhbhXhNhDh:h0h&hhhhhhhhhhhhhhhhh|hrhhh^hThJh@h6h,h"hhhhhhhhhhhhhhhhhxhnhdhZhPhFh,-}in,infileiHMM input fileshmm-inspecify HMMs for individual sequenceshmm-batchDealign input sequencesdealignPre-aligned multiple sequence file (aligned columns will be kept fix)profile1,p1profile2,p2disable check if profile, force profile (default no)is-profileForce a sequence type (default: auto){Protein, RNA, DNA}seqtypetForced sequence input file format (default: auto){a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]}infmtin Clustal format print residue numbers (default no)residuenumber,resno Clustering:Pairwise alignment distance measure{ktuple}pairdistpPairwise distance matrix input file (skips distance computation)distmat-inPairwise distance matrix output filedistmat-outGuide tree input file (skips distance computation and guide-tree clustering step)guidetree-inGuide tree output fileguidetree-outSequentially align sequencespileupUse full distance matrix for guide-tree calculation (might be slow; mBed is default)fullUse full distance matrix for guide-tree calculation during iteration (might be slowish; mBed is default)full-itersoft maximum of sequences in sub-clusterscluster-sizeClustering output fileclustering-outuse transitivity (default: 0)transPosterior probability output fileposterior-outuse Kimura distance correction for aligned sequences (default no)use-kimuraconvert distances into percent identities (default no)percent-idClustering method for guide tree{UPGMA}clusteringc Alignment Output:Multiple sequence alignment output file (default: stdout){file,-}out,outfileoMSA output file format (default: fasta)outfmtnumber of residues before line-wrap in outputwrapMSA output order like in input/guide-tree{input-order,tree-order}output-order Iteration:Number of (combined guide-tree/HMM) iterationsiterations,iterMaximum number of guidetree iterationsmax-guidetree-iterationsMaximum number of HMM iterationsmax-hmm-iterations Limits (will exit early, if exceeded):Maximum allowed number of sequencesmaxnumseqMaximum allowed sequence lengthmaxseqlen Miscellaneous:Set options automatically (might overwrite some of your options)autoNumber of processors to usethreadsInput file for pseudo-count parameterspseudoLog all non-essential output to this fileloglPrint this help and exithelphPrint version information and exitversionPrint long version information and exitlong-versionVerbose output (increases if given multiple times)verbosevForce file overwritingforceMAC-RAMinsufficient memory (for argtable allocation)1.2.3Clustal Omega%s - %s (%s) If you like Clustal-Omega please cite: %s If you don't like Clustal-Omega, please let us know why (and cite us anyway).Check http://www.theclustal.com for more information and updates.Usage: %sA typical invocation would be: %s -i my-in-seqs.fa -o my-out-seqs.fa -v See below for a list of all options. %-25s %s clustal-omegaFor more information try: %s --help Use --force to force overwriting.Cowardly refusing to overwrite already existing file%s '%s'. %sSorry, I do not have permission to write to file '%s'.File '%s' does not exist.proteinrnadnaUnknown sequence type '%s'ktupleUnknown pairdist method '%s'upgmaUnknown guide-tree clustering method '%s'Automatic iteration not supported at the moment.Couldn't iteration parameter: %sUnknown output format '%s'Changing number of threads to %d doesn't make sense.input-ordertree-ordersReading sequence file '%s' failedFile '%s' contains %d sequence%s, nothing to alignnot more sequences (%d) than cluster-size (%d), turn off mBedDealigning already aligned input sequences as requested.Reading sequences from profile file '%s' failedSequences in '%s' are not aligned, i.e. this is not a profileAn error occured during the alignmentCould not save alignment to %sSuccessful program exit Sievers F, Wilm A, Dineen D, Gibson TJ, Karplus K, Li W, Lopez R, McWilliam H, Remmert M, Söding J, Thompson JD, Higgins DG. Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol Syst Biol. 2011 Oct 11;7:539. doi: 10.1038/msb.2011.75. PMID: 21988835.Sep 28 2016AndreaGiacomoversion %s; code-name '%s'; build date %sRead distances *and* guide-tree from file doesn't make sense.Won't be able to save distances to file, because I got a guide-tree as input.Got a guide-tree as input and output which doesn't make sense when not iterating.Memory for MAC Algorithm quite low, Viterbi Algorithm may be triggered.Viterbi Algorithm always turned on, increase MAC-RAM to turn on MAC.option: auto-options = %d option: distmat-infile = %s option: distmat-outfile = %s option: clustering-type = %d option: pair-dist-type = %d option: use-mbed = %d option: use-mbed-for-iteration = %d option: pile-up = %d option: guidetree-outfile = %s option: guidetree-infile = %s option: hmm-input no %d = %s option: hmm-input-files = %d option: num-iterations = %d option: iterations-auto = %d option: max-hmm-iterations = %d option: max-guidetree-iterations = %d option: iMacRamMB = %d option: percent-id = %d option: use-kimura = %d option: clustering-out = %s option: posterior-out = %s Couldn't exec %sHMMER Sequences need to be aligned to create an HMM/tmp/clustalo_tmpaln_XXXXXXCould not create temporary alignment filenameCould not convert alignment %s into HHMRemoving %s failed. Continuing anywayCould not find suitable HMMER binarieshmmbuild %s %s >/dev/null && hmmcalibrate %s >/dev/nullCommand '%s' failed/tmp/clustalo_tmphmm2_XXXXXXCould not create temporary hmm filenamehmmbuild %s %s >/dev/null && hmmconvert -2 %s > %sUsing HMMER version %d to calculate a new HMM./tmp/clustalo-hmm-iter_XXXXXXAlnToHMMFile() on %s failed.Processing of HMM file %s failedUsing %d threadsFIXME: Untested...Set up first leaf with node counter %d: left=%d right=%d parent=%dSet up merge node with node counter %d: left=%d right=%d parent=%dSet up leaf with node counter %d: left=%d right=%d parent=%dHave only two sequences: No need to compute pairwise score and compute a tree.Have only two sequences: Will not calculate/print distance matrix.Reading guide-tree from %sReading of guide tree %s failed.Can't input distance matrix when in mbed mode.mbed execution failed.Guide-tree computation (mBed) done.Ignoring request to write distance matrix (am in mBed mode)Couldn't compute pair distancesGuide-tree computation done.clustering method should have been checked beforeINTERNAL ERROR %sNot using weightsleft/right order after tree traversal%3d: %2d/%2d -> %d Setting options automatically based on input sequence characteristics (might overwrite some of your options).Auto settings: Enabling mBed.Auto settings: Disabling iterations.Auto settings: Setting iteration to 1.Background HMM %s for %s (%d/%d) does not existprint frequencies....%3d: %1.3fInput sequences are aligned. Will turn alignment into HMM and add it to the user provided background HMMs.Couldn't convert aligned input sequences to HMM. Will try to continueTurning profile1 into HMM and will use it during progressive alignment.Couldn't convert profile1 to HMM. Will try to continueWill use Kimura distances of aligned sequences.Input sequences are aligned.AlignmentOrder() failed. Cannot continueiMaxHMMIterations < 0 (%d), will not perform alignmentAlignment score for first alignment = %fReached maximum number of HMM and guide-tree iterationsIteration step %d out of %dIteration step %d out of Computing new guide tree (iteration step %d)Skipping guide-tree iteration at iteration step %d (reached maximum)Computing HMM from alignmentCouldn't convert alignment to HMM. Will stop iterating now...Skipping HMM iteration at iteration step %d (reached maximum)Alignment score for alignmnent in hmm-iteration no %d = %f (last score = %f)Performing profile/profile alignmentAlignment score is = %fCouldn't convert alignment to HMM. Will not do posterior probabilities...File %s with pseudo-count parameters does not exist no token specifying pseudo-count parameter in file %s no line with parameter in file %s associated with %s no token in 2nd line in file %s associated with %s token in file %s associated with %s not valid double (%s) gapbgapdgapegapfgapggaphgapipcapcbpccgapbVgapdVgapeVgapfVgapgVgaphVgapiVpcaVpcbVpccV%s not a valid pseudo-count parameter must be one of [gapb,gapd,gape,gapf,gapg,gaph,gapi,pca,pcb,pcc,gapbV,gapdV,gapeV,gapfV,gapgV,gaphV,gapiV,pcaV,pcbV,pccV] ACDEFGHIKLMNPQRSTVWYACGUin seq %d re-translated %d residue codes (%d true, %d case)inconsistency in un/aligned sequence %d >%s >%s #1.i 2.name 3.L1 4.L2 5.sum 6.sum/L1 7.HH Viterbi%d %10s %3d %3d %f %f %fViterbi algorithm triggered %d times (out of %d)Progressive alignment progressCouldn't convert alignment to HMM. Will not proceed with chained alignment, step %dFIXME: Using only first of %u HMMs (needs implementation)Dealigning aligned sequences (inside %s)merge profiles at node %dmerging profiles %d & %dL/#=%3d (ID=%3d, w=%f): %s R/#=%3d (ID=%3d, w=%f): %s hhalign_wrapper.c%s:%s:%d: (not essential) HMM pre-alignment failed, error %d, #=%d (len=%d), lead-seq=%s, len(HMM)=%d %s CARRY ON REGARDLESS strlen(prof1)=%d, strlen(prof2)=%d -- nothing to align %s:%s:%d: problem in alignment (profile sizes: %d + %d) (%s + %s), forcing Viterbi hh-error-code=%d (mac-ram=%d) %s%s:%s:%d: problem in alignment, Viterbi did not work hh-error-code=%d (mac-ram=%d) %scould not perform alignment -- bailing out %s:%s:%d: 2nd attempt worked@@iL=%d, #(iL)=%d, iR=%d, #(iR)=%d @@>%s @@node %3d, #leaves=%d: Alignment scores with HMM:%2d: %f %d,Unknown character in seq '%s'Internal error in %s: Unknown sequence type.ACGTUN-ABCDEFGHIKLMNPQRSTUVWXYZ-(Partial alignment)K-tuple distance for sequence pair %d:%d = %lgWARNING: ERROR: CRITICAL ERROR: FORCED DEBUG: FATAL: Could not compute pairwise distances for mbed.Using %d seeds (randomly chosen) for mBed (from a total of %d sequences)Using %d seeds (chosen with constant stride from length sorted seqs) for mBed (from a total of %d sequences)Internal error: unknown seed selection typePicked sequence %d (%s) as seed no %dSkipping this split because objs in 1st/2nd cluster = %d/%d < %d%s(): Can't split cluster no. %d which has %d objects any further. %sHope it's not too big and doesn't slow things down.Internal error: split into more than two clusters (got assignment %d)Bisecting K-means finished after %d rounds (no more clusters to split)Computing real distances within subclusters for mBed.Automatically determined number of seeds is bigger (or equal) the number of sequences. Will set it to %dCould not convert sequences into vectors for mbedmBed created %u cluster/s (with a minimum of %d and a soft maximum of %d sequences each)Cluster %u: object %u has index %u (=seq %s %d~len) %s Memory allocation for pre-cluster distance-matrix failedSubcluster-%uDistance calculation within sub-clustersCalling new Mbed use makes only sense if nseq>MAX_ALLOWED_SEQ_PER_PRECLUSTERCouldn't open %s for writingNULL != treemuscle_tree.cuNodeIndex1 < tree->m_uNodeCount && uNodeIndex2 < tree->m_uNodeCounttree->m_uNeighbor3[uNodeIndex1] == uNodeIndex2tree->m_uNeighbor3[uNodeIndex2] == uNodeIndex1IsEdge(uNodeIndex1, uNodeIndex2, tree)%sungetc failedfgetc reached end of fileTree::GetToken: input buffer too small, token so far='%s'():;,End-of-file skipping white spacetree!=NULLuNodeIndex1 < tree->m_uNodeCountuNodeIndex2 < tree->m_uNodeCounttree->m_bRooted && uNodeIndex < tree->m_uNodeCountuNodeIndex < tree->m_uNodeCountNULL != tree->m_uNeighbor1NULL != tree->m_uNeighbor2NULL != tree->m_uNeighbor3IsLeaf(uNodeIndex, tree)IsRooted(tree)Missing edge length in tree %u-%u, :%g( ; FIXME: output of unrooted muscle trees not implementedAssertAreNeighbors(%u,%u), are %u nodesAssertAreNeighbors(%u,%u) failedHasEdgeLength(%u, %u)=%c HasEdgeLength(%u, %u)=%c Tree::AssertAreNeighbors, HasEdgeLength not symmetricTree::AssertAreNeighbors, Edge length disagrees %u-%u=%.3g, %u-%u=%.3gTree::ValidateNode: Node %u has two neighbors, tree is not rootedTree::ValidateNode: Node %u has two neighbors, but not root node=%uTree::ValidateNode, n2=null, n3!=nullTree::ValidateNode, n3=null, n2!=nullTree::ValidateNode, duplicate neighbors in node %uTree::ValiateNode(%u), no parentTree::ValidateNode(%u), parent / child mismatchtree has not been created%s(): %sNULL_NEIGHBOR == tree->m_uNeighbor2[uExistingLeafIndex]NULL_NEIGHBOR == tree->m_uNeighbor3[uExistingLeafIndex]uExistingLeafIndex < tree->m_uNodeCountAppendBranch(%u): not leafTree::GetGroupFromFile, expected ',', got '%s'Tree::GetGroupFromFile, expected ')' or ',', got '%s'Tree::GetGroupFromFile, expected '(' or leaf name, got '%s'Tree::GetGroupFromFile, expected edge length, got '%s'ftree!=NULLCouldn't open tree-file '%s' for reading. Skipping *** Warning *** edge length on root group in Newick file %s Tree::FromFile, expected ';' or ',', got '%s'Tree::Unroot, not rootedNULL_NEIGHBOR == tree->m_uNeighbor1[0]IsRoot(0, tree)This is a tree with %u nodes, which is rooted: Index Parnt LengthP Left LengthL Right LengthR Id Name ----- ----- ------- ---- ------- ----- ------- ----- ---- unrooted; Index Nbr_1 Length1 Nbr_2 Length2 Nbr_3 Length3 Id Name ----- ----- ------- ----- ------- ----- ------- ----- ---- %5u %7.3g * *%5u [ROOT] %suNodeIndex < prTree->m_uNodeCountInternal error in %s: sub=%uNULL!=treeInternal error: node index out of rangeNULL!=prDstTreeNULL!=prSrcTreeuDstTreeReplaceNodeIndex < prDstTree->m_uNodeCountIsLeaf(uDstTreeReplaceNodeIndex, prDstTree)IsRooted(prDstTree) && IsRooted(prSrcTree)v < (g_uLeafCount*(g_uLeafCount - 1))/2muscle_upgma.cTriangleSubscript(%u,%u) %udistmat->nrows==distmat->ncolsuInsane != RminuInsane != g_uNodeIndex[Rmin]Lmin != uInsaneRmin != uInsanedtMinDist != BIG_DISTUPGMA2: Invalid LINKAGE_%ug_uInternalNodeIndex < g_uLeafCount - 1 || BIG_DIST != dtNewMinDistg_uInternalNodeIndex < g_uLeafCount - 1 || uInsane != uNewNearestNeighborSequences need to be aligned (%s)Pairwise distance calculation progressAligned distance for sequence pair %d:%d= %lgUsing Kimura distance corretion which includes Dayhoff substitution table lookup for non-protein sequencespair_dist.cInternal error in %s:%sPlease use distance matrix input only, if you know exactly what you're doing!Reading distance matrix failedCalculating pairwise ktuple-distances...Ktuple-distance calculation progressCalculating pairwise aligned identity distances...Pairwise identity calculation progressCalculating Kimura-corrected pairwise aligned identity distances...INTERNAL ERROR: don't know about pairdist_type %dPairwise distance matrix written to %s%s: %lu %%%s (%lu out of %lu)%s done. CPU time: Cannot report all and sample at the same time. Skipping %s()Sequences are not aligned. Skipping %s()LOW ID(TO)HIGH IDLEN %-15s %5s %7s %-15s %7s %-15s --------------- ----- ------- --------------- ------- ---------------* %-15s %5d %7.1f %-15s %7.1f %-15s Alignment name: %s Number of sequences: %d Total # residues: %d Smallest: %d Largest: %d Average length: %.1f Alignment length: %d Average identity: %.2f%% Most related pair: %.2f%% Most unrelated pair: %.2f%% Most distant seq: %.2f%% sqinfo->name = %ssqinfo->id = %ssqinfo->acc = %ssqinfo->desc = %ssqinfo->len = %dsqinfo->start = %dsqinfo->stop = %dsqinfo->olen = %dsqinfo->type = %dsqinfo->ss = %ssqinfo->sa = %sDNARNAProteinUNKNOWNWill never get hereInternal error in %sUnknown output format chosenwCould not open file %s for writinginvalid output format should have been detected beforeinternal error: %sAlignment written to %sFIXME: This modifies sequence ordering. Might not be what user wants. Will change output order as wellPotential Problem: sequences (N=%d) don't have same lengths but contain gaps, consider using --dealign-Failed to open sequence file %s for readingMaximum number of sequences (=%d) exceeded after reading sequence '%s' from '%s'Sequence '%s' has %d residues and is therefore longer than allowed (max. sequence length is %d)Sequence '%s' has 0 residuesOverriding automatically determined seq-type %s to %s as requestedCouldn't guess sequence type from first sequenceseq-no %d: type=%s name=%s len=%d seq=%sACGTRead %d sequences (type: %s) from %sFailed to open HMM-batch file %s for readingsequence %s not found in input sequences (%s), will be ignoredWas asked to add 0 sequencesJoining sequences of different typesymmatrix.cCouldn't allocate memory (%s|%s) Couldn't allocate MPI memory (%s|%s) One of the provided arguments is empty or NULL (print_matrix) Couldn't open %s for writing.%u %u x %u %-*s %fERROR: couldn't allocate memory at %s:%s:%d ERROR: Couldn't open %s for reading Couldn't read first line from %s Looks like I couldn't read complete line. Wrong format (or too small MAX_BUF_SIZE)%dERROR: couldn't parse number of sequences from first line of %s Memory allocation for distance matrix failedFATAL %sSequence ordering in mseq and distmat differ (expected %s and got %s from distmat %s)n%lfCouldn't parse float from entry '%s' expected %d seqs, but only parsed %d Couldn't open tree-file '%s' for writing. Skippingtree logging...Guide tree written to %sMuscleTreeFromFile failedUser tree must be rootedUser tree does not match input sequencesLabel '%s' in tree could not be found in sequence namesSequence index out of range during tree traversal (leafid=%d nseqs=%d)Tree traversal: Visited leaf-node %d (leaf-id %d = Seq '%s')Tree traversal: Visited non-leaf node %d with siblings %d (L) and %d (R)rOut of memory (requested from %s:%d) FATAL: Out of memory (requested from %s:%d) Bad call to CkFree from %s:%d (pointer was NULL) Internal error: unknown order %cCouldn't close temporily created file %s. Expect trouble...Removing of temporarily created file %s failed. Expect trouble...Error: Di=%i: n[%i][X[%i]]=0! (X[%i]=%i) Function substr: >1000 chars to copy. Exiting.Command: ! ERROR when executing: Error in hhutil-C.h: wrong format while reading file '. : could not open file '' : Memory overflow while creating ''. Please report this bug to developers : . Please report this bug to developers HOMEWarning: could not find ./.hhdefaults or Arguments read in from .hhdefaults:Warning: no default options for '' found in Argument: %s Using the BLOSUM%2i matrix Using the Gonnet matrix : sequence identity = %2.0f%%; entropy per column = %4.2f bits (out of %4.2f); mutual information = %4.2f bits Check matrix: before renormalization sum P(a,b)= ... A R N D C Q E G H I L K M F P S T W Y V p[] %4.1f Substitution matrix log2( P(a,b)/p(a)/p(b) ) (in bits): Odds matrix P(a,b)/p(a)/p(b): Matrix of conditional probabilities P(a|b) = P(a,b)/p(b) (in %): Probability matrix P(a,b) (in %): A R N D C Q E G H I L K M F P S T W Y V %5.0f Similarity matrix P(a,b)^2/P(a,a,)/P(b,b) (in %): %4.0f A C G T U ? ? ? ? ? ? ? ? ? ? ? ? ? ? ? WARNING: could not read line '' in HMM in array of names for sequences to displayNAMEReading in HMM : FAMFILELENGFILTNSEQNEFFNAA%fEVD%f %fDESCCOMDATESEQRead from file:>ss_dssp>sa_dssp>ss_pred>ss_conf>Cons->Consensusarray of sequences to displayWARNING: Ignoring following line while reading HMM: 'nss_dssp=%i nsa_dssp=%i nss_pred=%i nss_conf=%i nfirst=%i >(k=) FREQError: hhm file has obsolete format. Please use hhmake version > 1.1 to generate hhm files. AVERNULL NULL %5.1f HMMWARNING: in HMM state is followed by state WARNING: further warnings while reading HMMs will be suppressed. there are more columns than the stated length . Skipping HMM %s%6i %5i %5.1f %5.1f %5.1f WARNING: Ignoring line 'HMM %s is already calibrated: lamda=%-5.3f, mu=%-5.2f Warning: in HMM there are only columns while the stated length is WARNING: maximum number of residues exceeded while reading HMM WARNING: HMM contains no match states. Check the alignment that gave rise to this HMM. Read in HMM with match states and effective number of sequences = HHWARNING: invalid symbol '' at pos. in line '' of HMM ACC ALPHAminoNucleichhhmm-C.h%s:%s:%d: WARNING: HMM reading does not work for DNA/RNA RF CS MAP COM CKSUM GA TC NC SADSS WARNING: HMM %s has SADSS records with more than %i residues. SSPRD WARNING: HMM %s has SSPRD records with more than %i residues. SSCONSSCITXT NULTNULEEVD Warning: some HMMs have been calibrated with HMMER's 'hmmcalibrate'. These calibrations will be ignored Error: in HMM HMMERaminoSTATS LOCALEFFNCOMPO NULL %6.3g Error: Adding transition pseudocounts to linear representation of %s not allowed. Please report this error to the HHsearch developers. Error: Adding transition pseudocounts twice is %s not allowed. Please report this error to the HHsearch developers. Pseudocount transition probabilities:pM2M=%4.1f%%, pM2I=%4.1f%%, pM2D=%4.1f%%, pI2M=%4.1f%%, pI2I=%4.1f%%, pD2M=%4.1f%%, pD2D=%4.1f%% tau = %4.1f%% Listing transition probabilities WITH pseudocounts: i dssp pred sacc M->M M->I M->D I->M I->I D->M D->Dnss_dssp=%i nss_pred=%i %4i %1c %1c %1c %6.3f %6.3f %6.3f %6.3f %6.3f %1i %2i %1i Col SS II%3i %c %2i Average amino acid frequencies A R N D C Q E G H I L K M F P S T W Y V Q: T: Null: pb: Error: Writing transition pseudocounts in linear representation not allowed. Please report this error to the HHsearch developers. stdoutaWriting HMM to HHsearch 1.5 NAME %s FAM %s FILE %s COM DATE %sLENG %i match states, %i columns in multiple alignment FILT %i out of %i sequences passed filter (-id %i -cov %i -qid %i -qsc %.2f -diff %i) NEFF %-4.1f %s <%i characters> # NULL >%s %-.*s * %i HMM %1c M->M M->I M->D I->M I->I D->M D->D Neff Neff_I Neff_D %-i %1c %-4i Recording calibration coefficients in Error: wrong format in %s. Expecting hhm format space to read in HHM file for calibrationEVD %-7.4f %-7.4fWARNING in : no calibration coefficients written to Could not open file for writing. HMMER2.0 [hhmake %s] DESC %s LENG %i ALPH Amino RF yes CS yes MAP yes NSEQ %i SSDSS %s SADSS %s SSPRD %s SSCNF %s XT %6i %6i %6i %6i %6i %6i %6i %6i NULT -4 -8455 NULE * %6i %1c m->m m->i m->d i->m i->i d->m d->d b->m m->e %6i * %6i %5i %1c * * * * * * * * * * * * * * * * * * * * %1c 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 %1c %6i * * * 0 * * HHHHHNeutralized His-tag at position %i start:%i end:%i EQKLISEEDLDYKDDDDKNeutralized C-myc-tag at position %i Neutralized FLAG-tag at position %i Divergence before / after addition of amino acid pseudocounts: %5.2f / %5.2f No pseudocounts added (-pcm 0) Adding constant AA pseudocount admixture of to HMM Adding divergence-dependent AA pseudocounts (-pcm 2) with admixture of Average amino acid frequencies WITH pseudocounts in HMM: Prof: Amino acid frequencies WITHOUT pseudocounts: A R N D C Q E G H I L K M F P S T W Y V Amino acid frequencies WITH pseudocounts: A R N D C Q E G H I L K M F P S T W Y V %3i: sum=%5.3f of sequences exceded in file Error: sequence contains no residues.array for input sequences>ss_>sa_>aa__consensusReading seq %-16.16s k=%3i n_displ=%3i display[k]=%i keep[k]=%i array for sequence namesWARNING: No sequence name preceding following line in in line of WARNING: maximum number of residues exceded in sequence Error: no sequences found in file Read sequences Query sequence for alignment has number (0 is first) Using match state assignment by capital letters (a2m format) Using percentage-rule match state assignment Using residues of first sequence as match states abcdefghiklmnpqrstuvwxyz.WARNING: input alignment %s looks like aligned FASTA instead of A2M/A3M format. Consider using '-M first' or '-M 50' Error: Alignment in contains no match states. Consider using -M first or -M optionWARNING: Number of match columns too large. Only first %i match columns will be kept! Alignment in contains match states percent gaps[]= first seq: columns and Length of first seq = %i . Check input format for '-M a2m' option and consider using '-M first' or '-M 50' NOTE: Use the '-cons' option to calculate a consensus sequence as first sequence of the alignment.Error: sequences in do not all have the same number of columns, e.g. first sequence and sequence . %i out of %i sequences passed filter (%i%% min coverage, %i%% min sequence identity to query, %.2f bits min score per column to query, up to %i%% position-dependent max pairwise sequence identity) %i%% max pairwise sequence identity) k=%3i score=%6.2f Error: Ii=%i: n[%i][X[%i]]=0! (X[%i]=%i) Calculating position-dependent weights on subalignments Matches:col Neff nseqs%3i %5.2f %3i Inserts: Deletes:array of names for displayed sequencesEffective number of sequences exp(entropy) = %-4.1f Matr: Amino acid frequencies without pseudocounts: A R N D C Q E G H I L K M F P S T W Y V Listing transition probabilities without pseudocounts: i M->M M->I M->D I->M I->I D->M D->D Neff_M Neff_I Neff_D%3i: %4i %6.3f %6.3f %6.3f %6.3f %6.3f %6.3f %i out of %i core alignment sequences passed filter ( out of sequences filtered by minimum score-per-column threshold of Writing alignment to #%s a3mWriting A3M alignment to >%s %s Writing PSI-BLAST-formatted alignment to %-20.20s hhalignment-C.h****************%s:%s:%d: did get into MergeMasterSlave Merging %s to query alignment WARNING in %s: maximum number of %i sequences exceeded while reading %s. Skipping all following sequences Error: did not find %i match states in sequence %i of %s. Sequence: %s L is not set in AddSequence()%s:%d: Arena[%d]=NULL, cnt=%d %s:%s:%d: profile has no leading and/or trailing residues (h=%d:t=%d:#=%d) Error: out of memory while allocating row %i (out of %i) for dynamic programming matrices Suggestions: 1. Cut query sequence into shorter segments 2. Check stack size limit (Linux: ulimit -a) 3. Run on a computer with bigger memory Bwd scale %3i Post scale %3i: %9.3G %7.4f Forward total probability ratio: %8.3G hhhit-C.h%s:%s:%d: B_MM[1][1]=%g, B_IM[1][1]=%g, B_MI[1][1]=%g, B_DG[1][1]=%g, B_GD[1][1]=%g %s:%s:%d: Backward score is %g %s:%s:%d: B_MM[%d][%d]=%g, B_MM[%d][%d]=%g, B_MM[%d][%d]=%g Score %3i Template=%-12.12s i=%-4i j=%-4i score=%6.3f %2i: %5.2f Fwd scale %s:%s:%d: length(s) of profile(s) invalid (q.L=%d/t.L=%d) %s:%s:%d: F_MM[i][j]=%g, F_IM[i][j]=%g, F_MI[i][j]=%g, F_DG[i][j]=%g, F_GD[i][j]=%g (i=%d,j=%d) %s:%s:%d: Forward score is %g, Pforward is %g space for alignments with database HMMs. Note that all alignments have to be kept in memoryspace for alignments with database HMMs. Note that all sequences for display have to be kept in memoryspace for HMM-HMM alignmentsError: unallowed state value %i occurred during backtracing at step %i, (i,j)=(%i,%i) NAME=%7.7s score=%7.3f score_ss=%7.3f step Q T i j state score T Q cf ss-score%4i %1c %1c %4i - %1c %4i %1c - %4i %4i %2i %7.2f %c %c %1i %7.2f step Q T i j state score T Q cf ss-score P_post Sum_post%4i %4i %2i %7.1f %c %c %1i %7.1f %7.5f %7.2f space for formatting HMM-HMM alignmentWarning: sequence in HMM has match states but should have i chr m l%3i %1c %3i %3i %d: j1=%d -> temp has leading gaps %d: i1=%d -> query has leading gaps +-------------------------------+ | both sequences truncated left | +-------------------------------+ i1 = %d, j1 = %d %d: j2=%d (%d) -> temp has trailing gaps %d: i2=%d (%d)-> query has trailing gaps +--------------------------------+ | both sequences truncated right | +--------------------------------+ i2 = %d != %d = qa->L, j2 = %d != %d = ta->L Probab=%-.2f E-value=%-.2g Score=%-.2f Aligned_cols=%i Identities=%i%% Similarity=%-.3f Sum_probs=%.1f Q %-*.*s %1cQ %-*.*s %4i %4i (%i) %*.*s T %-*.*s %4i T %-*.*s Query %s Match_columns %i No_of_seqs %i out of %i Neff %-4.1f Searched_HMMs %i Date %sCommand No Hit Prob E-trans E-value Score SS Cols Query HMM Template HMM No Hit Prob E-value P-value Score SS Cols Query HMM Template HMM %3i %-30.30s %-34.34s %5.1f %7.2G %7.2G %6.1f %5.1f %4i %4i-%-4i %-10.10s%4i-%-4i%-9.9s(%i) hhhitlist-C.h%s:%s:%d: qt_ali.Build failed WARNING: maximum likelihood fit of score distribution did not converge. %3i %-7.3f %-7.3f %-12.8f %-9.3E k=%4i %4i:%6.3f Householder reduction to bidiagonal formi=%i Accumulation of right-hand transformations Accumulation of left-hand transformations Diagonalization of the bidiagonal formk=%i Error in SVD: no convergence in 30 iterationsError: InvertMatrix called with matrix of dimension 0%i hhfunc-C.h%s:%s:%d: WARNING -- Background Pseudocounts point to NULL this is not intended - don't add background but CONTINUE alignment%s:%s:%d: expected to re %s from file but no file specified %s:%s:%d: expected to read HMM from file but no file-name HMMER3Query file is in HMMER3 format WARNING! Use of HMMER3 format as input results in dramatically loss of sensitivity! Query file is in HMMER format WARNING! Use of HMMER format as input results in dramatically loss of sensitivity! WARNING: HMM %s looks too diverse (Neff=%.1f>11). Better check the underlying alignment... Query file is in HHM format %s:%s:%d: Unknown HMM format in infile infile=%s, #seq=%d %s:%s:%d: was expecting internal alignment but ppcProf=%p, #seq=%d, ppcProf[0][0]=%c %s:%s:%d: was expecting to read alignment from file but no filename Error in %s: only HHM files can be calibrated. Build an HHM file from your alignment with 'hhmake -i %s' and rerun hhsearch with the hhm file stdin is in A2M, A3M or FASTA format WARNING: alignment %s looks too diverse (Neff=%.1f>11). Better check it with an alignment viewer... %s:%s:%d: was expecting to copy HMM structure but L=%d %s:%s:%d: RE-CYCLING HMM Warning from hash.C: key=NULLTransitive score Ztq: mu=%8.3g sigma=%8.3g rbNo 'Database:' string found.No integer for number of sequences in database found.No integer for size of database found. Number of sequences in database = %i Size of database = %i Expect =No 'Expect =' string found.%gNo Evalue found after 'Expect ='.template=%-10.10s length=%-3i EvalDB=%8.2g EvalQT=%8.2g P-value=%8.2g log Pval=%8.2g sequences;Length =WARNING: idummy should have been ==2 (no length correction)Calculate Pvalues as a function of query and template lengths and diversities...WARNING: global calibration not yet implemented!!!!!!!!!!!!!!!!!!!!!!!!!!!!%f ROC=%f Using lamda=%-5.3f and mu=%-5.2f from calibrated query HMM %s. Note that HMMs need to be recalibrated when changing HMM-HMM alignment options.Using score distribution parameters lamda and mu from database HMMs Combining score distribution parameters lamda and mu from query and database HMMsScore: %7.1f lamda: %7.1f mu: %7.1f P-values: query-calibrated: %8.2G template-calibrated: %8.2G geometric mean: %8.2G Warning: some template HMM (e.g. %s) are not calibrated. Using query calibration. A3Mhhalign.cpp%s:%s:%d: strlen(prof1)=%d, strlen(prof2)=%d -- Nothing to align! %s:%s:%d: switch to Viterbi (qL=%d, tL=%d, MAC-RAM=%d )WARNING: Not sufficient memory to realign with MAC algorithm. Using Viterbi algorithm.%s:%s:%d: Problem Reading/Preparing q-profile (len=%d) %s:%s:%d: Problem Reading/Preparing t-profile (len=%d) %s:%s:%d: Problem Reading/Preparing profiles (len(q)=%d/len(t)=%d) Using maximum accuracy (MAC) alignment algorithm ...Using Viterbi algorithm ...Using stochastic sampling algorithm ... What alignment algorithm are we using??%s:%s:%d: cannot complete hit.Forward %s:%s:%d: cannot complete hit.backward Printing alignments in format to %s:%s:%d: Could not print alignments Aligned %s with %s: Score = %-7.2f P-value = %-7.2g Aligned %s with %s (rank %i): Score = %-7.2f P-value = %-7.2g nan after MACnan after backtraceWARNING from : could not open 'TARGET FAMILY REL LEN COL LOG-PVA S-AASS PROBAB SCORE %*.*e%#*.*f%-10s %-10s %1i %3i %3i %s %7.2f %6.2f %7.2f Exclude SCOP superfamily %s ptr_in_fam='%s' Exclude hit %s (family %s contains %s) %3i %7.3f %7.3f Fitting correlation coefficient for HHblast... iter corr offset logLikelihood tol%3i %-7.3f %-7.2f %-7.3f %-7.1E HHblast correlation=%-6.3f score offset=%-6.3f Reading in weights file Error: %s could not be opened: (N_searched=%i) fopenSkipping caclulation of transitive P-values Error: Number %i of HMMs in weight file is different from number %i of HMMs in searched databases. Calculating transitive P-values for %i HMMs Transform P-values to Z-scores Zmax = %6.2f Zmin = %6.2f Error: no index found in weights file for domain %s Excluded fold %s from fitting to Ztq Calculate inverse of covariance submatrix Covariance matrix Inverse covariance matrix Calculate Ztq vector of transitive Z-scores Calculate Zrq vector of transitive Z-scores Calculate mean and standard deviation of Ztq %4i %-10.10s Zq=%6.2f Ztq=%6.2f Zrq=%6.2f -> Zqtot=%6.2f mu(Ztq)=%6.3f sigma(Ztq)=%6.2f Normalize Ztq and calculate P1-values w[%4i] = %-8.5f %4i %-10.10s Zq=%6.2f Ztq=%6.2f Zrq=%6.2f -> Zqtot=%6.2f count number of profiles in each family and families in each superfamily ...%-3i HMMs from %i families and %i superfamilies searched. Found %i hits find %i best-scoring superfamilies to exclude from first fit ... find best-scoring superfamilies to exclude from second fit ... generate scores and weights array for ML fitting ...%i hits used for score distribution Fitting to EVD by maximum likelihood... iter lamda mu -log(P)/N tol Blank name in A2M file %s (line %d) a2m.c%s:%s:%d: could not malloc %d char for buffer>%s %saligneval.calignio.c%*s%-10.10s %5d %s %5d %*s %s CLUSTALmultiple sequence alignment .*:Parse failed at line %d, file %s: possibly using spaces as gapsclustal.c%s:%s:%d: could not malloc %d int for residue countCLUSTAL O(%s) multiple sequence alignment %s%*s %s %d %s%*s %s CSAATVSAGSTNKSTPASGNDSNDEQKNDEQHKNEQHRKFVLIMHFYSTANEQKNHQKNDEQQHRKMILVMILFHYFYWcluster.cAllocPhylo() failed%s:%.5f); ):%.5finteriorInterior node %d (code %d) Parent: %d (code %d) Left: %d (%s) %f Right: %d (%s) %f Height: %f Includes:%d seqs file.c%s%c%s%s.%s:gki.cbad primelevel in gki_alloc()Total keys: %d Hash table size: %d Average occupancy: %.1f Unoccupied slots: %d Most in one slot: %d Least in one slot: %d regexp(3): %s too many ()unterminated ()unmatched ()internal error: junk on endinvalid [] rangeunmatched []internal error: \0|) unexpected?+* follows nothingtrailing \^$.[()|?+*\internal error: strcspn 0*+ operand could be emptynested *?+NULL argument to sqd_regcompregexp too bigout of spacecorrupted pointersinternal error: bad call of regrepeatregexp corruptionNULL argument to sqd_regexeccorrupted regexpStrparse(): ntok must be <= %dregexp compilation failed.hsregex.cNULL parameter to sqd_regsubdamaged regexpdamaged match stringmsa.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 %sParse error: #=GR CO annotation for %s: length %d, expected %d in alignment %s%s: file does not existfilename > 255 char in MSAFileOpen()%s.ssiCan't autodetect alignment file format from a stdin or gzip pipeFile %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. Can't determine format of multiple alignment file %sMSAFILE corrupted: bad format indexcan't write. no such alignment format %d ..^.+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 squid.msfmsf.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(). %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 file#=CSselex.c#=SAParse error in ReadSELEX()#=ID#=DEParse error in #=GA line in ReadSELEX()#=TCParse error in #=TC line in ReadSELEX()#=NCParse error in #=NC line in ReadSELEX()#=SQParse 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.:: TAB characters will corrupt a SELEX alignment! Please remove them first.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 FATAL: PANIC [%s line %d] Unusual error//sqio.c LOCUS///ENTRY SeqfilePosition() failed: in a nonrewindable data file or streamSSISetFilePosition failed, but that shouldn't happen.SSIGetFilePosition() failedSeqfileRewind() failed: in a nonrewindable data file or streamInvalid flag %d to SetSeqinfoString()ACGTUNRYMKSWHBVDacgtunrymkswhbvd ; DNA sequence, DEFINITIONACCESSIONVERSIONORIGINLOCUS File %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 --infmt . ID AC ; DE SQTITLESEQUENCE>>>>([^ ]+) .+2BIT +Len: ([0-9]+)>>>>([^ ]+) .+ASCII +Len: [0-9]+bogus GCGdata format? %smalloc failedfread failed Length: EFIPQZABCDEFGHIKLMNPQRSTVWXYZ*ACGTUN>>>>Len: !!AA_SEQUENCE!!NA_SEQUENCE!!AA_MULTIPLE_ALIGNMENT!!NA_MULTIPLE_ALIGNMENT#=AU#=AC#=GA#=SS#=RFENTRY MSF:Check:LOCUS ORIGIN ID SQ #%Sequence file contains no data Check: [STDIN]^.*\.gz$filename > 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 %s>%s %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 %s%s FASTAFAVIENNAVIEGENBANKEMBLGCGGCGDATARAWIGSTRIDERIDRAWZUKERPIRSQUIDSTOCKHOLMSTSTKSELEXMSFCLUA2MPHYLIPPHYEPSunknownViennaGenbankGCG data libraryrawIntelligeneticsMacStriderIdraw PostscriptZukerStockholmClustala2mPhylipBad code passed to MSAFormat2String()sre_math.cIncompleteGamma(): a must be > 0IncompleteGamma(): x must be >= 0IncompleteGamma(): failed to converge using continued fraction approxIncompleteGamma(): failed to converge using series approxmalloc of %ld bytes failed: file %s line %drealloc of %ld bytes failed: file %s line %dsre_string.c%s %u %lu %lu %lu %s %u %llu %llu %lu %s %s %s %d %lu %lu %lu %s %d %llu %llu %lu wbCan't switch to 64-bit SSI index mode on this system, sorry; I don't have 64-bit file offset functions available. env LC_ALL=POSIX sort -o %s %s Can't create a 64-bit SSI index on this system, sorry; I don't have 64-bit file offset functions available. tmp.ssi.1tmp.ssi.2ok (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 codefailed to turn external sorting on.stack.cMemory allocation failure at %s line %dIDACDEAUGANCTCWTSS_consSA_consRFSSstockholm.cSACO# 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 # STOCKHOLM 1.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 %s# DUBLIN 1.File %s doesn't appear to be in Dublin format. Dublin format parse error: line %d of file %s while reading alignment %sCPU Time: %02d:%02d:%02d.%02d%.2fu %.2fs %s %02d:%02d:%02dElapsed: %s 0x0Xbasic_string::_S_construct null not validCompleted iteration #, cost=...Completed run: cost= ( seconds)Aggregate info over runs: Cost: min= average= max= Time: min=Running k-means++...Done preprocessing...k >= 1KMeans.cppcenters != 0Running k-means...centers != 0 && unused_centers != 0bound_p1 != 0 && bound_p2 != 0KmTree.cppsize1 >= 1 && size1 <= last_index - first_indexcenter != 0node_data_ != 0 && point_indices_ != 0bound_v1 != 0 && bound_v2 != 0new_candidates != 0sums != 0 && counts != 0 && candidates != 0bad_center != 0dist_sq != 0ASSERTION FAILURE, line --,[]| [-%c -%c[%c%c [%s] [%s] [%s] [%s]... %-20s %s , %-25s %s: too many errors to displayinsufficent memoryunexpected argument "%s"option "%s" requires an argumentinvalid option "%s"invalid option "-%c"%s: missing option %s: extraneous option missing option excess option invalid argument "%s" to option integer overflow at option (%s is too large) KBMBGBunknown error at "%s" std::bad_allocstd::bad_caststd::bad_typeid%ld_GLOBAL_(anonymous namespace)[abi:::{default arg#}::JArray[]vtable for VTT for construction vtable for -in-typeinfo for typeinfo name for typeinfo fn for non-virtual thunk to virtual thunk to covariant return thunk to java Class for guard variable for TLS init function for TLS wrapper function for reference temporary # for hidden alias for transaction clone for non-transaction clone for _Sat _Accum_Fractoperatoroperator adgsst>(clixqu : new ulllulljava resource decltype (this{parm#global constructors keyed to global destructors keyed to {lambda()#{unnamed type# [clone restrict volatile const&&complex imaginary ::* __vector(string literalstdlidtptstd::allocatorallocatorstd::basic_stringbasic_stringstd::stringstd::basic_string, std::allocator >std::istreamstd::basic_istream >basic_istreamstd::ostreamstd::basic_ostream >basic_ostreamstd::iostreamstd::basic_iostream >basic_iostreamaN&=aSaa&anatalignof azccconst_cast()cmco~dV/=dadelete[] dcdynamic_castdedldelete ds.*dv/eO^=eo^eq==ge>=gtlS<<=le<=operator"" ls<<lt<mI-=mL*=mimlmmnanew[]ne!=ngnt!nwnewoR|=oo||orpL+=pl+pm->*pp++ps->?rM%=rS>>=rcreinterpret_castrm%rs>>scstatic_castsizeof sztrthrowtwthrow signed charboolbooleancharbytedoublelong doublefloat__float128unsigned charintunsigned intunsignedlongunsigned long__int128unsigned __int128shortunsigned shortvoidwchar_tlong longunsigned long longdecimal32decimal64decimal128halfchar16_tchar32_tdecltype(nullptr)std::exceptionstd::bad_exception__gnu_cxx::__concurrence_broadcast_error__gnu_cxx::__concurrence_wait_errorpure virtual method called deleted virtual method called terminate called recursively terminate called after throwing an instance of 'terminate called without an active exception what(): a+br+w+a+abr+bw+blocale::facet::_S_create_c_locale name not validLC_CTYPELC_NUMERICLC_TIMELC_COLLATELC_MONETARYLC_MESSAGESCPOSIXbasic_ios::clearios_base::_M_grow_words is not validios_base::_M_grow_words allocation failed%.*Lf%m/%d/%y%H:%M%H:%M:%S__gnu_cxx::__concurrence_lock_error__gnu_cxx::__concurrence_unlock_errorlocale::_S_normalize_category category not foundlocale::_Impl::_M_replace_facet-+xX0123456789abcdef0123456789ABCDEF-+xX0123456789abcdefABCDEF-0123456789GMTHSTAKSTPSTMSTCSTESTASTNSTCETISTEETJST*AMPMSundayMondayTuesdayWednesdayThursdayFridaySaturdaySunMonTueWedThuFriSatJanuaryFebruaryMarchAprilMayJuneJulyAugustSeptemberOctoberNovemberDecemberJanFebMarAprJunJulAugSepOctNovDecbasic_filebuf::xsgetn error reading the filebasic_filebuf::underflow codecvt::max_length() is not validbasic_filebuf::underflow incomplete character in filebasic_filebuf::underflow invalid byte sequence in filebasic_filebuf::underflow error reading the filebasic_filebuf::_M_convert_to_external conversion errorstd::future_errorbad_function_callfutureBroken promiseFuture already retrievedPromise already satisfiedNo associated stateUnknown errorregex_errorgenericsystembasic_string::atbasic_string::copybasic_string::comparebasic_string::_S_createbasic_string::erasebasic_string::_M_replace_auxbasic_string::insertbasic_string::replacebasic_string::assignbasic_string::appendbasic_string::resizebasic_string::basic_stringbasic_string::substrOut of memory allocating %lu bytesXtruefalseInvalid value for environment variable %sOMP_SCHEDULEstaticdynamicguidedUnknown value for environment variable OMP_SCHEDULEInvalid value for chunk size in environment variable OMP_SCHEDULEOMP_DYNAMICOMP_NESTEDOMP_PROC_BINDOMP_MAX_ACTIVE_LEVELSOMP_THREAD_LIMITOMP_NUM_THREADSOut of memory while trying to parse environment variable %sGOMP_CPU_AFFINITYnot enough memory to store GOMP_CPU_AFFINITY listInvalid value for enviroment variable GOMP_CPU_AFFINITYOMP_WAIT_POLICYactivepassiveInvalid value for environment variable OMP_WAIT_POLICYGOMP_SPINCOUNTinfiniteinfinityOMP_STACKSIZEGOMP_STACKSIZEStack size less than minimum of %lukStack size larger than system limitStack size change failed: %s libgomp: Thread creation failed: %scould not create thread pool destructor.__eh_frame__TEXTConvertOldCmdlineMyMainParseCommandLineFreeUserOptsAlignAlignmentOrderSequentialAlignmentOrderAlnToHMMAlnToHMMFileAlnToHHMFileFreeAlnOptsHHalignWrapperPileUpPosteriorProbabilitiesPrepareAlignmentReAttachLeadingGapspair_alignKTuplePairDistMbedBisectingKmeansSeedSelectionSeqToVecNewKMeansResultFreeKMeansResult)\@㥛?^i?/?Il?&?? #?-??Ԉ??@;?????????? ?Q>B`E?X?|?%@/]??Sc>!"@Ԉ?M?">+?/??!>/?¥?-?Zd?H???????????%?>o#?+G??m@R??N>L71@w?6? ף>V ?r??q=>ף?? ? ??1@??????????>O ?.? ף?H@!2??V->{>@X9t?V?Ƌ>5^>??X9>W??B`?5^?P????????????(>S>x ?&?H@??=tK@X?S?xi>t>??Nb>7??ף?#??A??????????#?>j>x>Zd{?33@>?`=-]@2?>-2>sh>-??rh>??I?+??G??????????F @/>>S>J?l?ף>?ʡ=hm@?;ߏ>'1>9H>Zd??&1>~>?r@J ?(???????????`@+>D>B`e>H?p?Zd;>?Y=@T>M>t=Nb>Ck??d;=>@t@`?u?7??????????*@=9=t>}?>P?`=?h<@sh>l=X94=q=ˡ??Y=L>V@j@@+???????????=@t<jC<? #<‘@F=/< #?<=/$@/?V @->|>EDDDDDDDDDDDDDDDDDDDDEDDDDDDDDDDDDDDDDDDDDEDDDDDDDDDDDDDDDDDDDDEEDDDDDDDDDDDDDDDDDDEEDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDpFD/DaDaDDDDDDDDDDDDDDDDDzECDDDDDDDDDDDDDDDDD/DCZE/D/DDDDDDDDDDDDDDDDaDD/D F FDDDDDDDDDDDDDDDaDD/D F FDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDDD;p;;-;o;947;k;o;o:RI:l :㥛<-:RI:9RI9947:RI:o:RI9 #;d;47:;4:47:RI:RI:o:o:RI:k:47:|0;d;47:o:٬<' ;k:47:k:RI947:RI:o:947:RI:RI:RI99 <;o; >;RI;o::d*;^;o::' ;d*;47:o:4:pΈ; #;' ;.;RI9^;'<Ǻ;:|0;RI;47:d::3"=o:d:4:k:Q9o:d:k:RI<_)K;RI:k:-:RI:Q:RI:d:RI:w<;;d:4:::l :o;k:j<<=Q;_);RI;RI;o:D;o;RI;RI::RI;;{r;-::RI;D;Q:RI::u`<{r;:-;l :k:d:' ;-;47:|0;DX;;o:RI:d:RI;>Y<9RI9Q98Q9Q9Q99Q9947:RI9Q9k:8RI9RI9{;d:k:47:RI:9RI:Q:Q:::;o:RI:;9o:k:o:#9<.;:-:RI:4:-:::RI:D;;RI;RI:DX;g<_);o;_)K;47;k::;o=RI:d::-:RI9o:d:-:;B`e;:d:RI:Q:-:::47:B`e;;47;4::|0;T<:k:47:o:9Q:Q:k:o:-;';o: >;o;RI:k:Q:RI:47:RI::k:D; ;RI:RI:HP|<-;-:-::9-:l :l :RI:d:::o:47:M<_); #;Q;47;-:-;D;-;RI:' ; >;_)K;o:::5<$;' ;d*;-;o::RI; #;k: >;l y;d*;-:::u; #;KY;o::KY<{r< >;2< >;l :e;Q;' ;_)K;;pN<:47:47:k:_;k:47;$; >;-:l :-;;B`;47:o:RI9RI989o:Q:Q9o:k:o:Q9Q:RI99RI9t;l ::o:-:9o:4::RI:o;_)K;:o:Q;k::4:Q:;|;;:-;RI:4: #;47;Q:;o:-:+<4;B`e;47;^;d:' ;l y;;:DX;u;';o:|0;RI;;o;l :RI;RI;k::;47;o:|0;; #;o::o;KY;;o:47:Q99RI9947:-:Q9o:k:RI:Q947:9o:RI9|0;4:-;Q::9-:::o::t;:47:RI;-::4:k:-;4;_)K;-;|0;RI::d*;DX;RI:;p;{;D;:Q;:k;k;o:RI;<F`VE3EqE DEpE EEIEصE`E`D`DiEEECDhE`VE E E!EDERE@EEDPAE(E>DVDDEYEC@D@E3E EqEaECD8EOED DD3ED,DDE@HE[CDDqE!EaEFCE(EEE`DpEbED'D`E0E0pELCDD DDCCPEC DaDD@9DDDC@ DC@aDD;C&DDEEDEC`D4ED`D@D@ E+EDDD`D0E[CYD@DpERE8E(E D4E$FjE ED@DEEODUD E6EECD/E E@EOEEaDDjEFD@DP+EZE@9D@GDEpqEHEC@D EEEDED`D EDE`DEED`D@D@DEC[D`DIED D`D@9D@DD@D`DExF@DD EDDCEC DEصEPAEDpED@ E@DEP+EExF2FeE؂E E&E3EEDvE+F`E(E3EbED+EEZEE@DeE0E@mDsD0E1EEC`D@7E`D>DDDCDOD@9DDD؂E@mDDD@D9D DZCOD`E`DVD,D'D@ DDUD@GD`D E EsDDpE@%DVD@DzDE"EiEDD`ECD EE@DD&E0E@D@%D8FE@NE3C[D0EEEE0E@aD`D6EpqE@DD3E1E9DVDEaEpECDp(EEYE@HE0pED0EEHEECEEE D@D@NEpE FCDECC[CLC;C[CCCCCDCZCzD3CCC(E@DCD@DDD&DYDD@D[D DvE`DODE[DDD@DF0 EhE@EDDD@D/E E`DE+F@7E`E"E0Ep(EEC0 E4F  version 1.5.1.3 (November 2008)>G8@|=^$3eG?$@0 ?y8??333333???^/MtPd@Ytw?(F̱? 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