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HBHHǃƃƃHǃHǃHǃHǃHLbLID$HID$LzLHHPHH@H(H@HHHBHHDžHDžHDžHDžHDžHDžH(H@[L5QIFHDžL-IEHHH(HHZH5H@ZH@ZHH+HE11H@HPHLuHUHHPHHUHHEHL`HUHHEHHHLYLLYH`HI9HHH8HuHVYH}HI9PAHHH+HA9HHUHHHH9SHHHHYHLXHPHI9HHG3HX"fDH@XHH0HXdlH +HH+HHLHH(HHXHXHHBHHǃƃƃHǃHǃHǃHǃHMLbLID$HID$LzLHFHPHH@HHHBHHDžHDžHDžHDžHDžHDžH(H@zWL5IFHDžL-aIEHHH(HH\WH5H(PWH(\WHH+HE11H(HPHLuHUHH0HHUHHEHL@HUHHEHf.HHL8VLL'VH@HI97HH1H8HuHVeVH}HI9AHH H+HA9HHUHHHHH9SHHHHUHLoUH0HI9HHG3H.U"fDH(LUHchHHcdHVIH\HHEHE1HUHEHxHpT1HpH HxHHEHL}LuLm xL⋵hH0NHUHT$8HHHD$0H HT$(HHD$ HHT$L|$Lt$L,$xMLXdhlH0;TYTpx]UME*L*UEpH0pHx[A\A]A^A_HLhSHLTSLLLrCCL+C.LH$Ld$Ll$Lt$fA$CfDL5IH=AfDUHSHHHHֈ$H AHH[ÐUH AfDUHH]LeLmLuL}H@IIIHWH;WtQHt HBHHWHHIT$IHWL)HH)LtBI]H]LeLmLuL}fH+HHH9HH HEHH9|@II4$LH)HHALHtIHLzI\$L)HLLAI<$Htw@M4$IID$HUIID$2f.HH9wH<H}dH= @?UHDGE~BH~*fW11^\YXHD9uYf(XF *fWYf(XF f.UHDE1E9HLDIcHAfWf(f(E1E1*BBX\YXAIA9tECB \f(YXf.wBB\\YXAIA9uXE1f.AD@UHH]LeLmH IHAԉS8Hv(Ht'Hs0DLH]LeLmfDH]LeLmfUHAWAVAUATSHIHAIMNjF8xDHVHvEAHSHsDK8ELLtH{(tZHs(MLDLEHs0MLDLfXEHC(P8HC0;P8t?C8H[A\A]A^A_AT$S8HcIHLH[A\A]A^A_rtS8H[A\A]A^A_DHLDSDA9IcL MfWAt$DHIAC>AuHcH<DD)ʉAA ʉHcIM 4HcHIuHLM=AEfW҅~afWE11AuMM A9HHIEfWɅ~ 11A\YXH9uA ~XAHE9E}UZ=*^UYAE~fWAXf.s9~AX HJf.s~H1AuHcIA$EED1}19t1L}tH[A\A]A^A_D{HED1 u1EH[A\A]A^A_øH[A\A]A^A_DfDUHAWAVAUATSHIIMAIIA$1p u+t4E-uIA$E0t(M.1H[A\A]A^A_IA$E0uA|$1A19uI\$ULHhHI9tHcEHf.UHH]LeLmLuL}H@IHG`A;G,HLmȹXLHILeI9IH9EAH5LtoI H=?I Eu#AG`HcIWhD4AG`DH]LeLmLuL}G`IfH}H5PtTIH=vfDAIgOLLIL;etSLeH}H5tIFHwIH}H5ABLLYIL;eu LLl IAL;elUHG`UHO`;O,tHt HcHWhH4AG`1DUHG`;G(UHAWAVAUATSHIIIALMA9ȉAMHcH%@%B%D%F%H%J%L%N%P%R%T%V%X%Z%\%^%`%b%d%f%h%j%l%n%p%r%t%v%x%z%|%~%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%¯%į%Ư%ȯ%ʯ%̯%ί%Я%ү%ԯ%֯%د%گ%ܯ%ޯ%%%%%%%%%%%%%%%%%%%%%% % %%%%%%%%%% %"%$%&%(%*%,%.%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%|%~%%%%%%%Out of memory allocating %lu bytestruefalseXInvalid value for environment variable %sOMP_SCHEDULEstaticdynamicguidedUnknown value for environment variable OMP_SCHEDULEInvalid value for chunk size in environment variable OMP_SCHEDULEOMP_DYNAMICOMP_NESTEDOMP_NUM_THREADSGOMP_STACKSIZEStack size less than minimum of %lukStack size larger than system limitStack size change failed: %s libgomp: Thread creation failed: %s=INFILE-iPROFILE1--profile1PROFILE2--profile2HELPCHECK-hFULLHELPALIGNINTERACTIVEQUICKTREETYPE-tOUTFILE-oOUTPUT--outfmtMAXSEQLEN--maxseqlenQUIETNEWTREE--guidetree-outUSETREE--guidetree-inSEQUENCESWARNING: %s: %s WARNING: Unsupported old command line option '%s' will be ignored WARNING: Invalid old command line optionWARNING: The ALIGN option is default in Clustal OmegaWARNING: There is no interactive command-line menu in Clustal OmegaWARNING: The QUICKTREE (i.e. k-tuple distance) option is default in Clustal OmegaWARNING: The QUIET option is default in Clustal Omega-v--forceWARNING: Your old-style command-line options were converted to: clustal.aln--outfmt=clustalConvertOldCmdlineNo sequence input was provided. For more information try: --helpCan't align two profile alignments AND a 'normal' sequence fileGot a second profile, but no first one. Alignment and log messages would get mixed up.You requested alignment output to stdout and verbose logging.%s %sDistance Matrix output not possible in mBed mode. Sequence Input:Multiple sequence input file (- for stdin){,-}in,infileiHMM input fileshmm-inDealign input sequencesdealignForce a sequence type (default: auto){Protein,RNA,DNA}seqtypetPre-aligned multiple sequence file (aligned columns will be kept fix)profile1,p1profile2,p2 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-outUse 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-iterClustering method for guide tree{UPGMA}clusteringc Alignment Output:Multiple sequence alignment output file (default: stdout){file,-}out,outfileoMSA output file format (default: fasta){a2m=fa[sta],clu[stal],msf,phy[lip],selex,st[ockholm],vie[nna]}outfmt Iteration:Number of (combined guide-tree/HMM) iterationsiterations,iterMaximum number 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 usethreadsLog 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)DeshilHollesEamus1.0.3Clustal Omega%s - %s (%s) Check http://www.clustal.org 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'.proteinrnadnaUnknown sequence type '%s'File '%s' does not exist.ktupleUnknown pairdist method '%s'upgmaUnknown guide-tree clustering method '%s'Automatic iteration not supported at the moment.Unknown output format '%s'Changing number of threads to %d doesn't make sense.Couldn't iteration parameter: %soption: seq-in = %s option: dealign = %d option: profile1 = %s option: profile2 = %s option: max-num-seq = %d option: max-seq-len = %d option: aln-out-file = %s option: aln-out-format = %s option: force-file-overwrite = %d option: threads = %d option: logFile = %s Reading sequence file '%s' failedsFile '%s' contains %d sequence%s, nothing to alignDealigning 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 exitParseCommandLineFreeUserOptsSetting 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.Read 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.Performing profile/profile alignmentAlignment score is = %foption: auto-options = %d (null)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: 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 Have only two sequences: No need to compute pairwise score and compute a tree.Reading guide-tree from %sReading of guide tree %s failed.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 FIXME: 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=%dUsing %d threadsSequences 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 anywayCouldn't exec %sHMMER hmmbuild -hCould 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 > %sInternal error: Unknown Hmmer version %dUsing HMMER version %d to calculate a new HMM./tmp/clustalo-hmm-iter_XXXXXXAlnToHMMFile() on %s failed.Processing of HMM file %s failedSep 14 2011version %s; code-name '%s'; build date %sprint 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 continueAlignment score for first alignment = %fReached maximum number of HMM and guide-tree iterationsIteration step %d out of %dIteration step %d out of Skipping guide-tree iteration at iteration step %d (reached maximum)Couldn'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)AlignAlignmentOrderSequentialAlignmentOrderAlnToHMMAlnToHMMFileAlnToHHMFileFreeAlnOptsin seq %d re-translated %d residue codes (%d true, %d case)inconsistency in un/aligned sequence %d >%s >%s FIXME: Using only first of %u HMMs (needs implementation)Sequence type is %s. HHalign has only been tested on protein.Dealigning aligned sequences (inside %s)Progressive alignment progressmerge 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 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, even Viterbi did not work hh-error-code=%d (mac-ram=%d) %scould not perform alignment -- bailing out %s:%s:%d: 2nd attempt workednode %3d, #leaves=%d: %d,Alignment scores with HMM:%2d: %f HHalignWrapperPrepareAlignmentReAttachLeadingGapsInternal error in %s: Unknown sequence type.Unknown character in seq '%s'(Partial alignment)K-tuple distance for sequence pair %d:%d = %lgABCDEFGHIKLMNPQRSTUVWXYZ-ACGTUN-KTuplePairDistpair_alignFORCED DEBUG: FATAL: CRITICAL ERROR: ERROR: WARNING: 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 %dCould not compute pairwise distances for mbed.Skipping 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 %dSomething went wrong during seed selection for mbedCould not convert sequences into vectors for mbedmBed created %u cluster/s (with a minimum of %d and a soft maximum of %d sequences each)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 writingMbedBisectingKmeansSeedSelectionSeqToVecNewKMeansResultFreeKMeansResultNULL!=treemuscle_tree.ctree!=NULLuNodeIndex1 < tree->m_uNodeCount && uNodeIndex2 < tree->m_uNodeCountIsEdge(uNodeIndex1, uNodeIndex2, tree)tree->m_uNeighbor3[uNodeIndex1] == uNodeIndex2tree->m_uNeighbor3[uNodeIndex2] == uNodeIndex1NULL != treetree->m_bRooted && uNodeIndex < tree->m_uNodeCountuNodeIndex < tree->m_uNodeCountNULL != tree->m_uNeighbor1NULL != tree->m_uNeighbor2NULL != tree->m_uNeighbor3uNodeIndex < prTree->m_uNodeCountInternal error in %s: sub=%uuNodeIndex1 < tree->m_uNodeCountuNodeIndex2 < tree->m_uNodeCountMissing edge length in tree %u-%uAssertAreNeighbors(%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=%.3g%sungetc failedEnd-of-file skipping white spacefgetc reached end of fileTree::GetToken: input buffer too small, token so far='%s'():;,Tree::GetToken, invalid TT=%uValidateNode(%u), %u nodesTree::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 mismatchInternal error: node index out of rangeIsLeaf(uNodeIndex, 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] %stree 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)IsRooted(tree), :%g( ; FIXME: output of unrooted muscle trees not implementedNULL!=prDstTreeNULL!=prSrcTreeuDstTreeReplaceNodeIndex < prDstTree->m_uNodeCountIsLeaf(uDstTreeReplaceNodeIndex, prDstTree)IsRooted(prDstTree) && IsRooted(prSrcTree)AppendTreeAppendTreeExpandCacheExpandCacheGetRootNodeIndexSetLeafIdGetNeighborGetNeighborGetNodeCountGetLeafCountAppendBranchAppendBranchMuscleTreeFromFileTreeZeroUnrootFromFileSetLeafNameSetEdgeLengthTreeValidateValidateNodeGetNeighborCountAssertAreNeighborsHasEdgeLengthGetEdgeLengthGetParentIsRootIsLeafMuscleTreeToFileTreeToFileNodeRootedInitCacheFreeMuscleTreeFreeMuscleTreeIsRootedNextDepthFirstNodeFirstDepthFirstNodeGetLeafNameGetLeafIdGetRightGetLeftTriangleSubscript(%u,%u) %uv < (g_uLeafCount*(g_uLeafCount - 1))/2muscle_upgma.cdistmat->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 != uNewNearestNeighborMuscleUpgma2MuscleUpgma2TriangleSubscriptSequences need to be aligned (%s)Using Kimura distance corretion which includes Dayhoff substitution table lookup for non-protein sequencesPairwise distance calculation progresspair_dist.cInternal error in %s:%sAligned distance for sequence pair %d:%d= %lgFIXME: reading of distance matrix from file not implementedCalculating 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 %sPairDistancesSquidIdPairDistKimuraCorrection%s done. CPU time: %s: %lu %%%s (%lu out of %lu)FreeProgressNewProgressProteinUNKNOWNDNARNAInternal error in %sWill never get heresqinfo->name = %ssqinfo->id = %ssqinfo->acc = %ssqinfo->desc = %ssqinfo->len = %dsqinfo->start = %dsqinfo->stop = %dsqinfo->olen = %dsqinfo->type = %dsqinfo->ss = %ssqinfo->sa = %sUnknown output format chosenCould not open file %s for writinginvalid output format should have been detected beforeinternal error: %sAlignment written to %sCannot 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%% FIXME: This modifies sequence ordering. Might not be what user wants. Will change output order as wellWas asked to add 0 sequencesJoining sequences of different type^.*\.gz$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=%sACDEFGHIKLMNPQRSTVWYACGTACGURead %d sequences (type: %s) from %sJoinMSeqsAddSeqSortMSeqByLengthFreeMSeqCopyMSeqNewMSeqReadSequencesSeqTypeToStrShuffleMSeqAliStatsymmatrix.cCouldn't allocate memory (%s|%s) WARNING: Reading of distance matrix from file not thoroughly tested! WARNING: Assuming same order of sequences in sequence file and distance matrix file (matching of labels not implemented) ERROR: 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 %s%lfCouldn't parse float from entry '%s' expected %d seqs, but only parsed %d One of the provided arguments is empty or NULL (print_matrix) Couldn't open %s for writing.%u %u x %u %-*s %fSymMatrixReadNewSymMatrixSequence 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)MuscleTreeFromFile failedUser tree must be rootedUser tree does not match input sequencesLabel '%s' in tree could not be found in sequence namestree logging...wCouldn't open tree-file '%s' for writing. SkippingGuide tree written to %sTraverseTreeGuideTreeFromFileGuideTreeUpgmarBad call to CkFree from %s:%d (pointer was NULL) FATAL: Out of memory (requested from %s:%d) Out of memory (requested from %s:%d) Couldn't close temporily created file %s. Expect trouble...Removing of temporarily created file %s failed. Expect trouble...Internal error: unknown order %cQSortAndTrackIndexRandomUniqueIntArrayPermutationArrayCkStrdupUsing the BLOSUM%2i matrix Function substr: >1000 chars to copy. Exiting.Warning from hash.C: key=NULLhhfunc-C.h%s:%s:%d: WARNING -- Background Pseudocounts point to NULL this is not intended - don't add background but CONTINUE %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=%4i %4i:%6.3f >%s %1c 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 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 HHHHHNeutralized His-tag at position %i start:%i end:%i EQKLISEEDLNeutralized C-myc-tag at position %i DYKDDDDKNeutralized FLAG-tag at position %i WARNING: maximum likelihood fit of score distribution did not converge. %3i %-7.3f %-7.3f %-12.8f %-9.3E Col SS II%3i %c %2i %*.*e%#*.*fProbab=%-.2f E-value=%-.2g Score=%-.2f Aligned_cols=%i Identities=%i%% Similarity=%-.3f Sum_probs=%.1f Score %3i %2i: %5.2f Template=%-12.12s i=%-4i j=%-4i score=%6.3f hhalignment-C.h%s:%d: Arena[%d]=NULL, cnt=%d %s:%s:%d: profile has no leading and/or trailing residues (h=%d:t=%d:#=%d) Q %-*.*s Q %-*.*s %4i %4i (%i) %*.*s T %-*.*s %4i T %-*.*s Transitive score Ztq: mu=%8.3g sigma=%8.3g Bwd scale %3i %3i: %9.3G %7.4f Post scale Forward total probability ratio: %8.3G hhhit-C.h%s:%s:%d: Backward score is %g %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: B_MM[%d][%d]=%g, B_MM[%d][%d]=%g, B_MM[%d][%d]=%g Fwd scale %s:%s:%d: Forward score is %g, Pforward is %g %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) Error: Di=%i: n[%i][X[%i]]=0! (X[%i]=%i) Error: Ii=%i: n[%i][X[%i]]=0! (X[%i]=%i) k=%3i score=%6.2f 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->D%4i %1c %1c %1c %6.3f %6.3f %6.3f %6.3f %6.3f %1i %2i %1i nss_dssp=%i nss_pred=%i 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 HMMsWarning: some template HMM (e.g. %s) are not calibrated. Using query calibration. Score: %7.1f lamda: %7.1f mu: %7.1f P-values: query-calibrated: %8.2G template-calibrated: %8.2G geometric mean: %8.2G 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!!!!!!!!!!!!!!!!!!!!!!!!!!!!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 Error: sequences in do not all have the same number of columns, e.g. first sequence and sequence . . 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.>HOMEWarning: could not find ./.hhdefaults or Arguments read in from .hhdefaults:Warning: no default options for '' found in Argument: %s Error in hhutil-C.h: . Please report this bug to developers L is not set in AddSequence(): Memory overflow while creating ''. Please report this bug to developers 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 memoryError: unallowed state value %i occurred during backtracing at step %i, (i,j)=(%i,%i) space for HMM-HMM alignmentsNAME=%7.7s score=%7.3f score_ss=%7.3f step Q T i j state score T Q cf ss-score P_post Sum_post%4i %1c %1c %4i - %1c %4i %1c - %4i %4i %2i %7.1f %c %c %1i %7.1f %7.5f %7.2f step Q T i j state score T Q cf ss-score%4i %4i %2i %7.2f %c %c %1i %7.2f 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: %4.1f 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 %3i: %4.0f 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%4i %6.3f %6.3f %6.3f %6.3f %6.3f %6.3f array of names for sequences to display: could not open file '' stdout%f ROC=%f Query %s Match_columns %i No_of_seqs %i out of %i Neff %-4.1f Searched_HMMs %i Date %sCommand %s <%i characters> 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) a#%s a3mWriting A3M alignment to >%s %s Writing PSI-BLAST-formatted alignment to %-20.20s Writing alignment to : wrong format while reading file '. Command: ! ERROR when executing: HHNAMEReading 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: 'WARNING: invalid symbol '' at pos. in line '' of 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 WARNING: could not read line '' in HMM in 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 = 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[] 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 %): 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) ****************%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 Error: Writing transition pseudocounts in linear representation not allowed. Please report this error to the HHsearch developers. Writing HMM to HMMER2.0 [hhmake %s] NAME %s DESC %s LENG %i ALPH Amino RF yes CS yes MAP yes COM NSEQ %i DATE %sSSDSS %s SADSS %s SSPRD %s SSCNF %s XT %6i %6i %6i %6i %6i %6i %6i %6i NULT -4 -8455 NULE * %6iHMM %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 * * Recording calibration coefficients in EVD 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. HHsearch 1.5 FAM %s FILE %s LENG %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 # NULL * %i %1c M->M M->I M->D I->M I->I D->M D->D Neff Neff_I Neff_D %1c %-4i %-i 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: 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 %3i: sum=%5.3f 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 %i out of %i core alignment sequences passed filter ( out of sequences filtered by minimum score-per-column threshold of 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 hhhitlist-C.h%s:%s:%d: qt_ali.Build failed 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 rbError: %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 Covariance matrix w[%4i] = %-8.5f Calculate Ztq vector of transitive Z-scores Calculate Zrq vector of transitive Z-scores %4i %-10.10s Zq=%6.2f Ztq=%6.2f Zrq=%6.2f -> Zqtot=%6.2f Calculate mean and standard deviation of Ztq mu(Ztq)=%6.3f sigma(Ztq)=%6.2f Normalize Ztq and calculate P1-values %4i %-10.10s Zq=%6.2f Ztq=%6.2f Zrq=%6.2f -> Zqtot=%6.2f Calculate inverse of covariance submatrix Inverse covariance matrix 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 tolWARNING from : could not open 'TARGET FAMILY REL LEN COL LOG-PVA S-AASS PROBAB SCORE %-10s %-10s %1i %3i %3i %s %7.2f %6.2f %7.2f stdinsequences;No '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 Length =HMMERACC 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 STATS LOCALEFFNCOMPO NULL %6.3g Error: in HMM AminoNULTNULEWarning: some HMMs have been calibrated with HMMER's 'hmmcalibrate'. These calibrations will be ignored 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 is in A2M, A3M or FASTA format %s:%s:%d: FATAL problem infile = (%s), #seq = %d 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 hhalign.cpp%s:%s:%d: strlen(prof1)=%d, strlen(prof2)=%d -- Nothing to align! 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 nan after MACnan after backtraceFASTAA2MA3MPrinting 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 hhalignReadAndPrepareAddBackgroundFrequenciesPrintAlignmentsBackwardForwardTransferMergeMasterSlaveversion 1.5.1.3 (November 2008)ReadHMMer3ReadHMMer>%s %s%s Blank name in A2M file %s (line %d) aligneval.calignio.c%*s%-10.10s %5d %s %5d %*s %s CLUSTAL O(%s) multiple sequence alignment %-*s %s CLUSTAL .*:Parse failed at line %d, file %s: possibly using spaces as gapsSTANEQKNHQKNDEQQHRKMILVMILFHYFYWCSAATVSAGSTNKSTPASGNDSNDEQKNDEQHKNEQHRKFVLIMHFYInterior node %d (code %d) Parent: %d (code %d) interior Left: %d (%s) %f Right: %d (%s) %f Height: %f Includes:%d seqs cluster.c%s:%.5f); ):%.5fAllocPhylo() failed:%s%c%sfile.c%s.%sTotal keys: %d Hash table size: %d Average occupancy: %.1f Unoccupied slots: %d Most in one slot: %d Least in one slot: %d gki.cbad primelevel in gki_alloc()regexp(3): %s NULL parameter to sqd_regsubdamaged regexpdamaged match stringinternal error: bad call of regrepeatregexp corruptioncorrupted pointersNULL argument to sqd_regexeccorrupted regexptoo 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 spaceStrparse(): ntok must be <= %dregexp compilation failed.hsregex.cmsa.cFile %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 write. no such alignment format %d MSAFILE corrupted: bad format indexParse 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 %s failed to sre_strcat()%s.ssiCan't autodetect alignment file format from a stdin or gzip pipeCan't determine format of multiple alignment file %smsf.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 MSF:^.+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 %d %d %-10.10s%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 #=AC#=NC#=RFselex.c#=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 #=SACan't read a SELEX format alignment from a pipe, stdin, or gzip'ed fileParse 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.:: 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? PANIC [%s line %d] Unusual error FATAL: PhylipEPSunknownViennaGenbankEMBLGCGGCG data libraryrawIntelligeneticsMacStriderIdraw PostscriptZukerPIRSQUIDStockholmSELEXMSFClustala2mBad code passed to MSAFormat2String()FAVIENNAVIEGENBANKGCGDATARAWIGSTRIDERIDRAWZUKERSTOCKHOLMSTSTKCLUPHYLIPPHY>%s %s ACGTUNRYMKSWHBVDacgtunrymkswhbvd ///ENTRY//LOCUS>>>>Len: !!AA_SEQUENCE!!NA_SEQUENCEmultiple sequence alignment!!AA_MULTIPLE_ALIGNMENT!!NA_MULTIPLE_ALIGNMENT#=AU#=ID#=DE#=GA#=TC#=SQ#=SS#=CSENTRY ..Check: Check: LOCUS ORIGIN ID SQ #%Sequence file contains no datasqio.cInvalid flag %d to SetSeqinfoString()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 [STDIN]Can'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 %sSSIGetFilePosition() failedSeqfileRewind() failed: in a nonrewindable data file or streamSeqfilePosition() failed: in a nonrewindable data file or streamSSISetFilePosition failed, but that shouldn't happen. TITLEACCESSIONSEQUENCEDEFINITIONVERSIONORIGINLOCUS ; DNA sequence, 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 --informat . ID AC ; DE SQ>>>>([^ ]+) .+2BIT +Len: ([0-9]+)>>>>([^ ]+) .+ASCII +Len: [0-9]+bogus GCGdata format? %smalloc failedfread failed Length: EFIPQZABCDEFGHIKLMNPQRSTVWXYZ*ACGTUNsre_math.cIncompleteGamma(): a must be > 0IncompleteGamma(): x must be >= 0IncompleteGamma(): failed to converge using continued fraction approxIncompleteGamma(): failed to converge using series approxrealloc of %ld bytes failed: file %s line %dmalloc of %ld bytes failed: file %s line %dsre_string.csome problem with external sortingunrecognized codeok (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() failed%s %u %lu %lu %lu %s %u %llu %llu %lu %s %s failed to turn external sorting on.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.2%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 stack.cMemory allocation failure at %s line %d# 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. #=GFIDACDEAUGANCTC#=GSWT#=GCSS_consSA_consRF#=GRSSstockholm.cSAStockholm format parse error: line %d of file %s while reading alignment %sDidn't find // at end of alignment %s# STOCKHOLM 1.0 # %s #=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 %02d:%02d:%02d.%02d%02d:%02d:%02dCPU Time: %.2fu %s Elapsed: %s 0x0Xbasic_string::_S_construct NULL not validvector::_M_insert_auxAggregate info over runs: Cost: min= average= max= Time: min=Completed iteration #, cost=...Completed run: cost= ( seconds)Running k-means++...Done preprocessing...k >= 1KMeans.cppcenters != 0Running k-means...centers != 0 && unused_centers != 0dist_sq != 0KmTree.cppnew_candidates != 0sums != 0 && counts != 0 && candidates != 0bad_center != 0bound_p1 != 0 && bound_p2 != 0size1 >= 1 && size1 <= last_index - first_indexcenter != 0node_data_ != 0 && point_indices_ != 0bound_v1 != 0 && bound_v2 != 0ASSERTION FAILURE, line -%c [-%c%c[%c][--, [%s] [%s] [%s] [%s]..., %-25s %-20s %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) KBMBGB%s: unknown error at "%s" ?<o   !#$&(*+-/13579;=?ACEHJLOQSVX[]`behjmpsvy| !)09AJS]gr}3Mj(\?@@C?Y@?X?tՖR>Q? 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