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H ~wHc, Hc1 H%V,1Љ1‰ 11H V,1%1ȉ1[H ]fDuHߋ+ xH HHc,[@SH/. ~N H[ 1ЉV,1‰%1Љ1H*HH*H..YH[]u>Hߋ+t dfHHH H*XfH8 HHc,@SDH1 i  HH=DuHǃ p%H[fff.H SH f.H1ielƃq=puHǃ pH[eDAVIHH5QAUATUSH dH%(HD$1fHHLl$1H1AhHcLHI|5H)htYÃ~HitOH1Kf$Li@Bt$t$D$HL$dH3 %(uNH []A\A]A^ÐHHi뱋t$LD$H5mH=ifHHt.@khff.H5H@H5,@AUH5A ATIH=US1HeHHtHHcLHI<4H)gt"Á ~HH[]A\A]vhfDHhhHL[]A\A]ffDATIUHS t| pwF1f.HH@tk Ha1L&dy[]1A\H!HBH81cH듐HrfD HL1c[]A\fAUIATL UHS1Hdž dž HH@t+IH51H>ct1H[]A\A]@I H5Q1HcuA pvADž 0LD$ cD$ ffff.H=*.fH=)."fHH=).H=).@H=).@H=).@H).H5).@H5).@AWAVIH5fAUATIUHSHHbHIH51LLatH=H1DfH51LLatH=H1fH5c1HLatH=H1ed11RAAdII@HH5U1LLXau+IF$A9(ELD?ADuH=TveLdLAHL[]A\A]A^A_ d86cH=oTHH12effff.UH8SHMgHHHPHHHWHC0HA*HKS\C(\?^C H[]DSHH0sNH[af.ff.Gf.Gf.HG0ff.H0GAGf.G f.HfWY$$-T\$D$f.v"]d ?f.w/YOHff.vH=DcfOHHfWYG$$-+T\$D$f.v!c \?f.w.YVOHÐf.vH=CD9cfOHH6H?bDSH`@@1@Ht H@t 1HfGtHH= H޹ CH dCXHC@dHCP[ÐH{@_@h@1HfW@WHDfffff.SHHPHt._H{@Ht _HHaHߺ`uC@uU@ug1Ht Ht 1HfGt[DH_@tf1HfO@tDHfAWAVAUATUSHXHHt$H>JHD$HPLxH4HML|$IHD$1MH1Ld$@A@IIWHt;H=WE1MHO tI}^EtICMuEL|$9EHD9uXH]PHL$HHHyI|$ALl$1HD$MH|$(H|$0H)L$LH|$f.Hu@H=E1MHHHHE@J0L9L} HE@Ll$ J0Lt$(}Dl$LItA)Հ>xZAUHHc[_Icͺ 1D H]HT$Hމ5iHcD$0HHcD$DH=E1MHIL tTHcT$@HL^HcD$@T$HHHcA<#ZH2LLHfDAUItHHc]Icͺ1D Hu\HLLu&HfDHLLvuh"HifDHD$HX[]A\A]A^A_H}PDuXIcdHEPH5H}@Hc]HHdD9uXHE@ H!LLu'H1H=r1c]197/u(9Wu9O DfDH>1f.ATIUStfHZH1fDHAt[HӉDQ uHcI4t/IT4HHBtDA u[]A\f]1[]A\fD[]A\fDATIUSHH [HHHdZH9$t=UuHH9v"H[]A\DA$H[]A\úf.ATIUSHHZH HHYH9$t=UuHH9v"H[]A\DA$H[]A\úf.ATIUSHH ZH HHdYH9$tUuI$H[]A\úATIUSHHYHHHi[H9$t0E"uA$1H[]A\f.tH[]A\øfff.ATIUSHHMYHHHZH9$t@E"u+fWɸf.wf.<5wA$1H[]A\ÐtH[]A\øfff.ATIUHSXHHfuA$[]A\ffffff.ATIUHSXHHPfuf.5v[]A\fD[]A$A\DSHHHcLYHvH|$H|$nxHKHHS1H[ATUHSHHFF? H8WH<$H9t}tf<.urHo HHWCH$H9tRt;.uFHh HHVCH$H9t&8H[]A\fH1[]A\DH[]A\fUIcHAWAVMAUATSHHLm(HEHH}HuHHUHMH)MDELDE~HU1LxSHEH8HXHAE1:I E1HUH}HEHHID$H?t|MILHUȹL&mxHcID8uHEHUN|HEI?H4HEЅHUtI MHUH}HEv@E~aEM1MLm D`IHL9t7A|tA<uI HE1HUH}HEL9uDHe[A\A]A^A_]Ðf.SHVTHX[f AWAVAUATUHSHL/H4$MtBA~;H1HHD$fDH$HcL<DA?AՅuIA9H[]A\A]A^A_fA9~D{E9~*H$IcL4DAIE9t A>AՅuHcuD);E}xA9HEH $LcB<;JLD$IHcuHE~H}zL9@<0uHcEHUE9D!H[]A\A]A^A_f.H}HcE\A9HEHcur0@AWAAVIAUIATL%!UH-!SL)1HH PHtLLDAHH9uH[]A\A]A^A_ff.HH Usage: centrimo [options] + Options: --o output directory; default: 'centrimo_out' --oc allow overwriting; default: 'centrimo_out' --neg plot motif distributions in this set as well in the (positive sequences) --disc use Fisher's exact test instead of the binomial test to compare the control and the treatment (requires --neg ) --xalph Name of the file containing a custom alphabet, which specifies that motifs should be converted; --bfile background frequency model for PWMs; default: base frequencies in input sequences --local compute the enrichment of all regions; default: enrichment of central regions only --maxreg maximum width of any region to consider; default: use the sequence length --minreg minimum width of any region to consider; must be less than ; default: 1 bp --score score threshold for PWMs, in bits; sequences without a site with score >= are ignored; default: %.1g --optimize_score search for optimized score above the threshold given by '--score' argument. Slow computation due to multiple tests. default: use fixed score threshold --norc do not scan with the reverse complement motif --sep scan separately with reverse complement motif; (requires --norc) --flip 'flip' sequences so that matches on the reverse strand are 'reflected' around center; default: do not flip sequences --seqlen use sequences with this length; default: use sequences with the same length as the first --motif only scan with this motif; options may be repeated to specify more than one motif; default: scan with all motifs --motif-pseudo pseudo-count to use creating PWMs; default: %.3g --ethresh evalue threshold for including in results; default: %g --desc include the description in the output; default: no description --dfile use the file content as the description; default: no descriptionn --noseq do not store sequence IDs in HTML output; default: IDs are stored in the HTML output --verbosity [1|2|3|4] verbosity of output: 1 (quiet) - 4 (dump); default: %d --version print the version and exit failed to open sequence file `%s'failed to close sequence file Skipping sequence %s as its length (%d) does not match the expected length (%d). Failed to find a single sequence with the expected length %d counts->allocated == target->allocatedmm_resize(seq_sites->sites,seq_sites->allocated,SEQ_SITE_T) failed! rev_pssm == ((void *)0) || (((rev_pssm)->scale) == ((pssm)->scale) && ((rev_pssm)->offset) == ((pssm)->offset))## # Detailed descriptions of columns in this file: # # db: The name of the database (file name) that contains the motif. # id: A name for the motif that is unique in the motif database file. # alt: An alternate name of the motif that may be provided # in the motif database file. # consensus: A consensus sequence computed from the motif. # E-value: The expected number motifs that would have least one. # region as enriched for best matches to the motif as the reported region. # The E-value is the p-value multiplied by the number of motifs in the # input database(s). # adj_p-value: The probability that any tested region would be as enriched for # best matches to this motif as the reported region is. # By default the p-value is calculated by using the one-tailed binomial # test on the number of sequences with a match to the motif # that have their best match in the reported region, corrected for # the number of regions and score thresholds tested. # The test assumes that the probability that the best match in a sequence # falls in the region is the region width divided by the # number of places a motif # can align in the sequence (sequence length minus motif width plus 1). # When CentriMo is run in discriminative mode with a negative # set of sequences, the p-value of a region is calculated # using the Fisher exact test on the # enrichment of best matches in the positive sequences relative # to the negative sequences, corrected # for the number of regions and score thresholds tested. # The test assumes that the probability that the best match (if any) # falls into a given region # is the same for all positive and negative sequences. # log_adj_p-value: Log of adjusted p-value. # bin_location: Location of the center of the most enriched region. # bin_width: The width (in sequence positions) of the most enriched region. # A best match to the motif is counted as being in the region if the # center of the motif falls in the region. # total_width: The window maximal size which can be reached for this motif: # rounded(sequence length - motif length +1)/2 # sites_in_bin: The number of (positive) sequences whose best match to the motif # falls in the reported region. # Note: This number may be less than the number of # (positive) sequences that have a best match in the region. # The reason for this is that a sequence may have many matches that score # equally best. # If n matches have the best score in a sequence, 1/n is added to the # appropriate bin for each match. # total_sites: The number of sequences containing a match to the motif # above the score threshold. # p_success: The probability of falling in the enriched window: # bin width / total width # p-value: The uncorrected p-value before it gets adjusted to the # number of multiple tests to give the adjusted p-value. # mult_tests: This is the number of multiple tests (n) done for this motif. # It was used to correct the original p-value of a region for # multiple tests using the formula: # p' = 1 - (1-p)^n where p is the uncorrected p-value. # The number of multiple tests is the number of regions # considered times the number of score thresholds considered. # It depends on the motif length, sequence length, and the type of # optimizations being done (central enrichment, local enrichment, # score optimization). # neg_sites_in_bin: The number of negative sequences where the best # match to the motif falls in the reported region. # This value is rounded but the underlying value may contain # fractional counts. # Note: This number may be less than the number of negative have a # best match in the region. # The reason for this is that a sequence may have many matches that # score equally best. # If n matches have the best score in a sequence, 1/n is added to the # appropriate bin for each match. # neg_sites: The number of negative sequences containing a match to the # motif above the minimum score threshold. # When score optimization is enabled the score threshold may be raised # higher than the minimum. # neg_adj_pvalue: The probability that any tested region in the negative # sequences would be as enriched for best matches to this motif # according to the Binomial test. # log_neg_adj_pvalue: Log of negative adjusted p-value. # fisher_adj_pvalue: Fisher adjusted p-value before it gets adjusted to the # number of motifs in the input database(s). # Refers to the E-value definition using the discriminative mode. # log_fisher_adj_pvalue: Log of Fisher adjusted p-value. Sequences and motifs are both requiredYou must supply a FASTA file with the negative dataset (--neg ) when you use discriminative mode (--disc).You must supply a FASTA file with the negative dataset (--neg ) to calculate Matthews correlation coefficient (--mcc).You must specify --minreg smaller than --maxreg.The option --sep can not be used with an unstranded alphabet.Discarding motif %s in %s (not selected). Discarding motif %s in %s (non-unique ID). Warning: Motif file %s contains no motifs. Couldn't create output directory %s. # WARNING: this file is not sorted! # db id alt consensus E-value adj_p-value log_adj_p-value bin_location bin_width total_width sites_in_bin total_sites p_success p-value mult_tests neg_sites_in_bin neg_sites neg_adj_pvalue log_neg_adj_pvalue fisher_adj_pvalue log_fisher_adj_pvalueTemplate does not contain data section. Failed to open html template file. 166f68c0b08948c4f68a65de962954e476cde9b1Fri Apr 07 18:02:37 2017 -0700Using motif %s (%d/%d) of width %d. --maxreg (%d) too large for motif; setting to %d --minreg (%d) too large; setting to %d Warning: site counts don't sum to accurate value! %g != %ld Discarding redundant region (center: %d spread: %d) because it overlaps with a better region (center: %d spread: %d). %12.1f %9d %11d %12.0f %11ld %9.5f Found another JSON replacement! centrimo.coptions != ((void *)0)seq_sites != ((void *)0)undefinedcentrimo_out4.11.4 Unhandled option %dLoading sequences. Loading motifs. Expected %s alphabet motifs wcentrimo_data.js4.11.4versionrevisionreleaseCentriMoprogramcmdoptionsbfilemotif-pseudooptimize_scoreethreshminbinmaxbinlocalnorcsepnoseqneg_sequencesdiscmccjob_descriptionseqlenalphabetbackgroundskippednegative_sequence_dbmotif_dbsn_tests == n_actual_testsaltconsensusmotif_evaluemotif_nsitesn_testedscore_thresholdpwmneg_total_sitesneg_sitesseqspeakscenterspreadneg_log_adj_pvaluefisher_log_adj_pvalueDB %d MOTIF %s% 6.1f %g % 6.1f %g %g %4d %s %*s %s %.*fe%04.0f %15.2f %10d %12.0f %11ld %15.2f Program ends correctly xalphocmotifminregmaxregnoflipdescdfilenegverbositycentrimo.htmlcentrimo.txtsite_counts.txtcentrimo_template.htmlDDDDeD DDDDDD /D 4D D D DD)D8DDLDDDD Y@X@X@X@X@X@cX@Y@`Y@AY@4Y@Y@Y@Y@ W@W@W@W@W@jW@LW@?W@W@W@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@!Y@W@accumulate_site_countscalculate_best_windowsscore_sequence?$@@?$@@???+Uk@+@ !?Uk@?@iE>@~\>A~?@>@~)@@Qf@@ ta@&Ԏ@ ö)$@ ?@*hS@z2ގyE>[*7@ _ _Background file "%s" contained a symbol chain that was excessively long.Background file "%s" listed a symbol that is not in the visible ASCII range.Background file "%s" did not list a probability on the line listing the symbol chain "%s".Background file "%s" has a probability string that was excessively long for the symbol chain "%s".Background file "%s" has a probability string that could not be parsed as a probability for the symbol chain "%s".Background file "%s" has a probability of zero for the symbol chain "%s" which is not supported. Regenerate your background using pseudocounts to avoid this problem.Background file "%s" has junk text following the entry for the symbol chain "%s".Standard DNA alphabet should not produce warnings or errors!Standard RNA alphabet should not produce warnings or errors!Standard protein alphabet should not produce warnings or errors!Failed to open alphabet file: %s IO error reading alphabet file: %s WARNING: alphabet destroyed when the reference count was non-zero. %s%sncore > 0 && (alph)->complement[1] != 0)get_array_length(a1) >= alph->ncoreget_array_length(a2) >= alph->ncoreFailed to create DNA to protein translator!^[[:space:]]*([a-zA-Z])[[:space:]]+([+]?[0-9]*\.?[0-9]+([eE][-+]?[0-9]+)?)[[:space:]]*$ˑޑKjW&?OD>6 Ӽ?;v?&??Ț?_R?~t?M ɬ?i(2?/8Ut? 똗?t5?}]?}gt:ؤ?U?<(߲?3DZmc? @u?K?N?w?&k"> ?~Qr?E:?OO*,?,@? [ٲ?)kEѝ?_v?'_u?*J}?)+],?0|w?x[ȧ?KT5bf?&=F?yL|b?]Ȫ?=X?Qp>;າ?.KR?C}?wJ?f+/?\tz?_ ]?HЬ?d?pz?Ϣw*?2g?׃I?Lݤ?a[>?a? \k?>-z?FR?RU򱻠?complement_swap_freqsget_mast_frequenciesextrapolate_markov_modelresize_markov_modelalph_core_subsetalph_releasealph_hold\"\/\\ %06XDNAAdenineCytosineGuanineThymineWeakStrongAminoKetoPurinePyrimidineNot AAGTNot CACTNot GACGNot TACGTAny baseX.RNAUracilAUAGUACUNot UACGUProteinAlanineArginineAsparagineCysteineGlutamineGlycineHistidineLeucineLysineMethioninePhenylalanineProlineSerineThreonineTryptophanTyrosineValineAsparagine or Aspartic acidQEGlutamine or Glutamic acidLILeucine or IsoleucineARNDCEQGHILKMFPSTWYVAny amino acid*.wildcardalphabet.calphabet->references > 0ALPHABET RNA-LIKE DNA-LIKE PROTEIN-LIKE ~ %c = %s %c = %c %c = rnadnaprotein%s<%s name="%s" like="%s"%s n%cx%2X aliases="%s" complement="%c" equals="%s" colour="%06X"/> likesymbolssymbolaliasescolourcomplementequalssuper_i < 128asize0 > 0 && asize0 < asize1asize1 > asize0Alphabet uninitialized. Array unitialized. ABCDGHKMNRSTVWYABCDEFGHIKLMNPQRSTVWXYZindex >= 0nrdbTTTTTCTTATTGCTTCTCCTACTGATTATCATAATGGTTGTCGTAGTGTCTTCCTCATCGCCTCCCCCACCGACCACAGCTGCCGCGTATTACCATCACQCAACAGAATAACAAAAAGGATGACGAAGAGTGTTGCWTGGCGCCGACGGAGCAGAAGGGGTGGCGGAGGGXN š@@DB.?/ldG?i6w?:ƥ>mRzc?M>~?C?#u| >`toE>]s=>'n?P?Kَ2> 4>nP?ٶtA=>nv>>ػ>=Е?i&k? nk K?VI?mm_resize(new_array->items,num_items,ATYPE) failed! Error in extract_array. The staring position (%d) must be less than the current length of the array (%d). Error in extract_array. The end position (%d) must be less than or equal to the current length of the array (%d). Error in extract_array. The end position (%d) must be greater than the start position (%d). Attempted to retrieve minimum value from an empty array. Attempted to retrieve maximum value from an empty array. mm_resize(array->items,num_items,ATYPE) failed! Arrays have differing lengths (%d != %d). Error reading array at position %d. Unable to open file: %s. Error message: %s. Attempting to average the elements of an empty array. Computing correlation of vectors of different lengths.Invalid mixing parameter (%g). Error re-allocating array. %lf%*.*f Warning: variance of zero. array.creturn_value <= 1.0return_value >= -1.0total != 0.0normalize_subarraycorrelationXN B?arraylst_create_sized: size must be zero or larger. arraylst_preallocate: arraylst is null! arraylst_preallocate: size is smaller than zero. arraylst_fit: arraylst is null! arraylst_is_empty: arraylst is null! arraylst_size: arraylst is null! arraylst_put_n: arraylst is null! arraylst_put_n: index must be between zero and size inclusive. arraylst_put_n: times must be larger or equal to zero. arraylst_set: arraylst is NULL! arraylst_set: index must be within bounds. arraylst_set: index1 must be within bounds. arraylst_set: index2 must be within bounds. arraylst_get: arraylst is NULL! arraylst_get: index must be within bounds. arraylst_map_range: arraylst is NULL! arraylst_map_range: map_fun is NULL! arraylst_map_range: count must be zero or more elements. arraylst_map_range: index must be within bounds. arraylst_map_range: index + count is larger than size! arraylst_map: arraylst is NULL! arraylst_map: map_fun is NULL! arraylst_map_range: fun is NULL! arraylst_remove_range: arraylst is NULL! arraylst_remove_range: count must be one or more elements. arraylst_remove_range: index must be within bounds. arraylst_remove_range: index + count is larger than size! arraylst_clear: arraylst is NULL! arraylst_take: No more items to take from arraylst! arraylst_apply: arraylst is NULL! arraylst_destroy: arraylst is null! arraylst_accumulate_range: arraylst is NULL! arraylst_accumulate_range: accumulator_fun is NULL! arraylst_accumulate_range: count must be zero or more elements. arraylst_accumulate_range: index must be within bounds. arraylst_accumulate_range: index + count is larger than size! arraylst_accumulate: arraylst is NULL! arraylst_accumulate: accumulator_fun is NULL! arraylst_apply: fun is NULL! a (%g) or b (%g) too big, or MAXIT (%d) too small in betacf. Input x is %g. Returning %g. Bad x in routine betaiu<7~Ynv !>Error reading sequence ID. fasta-io.cin sequence %s. >%s %s %.*s %s Couldn't open the file %s. FASTA sequences(int)strlen(raw_sequence) < max_charsWarning: Skipping character %c in sequence %s. Warning: Converting illegal character %c to %c Sequence %s is too long (maximum=%d). Read sequence %s of length %d. get_seq_length(*sequence) < max_charsFailed to read a single sequence from the given FASTA file. Sequence %s:%d-? is too long (maximum=%d). Error while reading %s as a FASTA file. read_one_fasta_segmentread_raw_sequencesource nameSource file already closed. Destination file not set. ; %sError reading source Impossible statehtml-monolith.cimage/pngdata:%s;base64,Bad file name. [a-zA-Z_-]+\.(js|css|png)$