📄 fasts3.1
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.TH FASTS/TFASTSv3 1 local.SH NAMEfasts3, fasts3_t \- compare several short peptide sequences against a proteindatabase using a modified fasta algorithm.tfasts3, tfasts3_t \- compare short pepides against atranslated DNA database..SH DESCRIPTION.B fasts3and.B tfasts3are designed to compare set of (presumably non-contiguous) peptides toa protein (fasts3) or translated DNA (tfasts3) database.fasts3/tfasts3 are designed particularly for short peptide data frommass-spec analysis of protein digests. Unlike the traditional.B fasta3search, which uses a protein or DNA sequence,.B fasts3and.B tfasts3work with a query sequence of the form:.in +5.nf>tests from mgstm1MLLE,MILGYW,MGADP,MLCYNP.fi.in 0This sequence indicates that four peptides are to be used. When thissequence is compared against mgstm1.aa (included with thedistribution), the result is:.nf.ft C.in +5testf MILGYW----------MLLE------------MGDAP----------- :::::: :::: ::::: GT8.7 MPMILGYWNVRGLTHPIRMLLEYTDSSYDEKRYTMGDAPDFDRSQWLNEK 10 20 30 40 50testf -------------------------------------------------- GT8.7 FKLGLDFPNLPYLIDGSHKITQSNAILRYLARKHHLDGETEEERIRADIV 60 70 80 90 100 20 testf ------------MLCYNP ::::::GT8.7 ENQVMDTRMQLIMLCYNPDFEKQKPEFLKTIPEKMKLYSEFLGKRPWFAG 110 120 130 140 150.in 0.ft P.fi.SH Options.LP.B fasts3and.B tfasts3can accept a query sequence from the unix "stdin" data stream. This makes it mucheasier to use fasta3 and its relatives as part of a WWW page. Toindicate that stdin is to be used, use "-" or "@" as the querysequence file name..TP\-b #number of best scores to show (must be < -E cutoff).TP\-d #number of best alignments to show ( must be < -E cutoff).TP\-Dturn on debugging mode. Enables checks on sequence alphabet thatcause problems with tfastx3, tfasty3, tfasta3..TP\-E #Expectation value limit for displaying scores andalignments. Expectation values for.B fasts3and.B tfasts3are not as accurate as those for the other .B fasta3programs..TP\-Hturn off histogram display.TP\-icompare against only the reverse complement of the library sequence..TP\-Lreport long sequence description in alignments.TP\-m 0,1,2,3,4,5,6,9,10alignment display options.TP\-N #break long library sequences into blocks of # residues. Useful forbacterial genomes, which have only one sequence entry. -N 2000 workswell for well for bacterial genomes..TP\-O filesend output to file.TP\-q/-Qquiet option; do not prompt for input.TP \-R filesave all scores to statistics file.TP\-S #offset substitution matrix values by a constant #.TP\-s namespecify substitution matrix. BLOSUM50 is used by default;PAM250, PAM120, and BLOSUM62 can be specified by setting -s P120,P250, or BL62. With this version, many more scoring matrices areavailable, including BLOSUM80 (BL80), and MDM_10, MDM_20, MDM_40 (M10,M20, M40). Alternatively, BLASTP1.4 format scoring matrix files can bespecified..TP\-T #(threaded, parallel only) number of threads or workers to use (set bydefault to 4 at compile time)..TP\-t #Translation table - tfasts3 can use the BLAST tranlation tables. See\fChttp://www.ncbi.nlm.nih.gov/htbin-post/Taxonomy/wprintgc?mode=c/\fP..TP\-w #line width for similarity score, sequence alignment, output..TP\-x "#,#"offsets query, library sequence for numbering alignments.TP\-z #Specify statistical calculation. Default is -z 1, which usesregression against the length of the library sequence. -z 0 disablesstatistics. -z 2 uses the ln() length correction. -z 3 uses Altschuland Gish's statistical estimates for specific protein BLOSUM scoringmatrices and gap penalties. -z 4: an alternate regression method..TP\-Z db_sizeSet the apparent database size used for expectation value calculations..TP\-3(TFASTS3 only) use only forward frame translations.SH Environment variables:.TPFASTLIBSlocation of library choice file (-l FASTLIBS).TPSMATRIXdefault scoring matrix (-s SMATRIX).TPSRCH_URLthe format string used to define the option to re-search thedatabase..TPREF_URLthe format string used to define the option to lookup the librarysequence in entrez, or some other database..SH AUTHORBill Pearson.brwrp@virginia.EDU
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