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📄 einverted.txt

📁 emboss的linux版本的源代码
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                                 einverted Function   Finds DNA inverted repeatsDescription   einverted looks for inverted repeats (stem loops) in a nucleotide   sequence.   It will find inverted repeats that include a proprtion of mismatches   and gaps (bulges in the stem loop).Algorithm   It works by finding alignments between the sequence and its reverse   complement that exceed a threshold score. Gaps and Mismatches are   assigned a penalty (negative) score. Matches are assigned a positive   score. The score is calculated by summing the values of each match,   the penalties of each mismatch and the large penalties of any gaps.   Any region whose score exceeds the threshold is reported.   einverted uses dynamic programming and thus is guaranteed to find the   optimal alignment, but is slower than, for example, a self-by-self   BLAST. It can find multiple inverted repeats in a sequence.   einverted does not report overlapping matches.   The original "inverted" program was written to annotate the nematode   genome. Excluding overlapping repeats saved problems with simple   repeat sequences in this genome.Usage   Here is a sample session with einverted% einverted tembl:hsts1 Finds DNA inverted repeatsGap penalty [12]: Minimum score threshold [50]: Match score [3]: Mismatch score [-4]: Sanger Centre program inverted output file [hsts1.inv]: File for sequence of regions of inverted repeats. [hsts1.fasta]:    Go to the input files for this example   Go to the output files for this exampleCommand line arguments   Standard (Mandatory) qualifiers:  [-sequence]          seqall     Nucleotide sequence(s) filename and optional                                  format, or reference (input USA)   -gap                integer    [12] Gap penalty (Any integer value)   -threshold          integer    [50] Minimum score threshold (Any integer                                  value)   -match              integer    [3] Match score (Any integer value)   -mismatch           integer    [-4] Mismatch score (Any integer value)  [-outfile]           outfile    [*.einverted] Sanger Centre program inverted                                  output file  [-outseq]            seqout     [.] The sequence of the                                  inverted repeat regions without gap                                  characters.   Additional (Optional) qualifiers:   -maxrepeat          integer    [2000] Maximum separation between the start                                  of repeat and the end of the inverted repeat                                  (the default is 2000 bases). (Any integer                                  value)   Advanced (Unprompted) qualifiers: (none)   Associated qualifiers:   "-sequence" associated qualifiers   -sbegin1            integer    Start of each sequence to be used   -send1              integer    End of each sequence to be used   -sreverse1          boolean    Reverse (if DNA)   -sask1              boolean    Ask for begin/end/reverse   -snucleotide1       boolean    Sequence is nucleotide   -sprotein1          boolean    Sequence is protein   -slower1            boolean    Make lower case   -supper1            boolean    Make upper case   -sformat1           string     Input sequence format   -sdbname1           string     Database name   -sid1               string     Entryname   -ufo1               string     UFO features   -fformat1           string     Features format   -fopenfile1         string     Features file name   "-outfile" associated qualifiers   -odirectory2        string     Output directory   "-outseq" associated qualifiers   -osformat3          string     Output seq format   -osextension3       string     File name extension   -osname3            string     Base file name   -osdirectory3       string     Output directory   -osdbname3          string     Database name to add   -ossingle3          boolean    Separate file for each entry   -oufo3              string     UFO features   -offormat3          string     Features format   -ofname3            string     Features file name   -ofdirectory3       string     Output directory   General qualifiers:   -auto               boolean    Turn off prompts   -stdout             boolean    Write standard output   -filter             boolean    Read standard input, write standard output   -options            boolean    Prompt for standard and additional values   -debug              boolean    Write debug output to program.dbg   -verbose            boolean    Report some/full command line options   -help               boolean    Report command line options. More                                  information on associated and general                                  qualifiers can be found with -help -verbose   -warning            boolean    Report warnings   -error              boolean    Report errors   -fatal              boolean    Report fatal errors   -die                boolean    Report dying program messagesInput file format   The input for einverted is a nucleotide sequence  Input files for usage example   'tembl:hsts1' is a sequence entry in the example nucleic acid database   'tembl'  Database entry: tembl:hsts1ID   HSTS1      standard; DNA; HUM; 18596 BP.XXAC   D00596;XXSV   D00596.1XXDT   17-JUL-1991 (Rel. 28, Created)DT   27-OCT-1998 (Rel. 57, Last updated, Version 2)XXDE   Homo sapiens gene for thymidylate synthase, exons 1, 2, 3, 4, 5, 6, 7,DE   complete cds.XXKW   thymidylate syntase.XXOS   Homo sapiens (human)OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;OC   Eutheria; Primates; Catarrhini; Hominidae; Homo.XXRN   [1]RP   1-18596RX   MEDLINE; 91056070.RA   Kaneda S., Nalbantoglu J., Takeishi K., Shimizu K., Gotoh O., Seno T.,RA   Ayusawa D.;RT   "Structural and Functional Analysis of the Human Thymidylate SynthaseRT   Gene";RL   J. Biol. Chem. 265:20277-20284(1990).XXDR   SWISS-PROT; P04818; TYSY_HUMAN.XXCC   These data kindly submitted in computer readable form by:CC   Sumiko KanedaCC   National Institute of GeneticsCC   1111 YataCC   Mishima 411CC   JapanCC   Phone:  +81-559-72-2732CC   Fax:    +81-559-71-3651XXFH   Key             Location/QualifiersFHFT   source          1..18596FT                   /chromosome="18"FT                   /db_xref="taxon:9606"FT                   /sequenced_mol="DNA"FT                   /organism="Homo sapiens"FT                   /clone="lambdaHTS-1 and lambdaHTS-3"FT                   /map="18p11.32"FT   repeat_unit     1..148FT                   /note="Alu sequence"FT   repeat_unit     202..477  [Part of this file has been deleted for brevity]     ttttgttttt agcttcagcg agaacccaga cctttcccaa agctcaggat tcttcgaaaa     15660     gttgagaaaa ttgatgactt caaagctgaa gactttcaga ttgaagggta caatccgcat     15720     ccaactatta aaatggaaat ggctgtttag ggtgctttca aaggagctcg aaggatattg     15780     tcagtcttta ggggttgggc tggatgccga ggtaaaagtt ctttttgctc taaaagaaaa     15840     aggaactagg tcaaaaatct gtccgtgacc tatcagttat taatttttaa ggatgttgcc     15900     actggcaaat gtaactgtgc cagttctttc cataataaaa ggctttgagt taactcactg     15960     agggtatctg acaatgctga ggttatgaac aaagtgagga gaatgaaatg tatgtgctct     16020     tagcaaaaac atgtatgtgc atttcaatcc cacgtactta taaagaaggt tggtgaattt     16080     cacaagctat ttttggaata tttttagaat attttaagaa tttcacaagc tattccctca     16140     aatctgaggg agctgagtaa caccatcgat catgatgtag agtgtggtta tgaactttaa     16200     agttatagtt gttttatatg ttgctataat aaagaagtgt tctgcattcg tccacgcttt     16260     gttcattctg tactgccact tatctgctca gttccttcct aaaatagatt aaagaactct     16320     ccttaagtaa acatgtgctg tattctggtt tggatgctac ttaaaagagt atattttaga     16380     aataatagtg aatatatttt gccctatttt tctcatttta actgcatctt atcctcaaaa     16440     tataatgacc atttaggata gagttttttt tttttttttt taaactttta taaccttaaa     16500     gggttatttt aaaataatct atggactacc attttgccct cattagcttc agcatggtgt     16560     gacttctcta ataatatgct tagattaagc aaggaaaaga tgcaaaacca cttcggggtt     16620     aatcagtgaa atatttttcc cttcgttgca taccagatac ccccggtgtt gcacgactat     16680     ttttattctg ctaatttatg acaagtgtta aacagaacaa ggaattattc caacaagtta     1674

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