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📄 est2genome.ihelp

📁 emboss的linux版本的源代码
💻 IHELP
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   Standard (Mandatory) qualifiers:  [-estsequence]       seqall     Spliced EST nucleotide sequence(s)  [-genomesequence]    sequence   Unspliced genomic nucleotide sequence  [-outfile]           outfile    [*.est2genome] Output file name   Additional (Optional) qualifiers:   -match              integer    [1] Score for matching two bases (Any                                  integer value)   -mismatch           integer    [1] Cost for mismatching two bases (Any                                  integer value)   -gappenalty         integer    [2] Cost for deleting a single base in                                  either sequence, excluding introns (Any                                  integer value)   -intronpenalty      integer    [40] Cost for an intron, independent of                                  length. (Any integer value)   -splicepenalty      integer    [20] Cost for an intron, independent of                                  length and starting/ending on donor-acceptor                                  sites (Any integer value)   -minscore           integer    [30] Exclude alignments with scores below                                  this threshold score. (Any integer value)   Advanced (Unprompted) qualifiers:   -reverse            boolean    Reverse the orientation of the EST sequence   -[no]splice         boolean    [Y] Use donor and acceptor splice sites. If                                  you want to ignore donor-acceptor sites then                                  set this to be false.   -mode               menu       [both] This determines the comparion mode.                                  The default value is 'both', in which case                                  both strands of the est are compared                                  assuming a forward gene direction (ie GT/AG                                  splice sites), and the best comparsion                                  redone assuming a reversed (CT/AC) gene                                  splicing direction. The other allowed modes                                  are 'forward', when just the forward strand                                  is searched, and 'reverse', ditto for the                                  reverse strand. (Values: both (Both                                  strands); forward (Forward strand only);                                  reverse (Reverse strand only))   -[no]best           boolean    [Y] You can print out all comparisons                                  instead of just the best one by setting this                                  to be false.   -space              float      [10.0] For linear-space recursion. If                                  product of sequence lengths divided by 4                                  exceeds this then a divide-and-conquer                                  strategy is used to control the memory                                  requirements. In this way very long                                  sequences can be aligned.                                  If you have a machine with plenty of memory                                  you can raise this parameter (but do not                                  exceed the machine's physical RAM) (Any                                  numeric value)   -shuffle            integer    [0] Shuffle (Any integer value)   -seed               integer    [20825] Random number seed (Any integer                                  value)   -align              boolean    Show the alignment. The alignment includes                                  the first and last 5 bases of each intron,                                  together with the intron width. The                                  direction of splicing is indicated by angle                                  brackets (forward or reverse) or ????                                  (unknown).   -width              integer    [50] Alignment width (Any integer value)   Associated qualifiers:   "-estsequence" 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   "-genomesequence" associated qualifiers   -sbegin2            integer    Start of the sequence to be used   -send2              integer    End of the sequence to be used   -sreverse2          boolean    Reverse (if DNA)   -sask2              boolean    Ask for begin/end/reverse   -snucleotide2       boolean    Sequence is nucleotide   -sprotein2          boolean    Sequence is protein   -slower2            boolean    Make lower case   -supper2            boolean    Make upper case   -sformat2           string     Input sequence format   -sdbname2           string     Database name   -sid2               string     Entryname   -ufo2               string     UFO features   -fformat2           string     Features format   -fopenfile2         string     Features file name   "-outfile" associated qualifiers   -odirectory3        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 messages

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