⭐ 欢迎来到虫虫下载站! | 📦 资源下载 📁 资源专辑 ℹ️ 关于我们
⭐ 虫虫下载站

📄 trimest.ihelp

📁 emboss的linux版本的源代码
💻 IHELP
字号:
   Standard (Mandatory) qualifiers:  [-sequence]          seqall     Nucleotide sequence(s) filename and optional                                  format, or reference (input USA)  [-outseq]            seqoutall  [<sequence>.<format>] Sequence set(s)                                  filename and optional format (output USA)   Additional (Optional) qualifiers:   -minlength          integer    [4] This is the minimum length that a poly-A                                  (or poly-T) tail must have before it is                                  removed. If there are mismatches in the tail                                  than there must be at least this length of                                  poly-A tail before the mismatch for the                                  mismatch to be considered part of the tail.                                  (Integer 1 or more)   -mismatches         integer    [1] If there are this number or fewer                                  contiguous non-A bases in a poly-A tail                                  then, if there are '-minlength' 'A' bases                                  before them, they will be considered part of                                  the tail and removed .                                  For example the terminal 4 A's of GCAGAAAA                                  would be removed with the default values of                                  -minlength=4 and -mismatches=1 (There are                                  not at least 4 A's before the last 'G' and                                  so only the A's after it are considered to                                  be part of the tail). The terminal 9 bases                                  of GCAAAAGAAAA would be removed; There are                                  at least -minlength A's preceeding the last                                  'G', so it is part of the tail. (Integer 0                                  or more)   -[no]reverse        boolean    [Y] When a poly-T region at the 5' end of                                  the sequence is found and removed, it is                                  likely that the sequence is in the reverse                                  sense. This option will change the sequence                                  to the forward sense when it is written out.                                  If this option is not set, then the sense                                  will not be changed.   -tolower            toggle     [N] The poly-A region can be 'masked' by                                  converting the sequence characters to                                  lower-case. Some non-EMBOSS programs e.g.                                  fasta can interpret this as a masked region.                                  The sequence is unchanged apart from the                                  case change. You might like to ensure that                                  the whole sequence is in upper-case before                                  masking the specified regions to lower-case                                  by using the '-supper' sequence qualifier.   Advanced (Unprompted) qualifiers:   -[no]fiveprime      boolean    [Y] If this is set true, then the 5' end of                                  teh sequence is inspected for poly-T tails.                                  These will be removed if they are longer                                  than any 3' poly-A tails. If this is false,                                  then the 5' end is ignored.   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   "-outseq" associated qualifiers   -osformat2          string     Output seq format   -osextension2       string     File name extension   -osname2            string     Base file name   -osdirectory2       string     Output directory   -osdbname2          string     Database name to add   -ossingle2          boolean    Separate file for each entry   -oufo2              string     UFO features   -offormat2          string     Features format   -ofname2            string     Features file name   -ofdirectory2       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

⌨️ 快捷键说明

复制代码 Ctrl + C
搜索代码 Ctrl + F
全屏模式 F11
切换主题 Ctrl + Shift + D
显示快捷键 ?
增大字号 Ctrl + =
减小字号 Ctrl + -