• DNA sequence open reading frames (ORFs) | DNA序列的开放阅读框ORF预测


    常见的ORF预测工具

    Open Reading Frame Finder - NCBI

    ORF Finder - SMS

    OrfPredictor  - YSU

    基本概念

    开放阅读框(英语:Open reading frame;缩写:ORF;其他译名:开放阅读框架、开放读架等)是指在给定的阅读框架中,不包含终止密码子的一串序列。这段序列是生物个体的基因组中,可能作为蛋白质编码序列的部分。基因中的ORF包含并位于开始编码与终止编码之间。由于一段DNA或RNA序列有多种不同读取方式,因此可能同时存在许多不同的开放阅读框架。有一些计算机程序可分析出最可能是蛋白质编码的序列。

    关键词:

    1. 不包含终止密码子的一串序列;

    2. 可能作为蛋白质编码序列的部分;

    3. 有多种不同读取方式,因此可能同时存在许多不同的开放阅读框架;

    4. 有些工具会用blast比对来提高可信度

    示例

    一段5'-UCUAAAGGUCCA-3'序列。此序列共有3种读取法:

    1. UCU AAA GGU CCA
    2. CUA AAG GUC
    3. UAA AGG UCC

    由于UAA为终止编码,因此第三种读取法不具编译出蛋白质的潜力,故只有前两者为开放阅读框架

    个人当然是推荐使用NCBI大佬开发的工具的啦,发文章可信度高些。

    以下是Linux版该工具的说明:

    USAGE
      ORFfinder [-h] [-help] [-xmlhelp] [-in Input_File] [-id Accession_GI]
        [-b begin] [-e end] [-c circular] [-g Genetic_code] [-s Start_codon]
        [-ml minimal_length] [-n nested_ORFs] [-strand Strand] [-out Output_File]
        [-outfmt output_format] [-logfile File_Name] [-conffile File_Name]
        [-version] [-version-full] [-dryrun]
    
    DESCRIPTION
       Searching open reading frames in a sequence
    
    OPTIONAL ARGUMENTS
     -h
       Print USAGE and DESCRIPTION;  ignore all other parameters
     -help
       Print USAGE, DESCRIPTION and ARGUMENTS; ignore all other parameters
     -xmlhelp
       Print USAGE, DESCRIPTION and ARGUMENTS in XML format; ignore all other
       parameters
     -logfile <File_Out>
       File to which the program log should be redirected
     -conffile <File_In>
       Program's configuration (registry) data file
     -version
       Print version number;  ignore other arguments
     -version-full
       Print extended version data;  ignore other arguments
     -dryrun
       Dry run the application: do nothing, only test all preconditions
    
     *** Input query options (one of them has to be provided):
     -in <File_In>
       name of file with the nucleotide sequence in FASTA format
       (more than one sequence is allowed)
       Default = `'
     -id <String>
       Accession or gi number of the nucleotide sequence
       (ignored, if the file name is provided)
       Default = `'
    
     *** Query sequence details:
     -b <Integer>
       Start address of sequence fragment to be processed
       Default = `1'
     -e <Integer>
       Stop address of sequence fragment to be processed (0 - to the end of the
       sequence)
       Default = `0'
     -c <Boolean>
       Is the sequence circular? (t/f) *** Under development
       Default = `false'
    
     *** Search parameters:
     -g <Integer>
       Genetic code to use (1-31)
       see https://www.ncbi.nlm.nih.gov/Taxonomy/Utils/wprintgc.cgi for details
       Default = `1'
     -s <Integer>
       ORF start codon to use:
           0 = "ATG" only
           1 = "ATG" and alternative initiation codons
           2 = any sense codon
       Default = `1'
     -ml <Integer>
       Minimal length of the ORF (nt)
       Value less than 30 is automatically changed by 30.
       Default = `75'
     -n <Boolean>
       Ignore nested ORFs (completely placed within another)
       Default = `false'
     -strand <String>
       Output ORFs on specified strand only (both|plus|minus)
       Default = `both'
    
     *** Output options:
     -out <File_Out>
       Output file name
     -outfmt <Integer>
       Output options:
           0 = list of ORFs in FASTA format
           1 = CDS in FASTA format
           2 = Text ASN.1
           3 = Feature table
       Default = `0'
    

      

    ORFfinder -in in.fasta -s 2 -ml 100 -out test.out -outfmt 3
    

      

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  • 原文地址:https://www.cnblogs.com/leezx/p/8645696.html
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