时间戳

首页 > 解决方案 > 使用坐标（基​​因）文件的脚本

python - 使用坐标（基​​因）文件的脚本

问题描述

我有一个变体表（variation.txt），它是一个非常大的文件。染色体编号的第一列和第二列是变异的位置。我有第二个文件annotation.txt，其中包含 37,000 个基因（第 1 列）、它们的染色体编号（第 2 列）、它们的开始和结束坐标（第 3 列）的列表，然后是一些细节

我必须将变异（基于染色体编号及其位置）分配给基因。首先，它应该在两个文件中寻找匹配的染色体编号，如果匹配，变异的坐标应该在（包括）基因的开始和结束位置。我曾在 python 中尝试过，但需要很长时间。此外，我想要修改后的输出，如下所示。基因可以具有重叠的坐标，并且给定的变异可以是多个重叠基因的一部分。请帮忙。

变异.txt

SL3.0ch02   702679  C   A   -   -   -   -   -   -   -   -
SL3.0ch01   711131  A   G   -   -   -   -   -   -   -   -
SL3.0ch00   715124  G   A   -   -   -   -   -   -   -   -
SL3.0ch00   719289  C   T   -   -   -   -   -   -   -   -
SL3.0ch00   720926  A   C   -   -   -   -   -   -   -   -
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS     NONSYNONYMOUS   W/G     52  0   novel   DELETERIOUS (*WARNING! Low confidence)
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS     SYNONYMOUS  G/G     49  1   novel   TOLERATED
SL3.0ch00   723903  T   C   Solyc00g005060.1    CDS     SYNONYMOUS  G/G     37  1   novel   TOLERATED

注释.txt

Solyc00g005000.3.1  SL3.0ch02   702600  702900  +   Eukaryotic aspartyl protease family protein
Solyc00g005040.3.1  SL3.0ch01   715100  715200  +   Potassium channel
Solyc00g005050.3.1  SL3.0ch00   715150  715300  -   UPF0664 stress-induced protein C29B12.11c
Solyc00g005060.1.1  SL3.0ch00   723741  724013  -   LOW QUALITY:Cyclin/Brf1-like TBP-binding protein
Solyc00g005080.2.1  SL3.0ch00   723800  723900  -   LOW QUALITY:Protein Ycf2
Solyc00g005084.1.1  SL3.0ch05   809593  813633  +   UDP-Glycosyltransferase superfamily protein
Solyc00g005090.1.1  SL3.0ch07   1061632 1061916 -   LOW QUALITY:DYNAMIN-like 1B
Solyc00g005092.1.1  SL3.0ch01   1127794 1144385 +   Serine/threonine phosphatase-like protein
Solyc00g005094.1.1  SL3.0ch00   1144958 1146952 -   Glucose-6-phosphate 1-dehydrogenase 3, chloroplastic
Solyc00g005096.1.1  SL3.0ch00   1734562 1736567 +   RWP-RK domain-containing protein

期望的输出：

SL3.0ch02   702679  C   A   -   -   -   -   -   -   -   -   Solyc00g005000.3.1  
SL3.0ch00   715124  G   A   -   -   -   -   -   -   -   -   Solyc00g005040.3.1  
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS NONSYNONYMOUS   W/G 52  0   novel   DELETERIOUS (*WARNING! Low confidence)  Solyc00g005060.1.1  
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS NONSYNONYMOUS   W/G 52  0   novel   DELETERIOUS (*WARNING! Low confidence)  Solyc00g005080.2.1  
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS SYNONYMOUS  G/G 49  1   novel   TOLERATED   Solyc00g005060.1.1  
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS SYNONYMOUS  G/G 49  1   novel   TOLERATED   Solyc00g005080.2.1  
SL3.0ch00   723903  T   C   Solyc00g005060.1    CDS SYNONYMOUS  G/G 37  1   novel   TOLERATED   Solyc00g005060.1.1

代码：

import re
file1 = open("variation", "r")
file2 = open("annotation.txt", "r")
probe_id = file1.read().splitlines()
loc_id = file2.read().splitlines()

for i in probe_id:
    i=i.rstrip()
    probe_info=i.split('\t')
    probe_info[1]=probe_info[1].strip()
    probe_info[0]=probe_info[0].strip()
    #print probe_info[1]
    gene_list=[]
    for j in loc_id:
        loc_info=j.split('\t')
        loc_info[2]=loc_info[2].strip()
        loc_info[3]=loc_info[3].strip()
        if loc_info[1]==probe_info[0]:
            if (int(probe_info[1]) >= int(loc_info[2])):
                 if (int(probe_info[1]) <=int(loc_info[3])):
                    gene_list.append(loc_info[0])
    if len(gene_list)!=0:
        print i+"\t"+str(gene_list)

电流输出：

SL3.0ch02   702679  C   A   -   -   -   -   -   -   -   -   ['Solyc00g005000.3.1']  
SL3.0ch00   715124  G   A   -   -   -   -   -   -   -   -   ['Solyc00g005040.3.1']  
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS NONSYNONYMOUS   W/G 52  0   novel   DELETERIOUS (*WARNING! Low confidence)  ['Solyc00g005060.1.1', 'Solyc00g005080.2.1']    
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS SYNONYMOUS  G/G 49  1   novel   TOLERATED   ['Solyc00g005060.1.1', 'Solyc00g005080.2.1']    
SL3.0ch00   723903  T   C   Solyc00g005060.1    CDS SYNONYMOUS  G/G 37  1   novel   TOLERATED   ['Solyc00g005060.1.1']

标签： pythonbashawk

解决方案

这是 GNU awk 的开始，它匹配染色体编号和范围内的位置：

$ awk '
NR==FNR {
    a[$2][$3 " " $4]=$0                     # store the annotations
    next
}
($1 in a){                                  # if chromosome found
    for(i in a[$1])                         # process all the ranges
        if(split(i,t)&&$2>=t[1]&&$2<=t[2])  # if there is a match
            print                           # output
}' anno vari

输出大气压：

SL3.0ch02   702679  C   A   -   -   -   -   -   -   -   -
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS     NONSYNONYMOUS   W/G     52  0   novel   DELETERIOUS (*WARNING! Low confidence)
SL3.0ch00   723860  A   C   Solyc00g005060.1    CDS     NONSYNONYMOUS   W/G     52  0   novel   DELETERIOUS (*WARNING! Low confidence)
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS     SYNONYMOUS  G/G     49  1   novel   TOLERATED
SL3.0ch00   723867  A   C   Solyc00g005060.1    CDS     SYNONYMOUS  G/G     49  1   novel   TOLERATED
SL3.0ch00   723903  T   C   Solyc00g005060.1    CDS     SYNONYMOUS  G/G     37  1   novel   TOLERATED

推荐阅读