脚本一起工作协调(基因)文件

问题描述 投票:0回答:2

我有一个变化表(variation.txt),这是一个非常大的文件。在染色体数目和第二列中的第一列是变化的位置。我有有37,000个基因的列表(第1列),它们的染色体数目(第2列),他们的起点和终点坐标(第3列),第二个文件annotation.txt,其次是一些细节

我必须分配的变化(基于染色体数目和其位置)的基因。首先,它应该在这两个文件中匹配的染色体数目,如果匹配,该变化的坐标应为内(含)开始,该基因的末端位置。我曾在蟒蛇尝试,但它需要很长时间。此外,我想有一个修改的输出,如下所示。基因可以具有重叠的坐标和给定的变化可以是多种重叠基因的一部分。请帮助。

variation.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

annotation.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

所需的输出:

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  

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']  
python bash awk
2个回答
2
投票

这是GNU AWK相匹配的染色体数目和范围内的位置开始:

$ 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ATM:

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

2
投票

这将是有效的前处理“annotation.txt”,并创建一个字典提前,以减少循环计算。 请尝试以下方法:

#!/usr/bin/python

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

for i in loc_id:
    loc_info=i.split('\t')
    gene = loc_info[0].strip()
    chromosome = loc_info[1].strip()
    start = int(loc_info[2].strip())
    end = int(loc_info[3].strip())
    if (chromosome in annotation.keys()):
        annotation[chromosome].append([start, end, gene])
    else:
        annotation[chromosome] = [[start, end, gene]]

for i in probe_id:
    i = i.rstrip()
    probe_info = i.split('\t')
    position = int(probe_info[1].strip())
    chromosome = probe_info[0].strip()

    if (chromosome in annotation.keys()):
        for j in annotation[chromosome]:
            if (j[0] <= position and position <= j[1]):
                print i + '\t' + j[2]

输出:

SL3.0ch02   702679  C       A       -       -       -       -       -       -       -       -       Solyc00g005000.3.1
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

我想,该算法主要是接近@詹姆斯布朗的回答。 希望这可以帮助。

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