用python合并RepeatMasker预测结果中染色体的overlap区域

前言

RepeatMasker是一个通过已有数据库预测重复序列的软件,可以筛选DNA序列中的散在重复序列和低复杂序列,是重复序列注释的重要软件。

问题

我们想对RepeatMasker预测的结果文件进行重复序列的合并,也就是去除染色体之间的overlap区域同时将基因间距小于50个bp的也同样视为overlap,我们应该如何用python处理并生成新的预测结果?

思路

  1. 首先需要对文件进行预处理提取出需要处理的列,'//'可以忽略
  2. 对相同染色体序列按照升序进行归并排序
  3. 分别取相应染色体按照滑动窗口的思路进行双指针比对,注意gap=50

思路清晰,开始

1. 预处理

我们这里只需要结果文件的前三列,可以使用awk命令获取

awk '{for(i = 1; i <= 3; i++) printf("%s ", $i); printf("\n")}' result.txt >  pretreatment.txt  #result.txt为结果文件,pretreatment.txt为预处理结果文件

2. 将pretreatment.txt作为输入文件,

with open ('pretreatment.txt','r')as f:
    for i in f.readlines():
        if i.strip() == '//':
            continue
        c = i.strip().split('\t')
        b.append(c[0])
        a.append((c[0],int(c[1]),int(c[2])))
print ("全部染色体数量: "+str(len(a)))

3.去重+归并排序

c = [i for i in b_set if b.count(i) == 1]

for i in a:
    if i[0] not in c:
        continue
    a.remove(i)
    result.append((i[0],int(i[1]),int(i[2])))
print ("去重后染色体数量: "+str(len(a)))
a.sort(key = lambda x : (x[0], x[1], x[2])) #按照第一列,第二列,第三列分别排降升序

4.开始比对,gap=50

q = ''
start = 0
end = 0
tem1 = []
tem2 = []
gap = 50 

for i in a:
    if i[0] != q:
        if tem1:

            if tem1 not in tem2:
                tem2.append(tem1)
                tem1 = []

        q = I[0]
        start = int(i[1])
        end = int(i[2])
        continue

    if int(i[1]) < end or int(i[1]) - end < gap:
        if int(i[2]) > end:
            end = int(i[2])
            continue
        else:
            continue

    tem1.append([q,start,end])
    start = int(i[1])
    end = int(i[2])

5.将new_result.txt作为输出文件,生成结果

with open ('new_result.txt','w')as f:

    for i in tem2:
        for o in I:
            print (o[0],o[1],o[2],file=f)

    for i in result:
        print (i[0],i[1],i[2],file=f)

6. 完整代码

a = []
b = []

with open ('pretreatment.txt','r')as f:
    for i in f.readlines():
        if i.strip() == '//':
            continue
        c = i.strip().split('\t')
        b.append(c[0])
        a.append((c[0],int(c[1]),int(c[2])))
print ("全部染色体数量: "+str(len(a)))

b_set = set(b)

result = []

c = [i for i in b_set if b.count(i) == 1]

for i in a:
    if i[0] not in c:
        continue
    a.remove(i)
    result.append((i[0],int(i[1]),int(i[2])))

print ("去重后染色体数量: "+str(len(a)))

a.sort(key = lambda x : (x[0], x[1], x[2]))

q = ''
start = 0
end = 0
tem1 = []
tem2 = []
gap = 50

for i in a:

    if i[0] != q:

        if tem1:

            if tem1 not in tem2:
                tem2.append(tem1)
                tem1 = []

        q = I[0]
        start = int(i[1])
        end = int(i[2])
        continue

    if int(i[1]) < end or int(i[1]) - end < gap:
        if int(i[2]) > end:
            end = int(i[2])
            continue
        else:
            continue

    tem1.append([q,start,end])
    start = int(i[1])
    end = int(i[2])


with open ('new_result.txt','w')as f:

    for i in tem2:
        for o in I:
            print (o[0],o[1],o[2],file=f)

    for i in result:
        print (i[0],i[1],i[2],file=f)

如果觉得写得不错或者对你有帮助,请不要忘记点赞➕关注,评论区期待你的留言Good day!

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