Mercurial > repos > public-health-bioinformatics > assign_clades
comparison assign_clades.py @ 0:a971083404a4 draft default tip
planemo upload for repository https://github.com/Public-Health-Bioinformatics/flu_classification_suite commit b96b6e06f6eaa6ae8ef4c24630dbb72a4aed7dbe
author | public-health-bioinformatics |
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date | Thu, 04 Jul 2019 19:34:32 -0400 |
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-1:000000000000 | 0:a971083404a4 |
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1 #!/usr/bin/env python | |
2 | |
3 '''Accepts fasta files containing amino acid sequence, reading them in as | |
4 amino acid sequence objects. Reads influenza clade defintions (i.e. amino | |
5 acids at certain positions) from .csv file into dictionary structure. Searches | |
6 each of the amino acid sequence objects for a list of matching clades, assigns | |
7 the most 'evolved' (i.e. child as opposed to parent clade) to the sequence. Appends | |
8 "_cladename" to the Sequence name and generates a fasta file of original sequences with | |
9 modified names.''' | |
10 | |
11 '''Author: Diane Eisler, Molecular Microbiology & Genomics, BCCDC Public Health Laboratory, Oct 2017''' | |
12 | |
13 import sys,string,os, time, Bio | |
14 from Bio import Seq, SeqIO, SeqUtils, Alphabet, SeqRecord | |
15 from Bio.SeqRecord import SeqRecord | |
16 from Bio.Alphabet import IUPAC | |
17 from Bio.Seq import Seq | |
18 | |
19 localtime = time.asctime(time.localtime(time.time())) #date and time of analysis | |
20 inFileHandle1 = sys.argv[1] #batch fasta file with sequences to be parsed | |
21 inFileHandle2 = sys.argv[2] # .csv file containing clade definitions and "depth" | |
22 outFileHandle = sys.argv[3] #user-specified name for output file of aa seq's with clade suffixes | |
23 outFile= open(outFileHandle,'w') #open a writable, appendable output file | |
24 seqList = [] #list of aa sequence objects to parse for clade definitions | |
25 cladeList = [] #empty list to hold clade tuples i.e. ("3C.3a", 1 ,{"3":"I", "9":"V"..}) | |
26 | |
27 '''Searches record for required amino acids at defined positions. If found, assigns | |
28 clade name to sequence name by appending underscore and clade name to record id.''' | |
29 def call_clade(record): | |
30 print("---------------------------------------------------------------------") | |
31 print("Parsing %s for matching flu clade definitions..." % (record.id)) | |
32 matchList = [] #empty list to hold clades that match 100% | |
33 #iterate over each tuple in the clade list | |
34 for clade in cladeList: | |
35 cladeName = clade[0] #temp variable for name | |
36 depth = clade[1] #temp variable for depth | |
37 sites = clade[2] #temp variable for aa def dictionary | |
38 shouldFind = len(sites) #number of sites that should match | |
39 found = 0 #a counter to hold matches to antigenic sites | |
40 #iterate over each position in sites dictionary | |
41 for pos, aa in sites.items(): | |
42 #translate pos to corresponding index in target sequence | |
43 index = int(pos) - 1 | |
44 #if record at index has same amino acid as 'aa', increment 'found' | |
45 if record[index] == aa: | |
46 found += 1 | |
47 if (found == shouldFind): | |
48 #add the matching clade tuple to the list of matches | |
49 matchList.append(clade) | |
50 return matchList | |
51 | |
52 '''Compares depth level of clades in a list and returns the most granular one''' | |
53 def decide_clade_by_depth(matchList): | |
54 #empty variable for maximum depth encountered | |
55 max_depth = 0 | |
56 best_match_name = '' #variable to hold most granular clade | |
57 #for each matching clade, check depth of the corresponding tuple | |
58 for clade in matchList: | |
59 #if the current clade is 'deeper' than the one before it | |
60 if clade[1] > max_depth: | |
61 #store this depth | |
62 max_depth = clade[1] | |
63 #store name of the clade | |
64 best_match_name = clade[0] | |
65 return best_match_name | |
66 | |
67 '''opens the .csv file of clade definitions and clade "depth" ''' | |
68 with open (inFileHandle2, 'r') as clade_file: | |
69 #remove whitespace from the end of each line and split elements at commas | |
70 for line in clade_file: | |
71 #print "Current Line in File:" + line | |
72 sites={} #initialize a dictionary for clade | |
73 elementList = line.rstrip().split(',') | |
74 new_list = [] #start a new list to put non-empty strings into | |
75 #remove empty stings in list | |
76 for item in elementList: | |
77 if item != '': | |
78 new_list.append(item) | |
79 name = new_list.pop(0) #move 1st element to name field | |
80 depth = int(new_list.pop(0)) #move 2nd element to depth field | |
81 #read remaining pairs of non-null elements into clade def dictionary | |
82 for i in range(0, len(new_list), 2): | |
83 #move next 2 items from the list into the dict | |
84 pos = new_list[i] | |
85 aa = new_list[i + 1] | |
86 sites[pos] = aa | |
87 #add the clade info as a tuple to the cladeList[] | |
88 oneClade =(name, depth, sites) | |
89 cladeList.append(oneClade) | |
90 print("The List of Clades:") | |
91 for clade in cladeList: | |
92 print("Clade Name: %s Depth: %i Antigenic Sites: %i" % (clade[0], clade[1], len(clade[2]))) | |
93 for pos, aa in clade[2].items(): | |
94 print("Pos: %s\tAA: %s" % (pos,aa)) | |
95 | |
96 '''opens readable input file of sequences to parse using filename from cmd line, | |
97 instantiates as AA Sequence objects, with ppercase sequences''' | |
98 with open(inFileHandle1,'r') as inFile: | |
99 #read in Sequences from fasta file, uppercase and add to seqList | |
100 for record in SeqIO.parse(inFile, "fasta", alphabet=IUPAC.protein): | |
101 record = record.upper() | |
102 seqList.append(record) #add Seq to list of Sequences | |
103 print("\n%i flu HA sequences will be compared to current clade definitions..." % len(seqList)) | |
104 #parse each target sequence object | |
105 for record in seqList: | |
106 clade_call = '' #empty variale for final clade call on sequence | |
107 matchingCladeList = call_clade(record) #holds matching clade tuples | |
108 #if there is more than one clade match | |
109 if len(matchingCladeList) > 1: | |
110 #choose the most granular clade based on depth | |
111 clade_call = decide_clade_by_depth(matchingCladeList) | |
112 #if there is only one clade call | |
113 elif len(matchingCladeList) > 0: | |
114 clade = matchingCladeList[0] #take the first tuple in the list | |
115 clade_call = clade[0] #clade name is the first item in the tuple | |
116 #empty list return, no matches | |
117 else: | |
118 clade_call = "No_Match" | |
119 print(clade_call) | |
120 seq_name = record.id | |
121 mod_name = seq_name + "_" + clade_call | |
122 print("New Sequence Name: " + mod_name) | |
123 record.id = mod_name | |
124 | |
125 | |
126 #output fasta file with clade calls appended to sequence names | |
127 SeqIO.write(seqList,outFile,"fasta") | |
128 | |
129 #print("\n%i Sequences Extracted to Output file: %s" % ((len(extractedSeqList),outFileHandle))) | |
130 inFile.close() | |
131 clade_file.close() | |
132 outFile.close() | |
133 |