comparison SNP_Mapping.py @ 38:7fb9d1e732a0 draft default tip

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author gregory-minevich
date Fri, 19 Sep 2014 16:37:08 -0400
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37:6841f9837250 38:7fb9d1e732a0
1 #!/usr/bin/python
2
3 import re
4 import sys
5 import optparse
6 import csv
7 import re
8 import pprint
9 from decimal import *
10 from rpy import *
11
12 def main():
13 csv.field_size_limit(1000000000)
14
15 parser = optparse.OptionParser()
16 parser.add_option('-v', '--sample_vcf', dest = 'sample_vcf', action = 'store', type = 'string', default = None, help = "Sample VCF from GATK Unified Genotyper")
17 parser.add_option('-l', '--loess_span', dest = 'loess_span', action = 'store', type = 'float', default = .1, help = "Loess span")
18 parser.add_option('-d', '--d_yaxis', dest = 'd_yaxis', action = 'store', type = 'float', default = 1, help = "y-axis upper limit for dot plot")
19 parser.add_option('-y', '--h_yaxis', dest = 'h_yaxis', action = 'store', type = 'int', default = 0, help = "y-axis upper limit for histogram plot")
20 parser.add_option('-c', '--points_color', dest = 'points_color', action = 'store', type = 'string', default = "gray27", help = "Color for data points")
21 parser.add_option('-k', '--loess_color', dest = 'loess_color', action = 'store', type = 'string', default = "red", help = "Color for loess regression line")
22 parser.add_option('-z', '--standardize', dest = 'standardize', default= 'true', help = "Standardize X-axis")
23 parser.add_option('-b', '--break_file', dest = 'break_file', action = 'store', type = 'string', default = 'C.elegans', help = "File defining the breaks per chromosome")
24 parser.add_option('-x', '--bin_size', dest = 'bin_size', action = 'store', type = 'int', default = 1000000, help = "Size of histogram bins, default is 1mb")
25 parser.add_option('-n', '--normalize_bins', dest = 'normalize_bins', default= 'true', help = "Normalize histograms")
26
27
28 parser.add_option('-o', '--output', dest = 'output', action = 'store', type = 'string', default = None, help = "Output file name")
29 parser.add_option('-s', '--location_plot_output', dest = 'location_plot_output', action = 'store', type = 'string', default = "SNP_Mapping_Plot.pdf", help = "Output file name of SNP plots by chromosomal location")
30
31 (options, args) = parser.parse_args()
32
33 vcf_info = parse_vcf(sample_vcf = options.sample_vcf)
34
35 output_vcf_info(output = options.output, vcf_info = vcf_info)
36
37 rounded_bin_size = int(round((float(options.bin_size) / 1000000), 1) * 1000000)
38
39 normalized_histogram_bins_per_mb = calculate_normalized_histogram_bins_per_xbase(vcf_info = vcf_info, xbase = rounded_bin_size, normalize_bins = options.normalize_bins)
40 max_y_hist_mb = normalized_histogram_bins_per_mb[max(normalized_histogram_bins_per_mb, key = lambda x: normalized_histogram_bins_per_mb.get(x) )]
41
42 normalized_histogram_bins_per_5kb = calculate_normalized_histogram_bins_per_xbase(vcf_info = vcf_info, xbase = (rounded_bin_size / 2), normalize_bins = options.normalize_bins)
43 max_y_hist_5kb = normalized_histogram_bins_per_5kb[max(normalized_histogram_bins_per_5kb, key = lambda x: normalized_histogram_bins_per_5kb.get(x) )]
44
45 max_y_hist_overall = myround(max(max_y_hist_mb, max_y_hist_5kb) + int(round(round(max(max_y_hist_mb, max_y_hist_5kb)) * .1)))
46
47 break_dict = parse_breaks(break_file = options.break_file)
48
49 output_scatter_plots_by_location(location_plot_output = options.location_plot_output, vcf_info = vcf_info, loess_span=options.loess_span, d_yaxis=options.d_yaxis, h_yaxis=options.h_yaxis, points_color=options.points_color, loess_color=options.loess_color, standardize =options.standardize, normalized_hist_per_mb = normalized_histogram_bins_per_mb, normalized_hist_per_5kb = normalized_histogram_bins_per_5kb, breaks = break_dict, rounded_bin_size = rounded_bin_size, max_y_hist_overall = max_y_hist_overall)
50
51
52 def myround(x, base=10):
53 return int(base * round(float(x)/base))
54
55 def skip_headers(reader = None, i_file = None):
56 # count headers
57 comment = 0
58 while reader.next()[0].startswith('#'):
59 comment = comment + 1
60
61 # skip headers
62 i_file.seek(0)
63 for i in range(0, comment):
64 reader.next()
65
66 def parse_breaks(break_file = None):
67 if break_file == 'C.elegans':
68 break_dict = { 'I' : 16 , 'II' : 16, 'III' : 14, 'IV' : 18, 'V' : 21, 'X' : 18 }
69 return break_dict
70 elif break_file == 'Brachypodium':
71 break_dict = { '1' : 75 , '2' : 60, '3' : 60, '4' : 50, '5' : 30 }
72 return break_dict
73 elif break_file == 'Arabidopsis':
74 break_dict = { '1' : 31 , '2' : 20, '3' : 24, '4' : 19, '5' : 27 }
75 return break_dict
76 else:
77 i_file = open(break_file, 'rU')
78 break_dict = {}
79 reader = csv.reader(i_file, delimiter = '\t')
80 for row in reader:
81 chromosome = row[0].upper()
82 chromosome = re.sub("CHROMOSOME_", "", chromosome, flags = re.IGNORECASE)
83 chromosome = re.sub("chr", "", chromosome, flags = re.IGNORECASE)
84 #Brachy
85 chromosome = re.sub("Bd", "", chromosome, flags = re.IGNORECASE)
86 chromosome = re.sub("bd", "", chromosome, flags = re.IGNORECASE)
87
88 break_count = row[1]
89 break_dict[chromosome] = int(break_count)
90 return break_dict
91
92
93 def location_comparer(location_1, location_2):
94 chr_loc_1 = location_1.split(':')[0]
95 pos_loc_1 = int(location_1.split(':')[1])
96
97 chr_loc_2 = location_2.split(':')[0]
98 pos_loc_2 = int(location_2.split(':')[1])
99
100 if chr_loc_1 == chr_loc_2:
101 if pos_loc_1 < pos_loc_2:
102 return -1
103 elif pos_loc_1 == pos_loc_1:
104 return 0
105 elif pos_loc_1 > pos_loc_2:
106 return 1
107 elif chr_loc_1 < chr_loc_2:
108 return -1
109 elif chr_loc_1 > chr_loc_2:
110 return 1
111
112 def output_vcf_info(output = None, vcf_info = None):
113 o_file = open(output, 'wb')
114 writer = csv.writer(o_file, delimiter = '\t')
115
116 writer.writerow(["#Chr\t", "Pos\t", "Alt Count\t", "Ref Count\t", "Read Depth\t", "Ratio\t"])
117
118 location_sorted_vcf_info_keys = sorted(vcf_info.keys(), cmp=location_comparer)
119
120 for location in location_sorted_vcf_info_keys:
121 alt_allele_count, ref_allele_count, read_depth, ratio = vcf_info[location]
122
123 location_info = location.split(':')
124 chromosome = location_info[0]
125 position = location_info[1]
126
127 writer.writerow([chromosome, position, alt_allele_count, ref_allele_count, read_depth, ratio])
128
129 o_file.close()
130
131 def output_scatter_plots_by_location(location_plot_output = None, vcf_info = None, loess_span="", d_yaxis="", h_yaxis="", points_color="", loess_color="", standardize=None, normalized_hist_per_mb = None, normalized_hist_per_5kb = None, breaks = None, rounded_bin_size = 1000000, max_y_hist_overall = ""):
132 positions = {}
133 current_chr = ""
134 prev_chr = ""
135
136 x_label = "Location (Mb)"
137 filtered_label = ''
138
139 location_sorted_vcf_info_keys = sorted(vcf_info.keys(), cmp=location_comparer)
140
141 break_unit = Decimal(rounded_bin_size) / Decimal(1000000)
142 max_breaks = max(breaks.values())
143
144 try:
145 r.pdf(location_plot_output, 8, 8)
146
147 for location in location_sorted_vcf_info_keys:
148 current_chr = location.split(':')[0]
149 position = location.split(':')[1]
150
151 alt_allele_count, ref_allele_count, read_depth, ratio = vcf_info[location]
152
153 if prev_chr != current_chr:
154 if prev_chr != "":
155 hist_dict_mb = get_hist_dict_by_chr(normalized_hist_per_xbase = normalized_hist_per_mb, chr = prev_chr)
156 hist_dict_5kb = get_hist_dict_by_chr(normalized_hist_per_xbase = normalized_hist_per_5kb, chr = prev_chr)
157
158 if h_yaxis == 0:
159 plot_data(chr_dict = positions, hist_dict_mb = hist_dict_mb, hist_dict_5kb = hist_dict_5kb, chr = prev_chr + filtered_label, x_label = "Location (Mb)", divide_position = True, draw_secondary_grid_lines = True, loess_span=loess_span, d_yaxis=d_yaxis, h_yaxis=max_y_hist_overall, points_color=points_color, loess_color=loess_color, breaks = breaks[prev_chr], standardize=standardize, max_breaks = max_breaks, break_unit = break_unit)
160 else:
161 plot_data(chr_dict = positions, hist_dict_mb = hist_dict_mb, hist_dict_5kb = hist_dict_5kb, chr = prev_chr + filtered_label, x_label = "Location (Mb)", divide_position = True, draw_secondary_grid_lines = True, loess_span=loess_span, d_yaxis=d_yaxis, h_yaxis=h_yaxis, points_color=points_color, loess_color=loess_color, breaks = breaks[prev_chr], standardize=standardize, max_breaks = max_breaks, break_unit = break_unit)
162
163 prev_chr = current_chr
164 positions = {}
165
166 positions[position] = ratio
167
168 hist_dict_mb = get_hist_dict_by_chr(normalized_hist_per_xbase = normalized_hist_per_mb, chr = current_chr)
169 hist_dict_5kb = get_hist_dict_by_chr(normalized_hist_per_xbase = normalized_hist_per_5kb, chr = current_chr)
170
171 if h_yaxis == 0:
172 plot_data(chr_dict = positions, hist_dict_mb = hist_dict_mb, hist_dict_5kb = hist_dict_5kb, chr = current_chr + filtered_label, x_label = "Location (Mb)", divide_position = True, draw_secondary_grid_lines = True, loess_span=loess_span, d_yaxis=d_yaxis, h_yaxis=max_y_hist_overall, points_color=points_color, loess_color=loess_color, breaks = breaks[current_chr], standardize=standardize, max_breaks = max_breaks, break_unit = break_unit)
173 else:
174 plot_data(chr_dict = positions, hist_dict_mb = hist_dict_mb, hist_dict_5kb = hist_dict_5kb, chr = current_chr + filtered_label, x_label = "Location (Mb)", divide_position = True, draw_secondary_grid_lines = True, loess_span=loess_span, d_yaxis=d_yaxis, h_yaxis=h_yaxis, points_color=points_color, loess_color=loess_color, breaks = breaks[current_chr], standardize=standardize, max_breaks = max_breaks, break_unit = break_unit)
175
176 r.dev_off()
177
178 except Exception as inst:
179 print inst
180 print "There was an error creating the location plot pdf... Please try again"
181
182 def get_hist_dict_by_chr(normalized_hist_per_xbase = None, chr = ''):
183 hist_dict = {}
184
185 for location in normalized_hist_per_xbase:
186 chromosome = location.split(':')[0]
187 if chromosome == chr:
188 position = int(location.split(':')[1])
189 hist_dict[position] = normalized_hist_per_xbase[location]
190
191 max_location = max(hist_dict.keys(), key=int)
192 for i in range(1, max_location):
193 if i not in hist_dict:
194 hist_dict[i] = 0
195
196 return hist_dict
197
198
199 def plot_data(chr_dict = None, hist_dict_mb = None, hist_dict_5kb = None, chr = "", x_label = "", divide_position = False, draw_secondary_grid_lines = False, loess_span=None, d_yaxis=None, h_yaxis=None, points_color="", loess_color="", breaks = None, standardize= None, max_breaks = 1, break_unit = 1):
200 ratios = "c("
201 positions = "c("
202
203 for position in chr_dict:
204 ratio = chr_dict[position]
205 if divide_position:
206 position = float(position) / 1000000.0
207 positions = positions + str(position) + ", "
208 ratios = ratios + str(ratio) + ", "
209
210 if len(ratios) == 2:
211 ratios = ratios + ")"
212 else:
213 ratios = ratios[0:len(ratios) - 2] + ")"
214
215 if len(positions) == 2:
216 positions = positions + ")"
217 else:
218 positions = positions[0:len(positions) - 2] + ")"
219
220 r("x <- " + positions)
221 r("y <- " + ratios)
222
223 hist_mb_values = "c("
224 for position in sorted(hist_dict_mb):
225 hist_mb_values = hist_mb_values + str(hist_dict_mb[position]) + ", "
226
227 if len(hist_mb_values) == 2:
228 hist_mb_values = hist_mb_values + ")"
229 else:
230 hist_mb_values = hist_mb_values[0:len(hist_mb_values) - 2] + ")"
231
232 hist_5kb_values = "c("
233 for position in sorted(hist_dict_5kb):
234 hist_5kb_values = hist_5kb_values + str(hist_dict_5kb[position]) + ", "
235
236 if len(hist_5kb_values) == 2:
237 hist_5kb_values = hist_5kb_values + ")"
238 else:
239 hist_5kb_values = hist_5kb_values[0:len(hist_5kb_values) - 2] + ")"
240
241 r("xz <- " + hist_mb_values)
242 r("yz <- " + hist_5kb_values)
243
244
245 max_break_str = str(max_breaks)
246 break_unit_str = str(Decimal(break_unit))
247 half_break_unit_str = str(Decimal(break_unit) / Decimal(2))
248 break_penta_unit_str = str(Decimal(break_unit) * Decimal(5))
249
250 if (standardize=='true'):
251 r("plot(x, y, cex=0.60, xlim=c(0," + max_break_str + "), main='LG " + chr + "', xlab= '" + x_label + "', ylim = c(0, %f " %d_yaxis + "), ylab='Percentage of mapping strain alleles/total reads (at SNP positions)', pch=10, col='"+ points_color +"')")
252 r("lines(loess.smooth(x, y, span = %f "%loess_span + "), lwd=5, col='"+ loess_color +"')")
253 r("axis(1, at=seq(0, " + max_break_str + ", by=" + break_unit_str + "), labels=FALSE, tcl=-0.5)")
254 r("axis(1, at=seq(0, " + max_break_str + ", by=" + half_break_unit_str + "), labels=FALSE, tcl=-0.25)")
255 r("axis(2, at=seq(floor(min(y)), 1, by=0.1), labels=FALSE, tcl=-0.2)")
256 elif (standardize=='false'):
257 r("plot(x, y, cex=0.60, main='LG " + chr + " ', xlab= '" + x_label + "', ylim = c(0, %f " %d_yaxis + "), ylab='Percentage of mapping strain alleles/total reads (at SNP positions)', pch=10, col='"+ points_color +"')")
258 r("lines(loess.smooth(x, y, span = %f "%loess_span + "), lwd=5, col='"+ loess_color +"')")
259 r("axis(1, at=seq(0, as.integer( ' " + str(breaks) + " '), by= " + break_unit_str + "), labels=FALSE, tcl=-0.5)")
260 r("axis(1, at=seq(0, as.integer( ' " + str(breaks) + " '), by= " + half_break_unit_str + "), labels=FALSE, tcl=-0.25)")
261 r("axis(2, at=seq(floor(min(y)), 1, by=0.1), labels=FALSE, tcl=-0.2)")
262
263 if draw_secondary_grid_lines:
264 r("abline(h = seq(floor(min(y)), 1, by=0.1), v = seq(floor(min(x)), length(x), by= 1), col='gray')")
265 else:
266 r("grid(lty = 1, col = 'gray')")
267
268 if (standardize=='true'):
269 #r("barplot(xz, xlim=c(0, " + max_break_str + "), ylim = c(0, " + str(h_yaxis) + "), yaxp=c(0, " + str(h_yaxis) + ", 1), space = 0, col='darkgray', width = " + break_unit_str + ", xlab='Location (Mb)', ylab='Normalized frequency of pure parental alleles ', main='LG " + chr + " (Hawaiian Variant Mapping)')")
270 r("barplot(xz, xlim=c(0, " + max_break_str + "), ylim = c(0, " + str(h_yaxis) + "), yaxp=c(0, " + str(h_yaxis) + ", 1), space = 0, col='darkgray', width = " + break_unit_str + ", xlab='Location (Mb)', ylab='Normalized frequency of pure parental alleles ', main='LG " + chr + "')")
271 r("barplot(yz, space = 0, add=TRUE, width = " + half_break_unit_str + ", col=rgb(1, 0, 0, 1))")
272 r("axis(1, hadj = 1, at=seq(0, " + max_break_str + ", by= " + break_unit_str + "), labels=FALSE, tcl=-0.5)")
273 r("axis(1, at=seq(0, " + max_break_str + ", by= " + break_penta_unit_str + "), labels=TRUE, tcl=-0.5)")
274 r("axis(1, at=seq(0, " + max_break_str + ", by= " + half_break_unit_str + "), labels=FALSE, tcl=-0.25)")
275 elif (standardize=='false'):
276 #r("barplot(xz, ylim = c(0, " + str(h_yaxis) + "), yaxp=c(0, " + str(h_yaxis) + ", 1), space = 0, col='darkgray', width = 1, xlab='Location (Mb)', ylab='Normalized frequency of pure parental alleles ', main='LG " + chr + " (Hawaiian Variant Mapping)')")
277 r("barplot(xz, ylim = c(0, " + str(h_yaxis) + "), yaxp=c(0, " + str(h_yaxis) + ", 1), space = 0, col='darkgray', width = 1, xlab='Location (Mb)', ylab='Normalized frequency of pure parental alleles ', main='LG " + chr + " ')")
278 r("barplot(yz, space = 0, add=TRUE, width = 0.5, col=rgb(1, 0, 0, 1))")
279 r("axis(1, at=seq(0, as.integer( ' " + str(breaks) + " '), by= " + break_unit_str + "), labels=FALSE, tcl=-0.5)")
280 r("axis(1, at=seq(0, as.integer( ' " + str(breaks) + " '), by= " + break_penta_unit_str + "), labels=TRUE, tcl=-0.5)")
281 r("axis(1, at=seq(0, as.integer( ' " + str(breaks) + " '), by= " + half_break_unit_str + "), labels=FALSE, tcl=-0.25)")
282
283
284
285 def calculate_normalized_histogram_bins_per_xbase(vcf_info = None, xbase = 1000000, normalize_bins = None):
286 normalized_histogram_bins_per_xbase = {}
287
288 ref_snp_count_per_xbase = get_ref_snp_count_per_xbase(vcf_info = vcf_info, xbase = xbase)
289
290 mean_zero_snp_count_per_chromosome = get_mean_zero_snp_count_per_chromosome(vcf_info = vcf_info, xbase = xbase)
291
292 zero_snp_count_per_xbase = get_zero_snp_count_per_xbase(vcf_info = vcf_info, xbase = xbase)
293
294
295 for location in ref_snp_count_per_xbase:
296 chromosome = location.split(':')[0]
297 mean_zero_snp_count = mean_zero_snp_count_per_chromosome[chromosome]
298 ref_snp_count = ref_snp_count_per_xbase[location]
299
300 zero_snp_count = 0
301 if location in zero_snp_count_per_xbase:
302 zero_snp_count = zero_snp_count_per_xbase[location]
303
304 if normalize_bins == 'true':
305 if zero_snp_count == 0 or ref_snp_count == 0:
306 normalized_histogram_bins_per_xbase[location] = 0
307 elif zero_snp_count == ref_snp_count:
308 normalized_histogram_bins_per_xbase[location] = 0
309 else:
310 normalized_histogram_bins_per_xbase[location] = (Decimal(zero_snp_count) / (Decimal(ref_snp_count)-Decimal(zero_snp_count))) * Decimal(mean_zero_snp_count)
311 else:
312 normalized_histogram_bins_per_xbase[location] = zero_snp_count
313
314 return normalized_histogram_bins_per_xbase
315
316
317 def get_ref_snp_count_per_xbase(vcf_info = None, xbase = 1000000):
318 ref_snps_per_xbase = {}
319
320 for location in vcf_info:
321 location_info = location.split(':')
322
323 chromosome = location_info[0].upper()
324 chromosome = re.sub("CHROMOSOME_", "", chromosome, flags = re.IGNORECASE)
325 chromosome = re.sub("chr", "", chromosome, flags = re.IGNORECASE)
326
327 #Brachy
328 chromosome = re.sub("Bd", "", chromosome, flags = re.IGNORECASE)
329 chromosome = re.sub("bd", "", chromosome, flags = re.IGNORECASE)
330
331 position = location_info[1]
332 xbase_position = (int(position) / xbase) + 1
333
334 location = chromosome + ":" + str(xbase_position)
335 if location in ref_snps_per_xbase:
336 ref_snps_per_xbase[location] = ref_snps_per_xbase[location] + 1
337 else:
338 ref_snps_per_xbase[location] = 1
339
340 return ref_snps_per_xbase
341
342
343
344 def get_mean_zero_snp_count_per_chromosome(vcf_info, xbase = 1000000):
345 sample_snp_count_per_xbase = {}
346
347 for location in vcf_info:
348 alt_allele_count, ref_allele_count, read_depth, ratio = vcf_info[location]
349
350 location_info = location.split(':')
351 chromosome = location_info[0]
352 position = location_info[1]
353 xbase_position = (int(position) / xbase) + 1
354 xbase_location = chromosome + ":" + str(xbase_position)
355
356 if int(alt_allele_count) == 0:
357 if xbase_location in sample_snp_count_per_xbase:
358 sample_snp_count_per_xbase[xbase_location] = sample_snp_count_per_xbase[xbase_location] + 1
359 else:
360 sample_snp_count_per_xbase[xbase_location] = 1
361
362 elif int(alt_allele_count) != 0 and xbase_location not in sample_snp_count_per_xbase:
363 sample_snp_count_per_xbase[xbase_location] = 0
364
365 mean_zero_snp_count_per_chromosome = {}
366 for location in sample_snp_count_per_xbase:
367 chromosome = location.split(':')[0]
368 sample_count = sample_snp_count_per_xbase[location]
369 if chromosome in mean_zero_snp_count_per_chromosome:
370 mean_zero_snp_count_per_chromosome[chromosome].append(sample_count)
371 else:
372 mean_zero_snp_count_per_chromosome[chromosome] = [sample_count]
373
374 for chromosome in mean_zero_snp_count_per_chromosome:
375 summa = sum(mean_zero_snp_count_per_chromosome[chromosome])
376 count = len(mean_zero_snp_count_per_chromosome[chromosome])
377
378 mean_zero_snp_count_per_chromosome[chromosome] = Decimal(summa) / Decimal(count)
379
380 return mean_zero_snp_count_per_chromosome
381
382
383 def get_zero_snp_count_per_xbase(vcf_info = None, xbase = 1000000):
384 zero_snp_count_per_xbase = {}
385
386 for location in vcf_info:
387 alt_allele_count, ref_allele_count, read_depth, ratio = vcf_info[location]
388
389 location_info = location.split(':')
390 chromosome = location_info[0]
391 position = location_info[1]
392 xbase_position = (int(position) / xbase) + 1
393 xbase_location = chromosome + ":" + str(xbase_position)
394
395 if int(alt_allele_count) == 0:
396 if xbase_location in zero_snp_count_per_xbase:
397 zero_snp_count_per_xbase[xbase_location] = zero_snp_count_per_xbase[xbase_location] + 1
398 else:
399 zero_snp_count_per_xbase[xbase_location] = 1
400
401 elif int(alt_allele_count) != 0 and xbase_location not in zero_snp_count_per_xbase:
402 zero_snp_count_per_xbase[xbase_location] = 0
403
404 return zero_snp_count_per_xbase
405
406
407 def parse_vcf(sample_vcf = None):
408 i_file = open(sample_vcf, 'rU')
409 reader = csv.reader(i_file, delimiter = '\t', quoting = csv.QUOTE_NONE)
410
411 skip_headers(reader = reader, i_file = i_file)
412 vcf_info = {}
413
414 for row in reader:
415 chromosome = row[0].upper()
416 chromosome = re.sub("CHROMOSOME_", "", chromosome, flags = re.IGNORECASE)
417 chromosome = re.sub("chr", "", chromosome, flags = re.IGNORECASE)
418
419 #Brachy
420 chromosome = re.sub("Bd", "", chromosome, flags = re.IGNORECASE)
421 chromosome = re.sub("bd_", "", chromosome, flags = re.IGNORECASE)
422
423 if chromosome != 'MTDNA':
424 position = row[1]
425 #ref_allele = row[2]
426 #read_depth = row[3]
427 #read_bases = row[4]
428
429 vcf_format_info = row[8].split(":")
430 vcf_allele_freq_data = row[9]
431
432 read_depth_data_index = vcf_format_info.index("DP")
433 read_depth = vcf_allele_freq_data.split(":")[read_depth_data_index]
434
435 ref_and_alt_counts_data_index = vcf_format_info.index("AD")
436 ref_and_alt_counts = vcf_allele_freq_data.split(":")[ref_and_alt_counts_data_index]
437 ref_allele_count = ref_and_alt_counts.split(",")[0]
438 alt_allele_count = ref_and_alt_counts.split(",")[1]
439
440 location = chromosome + ":" + position
441
442 if (Decimal(read_depth)!=0):
443 getcontext().prec = 6
444 ratio = Decimal(alt_allele_count) / Decimal(read_depth)
445
446 vcf_info[location] = (alt_allele_count, ref_allele_count, read_depth, ratio)
447
448 #debug line
449 #print chromosome, position, read_depth, ref_allele_count, alt_allele_count, ratio, id
450
451 i_file.close()
452
453 return vcf_info
454
455 def parse_read_bases(read_bases = None, alt_allele = None):
456 read_bases = re.sub('\$', '', read_bases)
457 read_bases = re.sub('\^[^\s]', '', read_bases)
458
459 ref_allele_matches = re.findall("\.|\,", read_bases)
460 ref_allele_count = len(ref_allele_matches)
461
462 alt_allele_matches = re.findall(alt_allele, read_bases, flags = re.IGNORECASE)
463 alt_allele_count = len(alt_allele_matches)
464
465 #debug line
466 #print read_bases, alt_allele, alt_allele_count, ref_allele_count
467
468 return ref_allele_count, alt_allele_count
469
470 if __name__ == "__main__":
471 main()