Mercurial > repos > gregory-minevich > snp_mapping_using_wgs
comparison SNP_Mapping.py @ 38:7fb9d1e732a0 draft default tip
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author | gregory-minevich |
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date | Fri, 19 Sep 2014 16:37:08 -0400 |
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37:6841f9837250 | 38:7fb9d1e732a0 |
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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() |