Mercurial > repos > miller-lab > genome_diversity
view pca.py @ 34:f739a296a339
Update to Miller Lab devshed revision 09dc81dbebc5
author | Richard Burhans <burhans@bx.psu.edu> |
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date | Mon, 23 Sep 2013 13:37:19 -0400 |
parents | 8997f2ca8c7a |
children |
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#!/usr/bin/env python import gd_util import os import re import shutil import sys from BeautifulSoup import BeautifulSoup import gd_composite ################################################################################ def do_ped2geno(input, output): lines = [] with open(input) as fh: for line in fh: line = line.rstrip('\r\n') lines.append(line.split()) pair_map = { '0':{ '0':'9', '1':'9', '2':'9' }, '1':{ '0':'1', '1':'2', '2':'1' }, '2':{ '0':'1', '1':'1', '2':'0' } } with open(output, 'w') as ofh: for a_idx in xrange(6, len(lines[0]), 2): b_idx = a_idx + 1 print >> ofh, ''.join(map(lambda line: pair_map[line[a_idx]][line[b_idx]], lines)) def do_map2snp(input, output): with open(output, 'w') as ofh: with open(input) as fh: for line in fh: elems = line.split() print >> ofh, ' {0} 11 0.002 2000 A T'.format(elems[1]) def make_ind_file(ind_file, input): pops = [] name_map = [] name_idx = 0 ofh = open(ind_file, 'w') with open(input) as fh: soup = BeautifulSoup(fh) misc = soup.find('div', {'id': 'gd_misc'}) populations = misc('ul')[0] i = 0 for entry in populations: if i % 2 == 1: population_name = entry.contents[0].encode('utf8').strip().replace(' ', '_') pops.append(population_name) individuals = entry.ol('li') for individual in individuals: individual_name = individual.string.encode('utf8').strip() name_map.append(individual_name) print >> ofh, 'ind_%s' % name_idx, 'M', population_name name_idx += 1 i += 1 ofh.close() return pops, name_map def make_par_file(par_file, geno_file, snp_file, ind_file, evec_file, eval_file): with open(par_file, 'w') as fh: print >> fh, 'genotypename: {0}'.format(geno_file) print >> fh, 'snpname: {0}'.format(snp_file) print >> fh, 'indivname: {0}'.format(ind_file) print >> fh, 'evecoutname: {0}'.format(evec_file) print >> fh, 'evaloutname: {0}'.format(eval_file) print >> fh, 'altnormstyle: NO' print >> fh, 'numoutevec: 2' def do_smartpca(par_file): prog = 'smartpca' args = [ prog ] args.append('-p') args.append(par_file) stdoutdata, stderrdata = gd_util.run_program(prog, args) stats = [] save_line = False for line in stdoutdata.split('\n'): if line.startswith(('## Average divergence', '## Anova statistics', '## Statistical significance')): stats.append('') save_line = True if line.strip() == '': save_line = False if save_line: stats.append(line) return '\n'.join(stats[1:]) def do_ploteig(evec_file, population_names): prog = 'gd_ploteig' args = [ prog ] args.append('-i') args.append(evec_file) args.append('-c') args.append('1:2') args.append('-p') args.append(':'.join(population_names)) args.append('-x') gd_util.run_program(prog, args) def do_eval2pct(eval_file, explained_file): prog = 'eval2pct' args = [ prog ] args.append(eval_file) with open(explained_file, 'w') as fh: gd_util.run_program(prog, args, stdout=fh) def do_coords2admix(coords_file): prog = 'coords2admix' args = [ prog ] args.append(coords_file) with open('fake', 'w') as fh: gd_util.run_program(prog, args, stdout=fh) shutil.copy2('fake', coords_file) ind_regex = re.compile('ind_([0-9]+)') def fix_names(name_map, files): for file in files: tmp_filename = '%s.tmp' % file with open(tmp_filename, 'w') as ofh: with open(file) as fh: for line in fh: line = line.rstrip('\r\n') match = ind_regex.search(line) if match: idx = int(match.group(1)) old = 'ind_%s' % idx new = name_map[idx].replace(' ', '_') line = line.replace(old, new) print >> ofh, line shutil.copy2(tmp_filename, file) os.unlink(tmp_filename) ################################################################################ if len(sys.argv) != 5: gd_util.die('Usage') input, input_files_path, output, output_files_path = sys.argv[1:5] gd_util.mkdir_p(output_files_path) ################################################################################ ped_file = os.path.join(input_files_path, 'admix.ped') geno_file = os.path.join(output_files_path, 'admix.geno') do_ped2geno(ped_file, geno_file) ################################################################################ map_file = os.path.join(input_files_path, 'admix.map') snp_file = os.path.join(output_files_path, 'admix.snp') do_map2snp(map_file, snp_file) ################################################################################ ind_file = os.path.join(output_files_path, 'admix.ind') population_names, name_map = make_ind_file(ind_file, input) ################################################################################ par_file = os.path.join(output_files_path, 'par.admix') evec_file = os.path.join(output_files_path, 'coordinates.txt') eval_file = os.path.join(output_files_path, 'admix.eval') make_par_file(par_file, geno_file, snp_file, ind_file, evec_file, eval_file) ################################################################################ smartpca_stats = do_smartpca(par_file) fix_names(name_map, [ind_file, evec_file]) ################################################################################ do_ploteig(evec_file, population_names) plot_file = 'coordinates.txt.1:2.{0}.pdf'.format(':'.join(population_names)) output_plot_file = os.path.join(output_files_path, 'PCA.pdf') shutil.copy2(plot_file, output_plot_file) os.unlink(plot_file) ################################################################################ do_eval2pct(eval_file, os.path.join(output_files_path, 'explained.txt')) os.unlink(eval_file) ################################################################################ do_coords2admix(evec_file) ################################################################################ info_page = gd_composite.InfoPage() info_page.set_title('PCA Galaxy Composite Dataset') display_file = gd_composite.DisplayFile() display_value = gd_composite.DisplayValue() out_pdf = gd_composite.Parameter(name='PCA.pdf', value='PCA.pdf', display_type=display_file) out_evec = gd_composite.Parameter(name='coordinates.txt', value='coordinates.txt', display_type=display_file) out_explained = gd_composite.Parameter(name='explained.txt', value='explained.txt', display_type=display_file) evec_prefix = 'coordinates.txt.1:2.{0}'.format(':'.join(population_names)) ps_file = '{0}.ps'.format(evec_prefix) xtxt_file = '{0}.xtxt'.format(evec_prefix) os.unlink(os.path.join(output_files_path, ps_file)) os.unlink(os.path.join(output_files_path, xtxt_file)) info_page.add_output_parameter(out_pdf) info_page.add_output_parameter(out_evec) info_page.add_output_parameter(out_explained) in_admix = gd_composite.Parameter(name='par.admix', value='par.admix', display_type=display_file) in_geno = gd_composite.Parameter(name='admix.geno', value='admix.geno', display_type=display_file) in_snp = gd_composite.Parameter(name='admix.snp', value='admix.snp', display_type=display_file) in_ind = gd_composite.Parameter(name='admix.ind', value='admix.ind', display_type=display_file) info_page.add_input_parameter(in_admix) info_page.add_input_parameter(in_geno) info_page.add_input_parameter(in_snp) info_page.add_input_parameter(in_ind) misc_stats = gd_composite.Parameter(description='Stats<p/><pre>\n{0}\n</pre>'.format(smartpca_stats), display_type=display_value) info_page.add_misc(misc_stats) with open (output, 'w') as ofh: print >> ofh, info_page.render() sys.exit(0)