Mercurial > repos > rnateam > rnacommender
view rbpfeatures.py @ 3:ecf125a1ad73 draft
planemo upload for repository https://github.com/bgruening/galaxytools/tree/rna_commander/tools/rna_tools/rna_commender commit fb1fc1e3a062adfb1a78cd46aafd6a6e9f1e3bab
author | rnateam |
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date | Tue, 19 Jul 2016 10:22:02 -0400 |
parents | 8918de535391 |
children | a609d6dc8047 |
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"""Compute the RBP features.""" import re import subprocess as sp import uuid from os import mkdir from os import listdir from os.path import isfile, join from os import devnull from shutil import rmtree import numpy as np import pandas as pd import fasta_utils import pfam_utils __author__ = "Gianluca Corrado" __copyright__ = "Copyright 2016, Gianluca Corrado" __license__ = "MIT" __maintainer__ = "Gianluca Corrado" __email__ = "gianluca.corrado@unitn.it" __status__ = "Production" class RBPVectorizer(): """Compute the RBP features.""" def __init__(self, fasta): """ Constructor. Parameters ---------- fasta : str Fasta file containing the RBP sequences to predict. """ self.fasta = fasta self._mod_fold = "AURA_Human_data/RBP_features/mod" self._reference_fisher_scores = \ "AURA_Human_data/RBP_features/fisher_scores_ref" self._train_rbps_file = \ "AURA_Human_data/RBP_features/rbps_in_train.txt" self._temp_fold = "temp_" + str(uuid.uuid4()) self.pfam_scan = "%s/pfam_scan.txt" % self._temp_fold self._dom_fold = "%s/domains" % self._temp_fold self._seeds_fold = "%s/seeds" % self._temp_fold self._fisher_fold = "%s/fisher_scores" % self._temp_fold def _pfam_scan(self): """Scan the sequences against the Pfam database.""" nf = open(self.pfam_scan, "w") nf.write(pfam_utils.search_header()) fasta = fasta_utils.import_fasta(self.fasta) for rbp in sorted(fasta.keys()): seq = fasta[rbp] text = pfam_utils.sequence_search(rbp, seq) nf.write(text) nf.close() def _overlapping_domains(self): """Compute the set of domains contributing to the similarity.""" reference_domains = set([dom.replace(".mod", "") for dom in listdir(self._mod_fold) if isfile(join(self._mod_fold, dom))]) data = pfam_utils.read_pfam_output(self.pfam_scan) if data is None: return [] prot_domains = set([a.split('.')[0] for a in data["hmm_acc"]]) dom_list = sorted(list(reference_domains & prot_domains)) return dom_list def _prepare_domains(self, dom_list): """Select domain subsequences from the entire protein sequences.""" def prepare_domains(fasta_dic, dom_list, pfam_scan, out_folder): out_file_dic = {} for acc in dom_list: out_file_dic[acc] = open("%s/%s.fa" % (out_folder, acc), "w") f = open(pfam_scan) f.readline() for line in f: split = line.split() rbp = split[0] start = int(split[3]) stop = int(split[4]) acc = split[5].split('.')[0] if acc in out_file_dic.keys(): out_file_dic[acc].write( ">%s:%i-%i\n%s\n" % (rbp, start, stop, fasta_dic[rbp][start:stop])) f.close() for acc in dom_list: out_file_dic[acc].close() mkdir(self._dom_fold) fasta = fasta_utils.import_fasta(self.fasta) prepare_domains(fasta, dom_list, self.pfam_scan, self._dom_fold) def _compute_fisher_scores(self, dom_list): """Wrapper for SAM 3.5 get_fisher_scores.""" def get_fisher_scores(dom_list, mod_fold, dom_fold, fisher_fold): for acc in dom_list: _FNULL = open(devnull, 'w') cmd = "get_fisher_scores run -i %s/%s.mod -db %s/%s.fa" % ( mod_fold, acc, dom_fold, acc) fisher = sp.check_output( cmd, shell=True, stderr=_FNULL) nf = open("%s/%s.txt" % (fisher_fold, acc), "w") nf.write(fisher) nf.close() mkdir(self._fisher_fold) get_fisher_scores(dom_list, self._mod_fold, self._dom_fold, self._fisher_fold) def _ekm(self, dom_list): """Compute the empirical kernel map from the Fisher scores.""" def process_seg(e): """Process segment of a SAM 3.5 get_fisher_scores output file.""" seg = e.split() c = seg[0].split(':')[0] m = map(float, seg[3:]) return c, m def read_sam_file(samfile): """Read a SAM 3.5 get_fisher_scores output file.""" f = open(samfile) data = f.read() f.close() columns = [] m = [] split = re.split(">A ", data)[1:] for e in split: c, m_ = process_seg(e) columns.append(c) m.append(m_) m = np.matrix(m) df = pd.DataFrame(data=m.T, columns=columns) return df def dom_features(fisher_fold, dom_list, names=None): """Compute the features with respect to a domain type.""" dfs = [] for acc in dom_list: df = read_sam_file("%s/%s.txt" % (fisher_fold, acc)) df = df.groupby(df.columns, axis=1).mean() dfs.append(df) con = pd.concat(dfs, ignore_index=True) if names is not None: add = sorted(list(set(names) - set(con.columns))) fil = sorted(list(set(names) - set(add))) con = con[fil] for c in add: con[c] = np.zeros(len(con.index), dtype='float64') con = con[names] con = con.fillna(0.0) return con f = open(self._train_rbps_file) train_rbps = f.read().strip().split('\n') f.close() ref = dom_features(self._reference_fisher_scores, dom_list, names=train_rbps) ekm_ref = ref.T.dot(ref) ekm_ref.index = ekm_ref.columns sel = dom_features(self._fisher_fold, dom_list) ekm_sel = sel.T.dot(sel) ekm_sel.index = ekm_sel.columns ekm = ref.T.dot(sel) for rs in ekm.columns: for rr in ekm.index: if ekm_ref[rr][rr] > 0 and ekm_sel[rs][rs] > 0: ekm[rs][rr] /= np.sqrt(ekm_ref[rr][rr] * ekm_sel[rs][rs]) return ekm def vectorize(self): """Produce the RBP features.""" # create a temporary folder mkdir(self._temp_fold) # scan the RBP sequences against Pfam self._pfam_scan() # determine the accession numbers of the pfam domains needed for # computing the features dom_list = self._overlapping_domains() if len(dom_list) == 0: rmtree(self._temp_fold) return None # prepare fasta file with the sequence of the domains self._prepare_domains(dom_list) # compute fisher scores using SAM 3.5 self._compute_fisher_scores(dom_list) # compute the empirical kernel map ekm = self._ekm(dom_list) # remove the temporary folder rmtree(self._temp_fold) return ekm