#!/usr/bin/python import os import sys import scipy.optimize.nnls import scipy.sparse import numpy as np from subprocess import * import argparse import platform def main(): parser = argparse.ArgumentParser(description= "Quikr returns the estimated frequencies of batcteria present when given a \ input FASTA file. \n \ A default trained matrix will be used if none is supplied \n \ You must supply a kmer and default lambda if using a custom trained \ matrix.") parser.add_argument("-f", "--fasta", help="path to a fasta file", required=True) parser.add_argument("-t", "--trained-matrix", help="path to a custom trained matrix") parser.add_argument("-l", "--lamb", type=int, help="the default lambda value is 10,000") parser.add_argument("-k", "--kmer", type=int, help="specifies which kmer to use, must be used with a custom trained database") args = parser.parse_args() # Do some basic sanity checks if not os.path.isfile(args.fasta): parser.error( "Input fasta file not found") # If we are using a custom trained matrix, we need to do some basic checks if args.trained_matrix is not None: if not os.path.isfile(args.trained_matrix): parser.error("custom trained matrix not be found") if args.kmer is None: parser.error("A kmer is required when using a custom matrix") else: kmer = args.kmer if args.lamb is None: # use 10,000 as default Lambda input_lambda = 10000 # If we aren't using a custom trained matrix, load in the defaults else: trained_matrix_location = "output.npy" input_lambda = 10000 kmer = 6 xstar = quikr(args.fasta, trained_matrix_location, kmer, input_lambda) return 0 def quikr(input_fasta_location, trained_matrix_location, kmer, default_lambda): """ input_fasta is the input fasta file to find the estimated frequencies of trained_matrix is the trained matrix we are using to estimate the species kmer is the desired k-mer to use default_lambda is inp returns the estimated requencies of bacteria present when given an input FASTA file of amplicon (454) reads. A k-mer based, L1 regularized, sparsity promoting algorthim is utilized. In practice reconstruction is accurate only down to the genus level (not species or strain). """ uname = platform.uname()[0] # We use the count program to count ____ if uname == "Linux" and os.path.isfile("./count-linux"): print "Detected Linux" count_input = Popen(["./count-linux", "-r", str(kmer), "-1", "-u", input_fasta_location], stdout=PIPE) elif uname == "Darwin" and os.path.isfile("./count-osx"): print "Detected Mac OS X" count_input = Popen(["count-osx", "-r", str(kmer), "-1", "-u", input_fasta_location], stdout=PIPE) # load the output of our count program and form a probability vector from the counts counts = np.loadtxt(count_input.stdout) counts = counts / np.sum(counts) counts = default_lambda * counts trained_matrix = np.load(trained_matrix_location) # perform the non-negative least squares # import pdb; pdb.set_trace() counts = np.rot90(counts) xstar = scipy.optimize.nnls(trained_matrix, counts) xstar = xstar / sum(xstar) return xstar if __name__ == "__main__": sys.exit(main())