Ejemplo n.º 1
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 def test_haploid_allele_indices_for_genotype_likelihood_index(self):
   for aix in six.moves.xrange(20):
     allele_indices = (aix,)
     ix = variant_utils.genotype_likelihood_index(allele_indices)
     actual = variant_utils.allele_indices_for_genotype_likelihood_index(
         ix, ploidy=1)
     self.assertEqual(actual, aix)
Ejemplo n.º 2
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 def test_haploid_allele_indices_for_genotype_likelihood_index(self):
   for aix in xrange(20):
     allele_indices = (aix,)
     ix = variant_utils.genotype_likelihood_index(allele_indices)
     actual = variant_utils.allele_indices_for_genotype_likelihood_index(
         ix, ploidy=1)
     self.assertEqual(actual, aix)
Ejemplo n.º 3
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 def test_diploid_allele_indices_for_genotype_likelihood_index(self):
   for aix in range(20):
     for bix in range(20):
       allele_indices = (aix, bix)
       expected = tuple(sorted(allele_indices))
       ix = variant_utils.genotype_likelihood_index(allele_indices)
       actual = variant_utils.allele_indices_for_genotype_likelihood_index(
           ix, ploidy=2)
       self.assertEqual(actual, expected)
Ejemplo n.º 4
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  def add(self, allele_indices, likelihood):
    """Add some likelihood to a particular allele configuration.

    Args:
      allele_indices: Pair of (g1, g2) ints representing the genotype.
      likelihood: float. log10(probability of this genotype configuration).
    """
    ix = variant_utils.genotype_likelihood_index(allele_indices)
    self._genotype_likelihood_containers[ix].append(likelihood)
Ejemplo n.º 5
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 def test_diploid_allele_indices_for_genotype_likelihood_index(self):
   for aix in xrange(20):
     for bix in xrange(20):
       allele_indices = (aix, bix)
       expected = tuple(sorted(allele_indices))
       ix = variant_utils.genotype_likelihood_index(allele_indices)
       actual = variant_utils.allele_indices_for_genotype_likelihood_index(
           ix, ploidy=2)
       self.assertEqual(actual, expected)
Ejemplo n.º 6
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  def __init__(self, num_alts):
    """Constructor.

    Args:
      num_alts: int. The number of alternate alleles in the variant.
    """
    self._num_likelihoods = variant_utils.genotype_likelihood_index(
        (num_alts, num_alts)) + 1

    # At each GL index, we keep a list that will include the joint GL across all
    # variants that include that particular set of allele indices for this
    # variant.
    self._genotype_likelihood_containers = []
    for _ in xrange(self._num_likelihoods):
      self._genotype_likelihood_containers.append([])