/* * The MIT License * * Copyright (c) 2015 The Broad Institute * * Permission is hereby granted, free of charge, to any person obtaining a copy * of this software and associated documentation files (the "Software"), to deal * in the Software without restriction, including without limitation the rights * to use, copy, modify, merge, publish, distribute, sublicense, and/or sell * copies of the Software, and to permit persons to whom the Software is * furnished to do so, subject to the following conditions: * * The above copyright notice and this permission notice shall be included in * all copies or substantial portions of the Software. * * THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR * IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY, * FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL THE * AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER * LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING FROM, * OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER DEALINGS IN * THE SOFTWARE. */ package picard.fingerprint; import htsjdk.variant.variantcontext.Allele; import picard.util.MathUtil; import java.util.List; /** * Represents the likelihood of the HaplotypeBlock given the GenotypeLikelihoods (GL field from a VCF, which is actually a log10-likelihood) * for each of the SNPs in that block. By convention the alleles stored for each SNP are in phase. * * @author Yossi Farjoun */ public class HaplotypeProbabilitiesFromGenotypeLikelihoods extends HaplotypeProbabilitiesUsingLogLikelihoods { public HaplotypeProbabilitiesFromGenotypeLikelihoods(final HaplotypeBlock haplotypeBlock) { super(haplotypeBlock); } /** * Adds a base observation with the observed quality to the evidence for this haplotype * based on the fact that the SNP is part of the haplotype. * * @param snp The snp in the haplotypeblock to which the likelihoods belong * @param alleles the (ordered) alleles to which the biallelic genotype likelihoods correspond. So that if the alleles are [A,B], the * @param logGenotypeLikelihoods correspond to the logLikelihoods of [AA, AB, BB]. Log is assumed to be in base 10. */ public void addToLogLikelihoods(final Snp snp, final List<Allele> alleles, final double[] logGenotypeLikelihoods) { assertSnpPartOfHaplotype(snp); // only allow biallelic snps assert (logGenotypeLikelihoods.length == Genotype.values().length); assert (alleles.size() == 2); //make sure that alleles are comparable to SNPs for (int i = 0; i < 2; i++) { assert (alleles.get(i).getBases().length == 1); } final byte allele1 = alleles.get(0).getBases()[0]; final byte allele2 = alleles.get(1).getBases()[0]; // alleles as given might be swapped with alleles in haplotype block. // if that is the case, swap them around. if (snp.getAllele1() == allele1 && snp.getAllele2() == allele2) { setLogLikelihoods(MathUtil.sum(getLogLikelihoods(),logGenotypeLikelihoods)); return; } if (snp.getAllele2() == allele1 && snp.getAllele1() == allele2) { final double [] ll = getLogLikelihoods(); ll[Genotype.HOM_ALLELE1.v] += logGenotypeLikelihoods[Genotype.HOM_ALLELE2.v]; ll[Genotype.HET_ALLELE12.v] += logGenotypeLikelihoods[Genotype.HET_ALLELE12.v]; ll[Genotype.HOM_ALLELE2.v] += logGenotypeLikelihoods[Genotype.HOM_ALLELE1.v]; setLogLikelihoods(ll); return; } // if we are here it means that there was a mismatch in alleles... assert true; } }