zzh
/
gatk-3.8
1
0
Fork 0
Code Issues Pull Requests Packages Projects Releases Wiki Activity

Simple change to handle a no-call (must avoid asking for the second allele, which will be be null in this case). Also, added a hack to deal with input VCFs where there are no genotype likelihoods (needed in order to process Hapmap and 1KG VCFs). In this mode, called genotypes are assigned a likelihood of 0.96, and alternative genotypes are given 0.02 each. I know Beagle actually takes genotype data without likelihoods, so this might not be the right way to do this. 

git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@4081 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
kiran 2010-08-23 05:13:09 +00:00
parent dec713a184
commit 295472bf69
2 changed files with 24 additions and 1 deletions
Show Stats Download Patch File Download Diff File Expand all files Collapse all files

5
java/src/org/broadinstitute/sting/playground/gatk/walkers/BeagleOutputToVCFWalker.java
View File

@ -204,7 +204,7 @@ public class BeagleOutputToVCFWalker extends RodWalker<Integer, Integer> {
ArrayList<String> beagleGenotypePairs = beaglePhasedFeature.getGenotypes().get(sample);
Allele originalAlleleA = g.getAllele(0);
Allele originalAlleleB = g.getAllele(1);
Allele originalAlleleB = (g.getAlleles().size() == 2) ? g.getAllele(1) : g.getAllele(0); // hack to deal with no-call genotypes
// We have phased genotype in hp. Need to set the isRef field in the allele.
List<Allele> alleles = new ArrayList<Allele>();
@ -213,6 +213,9 @@ public class BeagleOutputToVCFWalker extends RodWalker<Integer, Integer> {
String alleleB = beagleGenotypePairs.get(1);
byte[] r = alleleA.getBytes();
//System.out.println(context.getLocation() + " : " + alleleA + " " + alleleB);
byte rA = r[0];
Boolean isRefA = (refByte == rA);

20
java/src/org/broadinstitute/sting/playground/gatk/walkers/ProduceBeagleInputWalker.java
View File

@ -148,6 +148,26 @@ public class ProduceBeagleInputWalker extends RodWalker<Integer, Integer> {
beagleGenotypesWriter.format("%c %c ", a, b);
}
}
else if (genotype.isCalled() && !genotype.hasAttribute(VCFConstants.GENOTYPE_LIKELIHOODS_KEY)) {
// hack to deal with input VCFs with no genotype likelihoods. Just assume the called genotype
// is confident. This is useful for Hapmap and 1KG release VCFs.
double AA = 0.02;
double AB = 0.02;
double BB = 0.02;
if (genotype.isHomRef()) { AA = 0.96; }
else if (genotype.isHet()) { AB = 0.96; }
else if (genotype.isHomVar()) { BB = 0.96; }
beagleWriter.printf("%.2f %.2f %.2f ", AA, AB, BB);
if (beagleGenotypesWriter != null) {
char a = genotype.getAllele(0).toString().charAt(0);
char b = genotype.getAllele(0).toString().charAt(0);
beagleGenotypesWriter.format("%c %c ", a, b);
}
}
else {
beagleWriter.print("0.33 0.33 0.33 "); // write 1/3 likelihoods for uncalled genotypes.
if (beagleGenotypesWriter != null)