Comments (3)
I realize now that a potential workaround is to specify --no-fixchr-truth and --no-fixchr-query and -l [list of contig names], which seems to work for me. A little cumbersome, perhaps, but workable ;)
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Yes, I actually have a ticket for version 0.2.8 to make this easier.
The reason for the current behaviour is to simplify switching between hg19 (which has chr prefixes) and GRCH37 (which doesn't). For the purposes of Platinum Genomes comparisons (which are done on chr1-22), these two are equivalent.
If neither test_input.vcf.gz nor test_calls.vcf.gz contain contigs with a chr prefix, hap.py should automatically decide to not change the chromosome prefix however. If it still does, then this is a bug.
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Version 0.2.8 detects numeric chromosome names from the reference fasta file, so the switches above should not be necessary anymore.
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Related Issues (20)
- Parsing results VCF gives different counts of TRUTH FN than summary HOT 1
- CMake Error at CMakeLists.txt:32 (message): Building external dependencies has failed
- Error running BCFTOOLS :Argument list too long
- Integrating vcfdist as a comparison engine into hap.py
- missing reference HOT 1
- VCF format issues with --write-vcf, - FORMAT field inconsistencies HOT 1
- Trying to print sequence when we mean contig name
- error code 1
- Docker Implementation: Several Error Messages Related to "preprocess" HOT 1
- ROC and PR curve HOT 2
- Docker fails to build for both bases
- Incorrect number of FORMAT/AD values on scmp-distance engine
- Link provide in email is broken HOT 1
- [E::bgzf_uncompress] inflate failed: invalid distance too far back HOT 1
- Docker build failed HOT 1
- How is the false positive rate calculated in som.py stats?
- Can't find reference HOT 1
- While using hap.py, there is a problem:
- Make a new pre-built docker image?
- Using --usefiltered-truth results in incorrect FP calls for filtered variants in the truth (xcmp)
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