Comments (3)
Hi, due to how the genotyping algorithm is designed it will unfortunately not scale well too that many samples. What you could do instead is to combine all predicted variants across all 500 samples and then run BayesTyper on each sample independently or in batches using this combined variants set. See here for more information: https://github.com/bioinformatics-centre/BayesTyper/wiki/Executing-BayesTyper-on-sample-batches
Please let me know if you have any other questions.
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@jonassibbesen I followed the method “Executing BayesTyper on sample batches” to genotyping my samples, when I Combine the the batch vcf files using bcftools merge, Error occured:
Failed to open bayestyper_rmdup_DH_00_unit_1/bayestyper-sk-b73.vcf.gz: not compressed with bgzip
it seems like bayestypre use gzip to commpress the vcf files, But bcftools require bgzip commpressed vcf files
from bayestyper.
Thank you for mentioning this. I have updated the wiki with an additional bgzip compression step.
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Related Issues (20)
- Question of the format of VCF file for BayesTyper. HOT 2
- A question about convertAllele.
- Questions about bayesTyperTools combine HOT 4
- Genotyping 500 samples
- Genotyping for the inversions HOT 2
- A question about VCF format of results from the 'genotype' function. HOT 1
- Identifying SV type from output HOT 1
- when cmake, Could NOT find Boost (missing: Boost_INCLUDE_DIR iostreams program_options system filesystem serialization) HOT 1
- Where are the test cases HOT 1
- how to run bayestyper HOT 2
- Classifying kmers error with bayesTyper 1.4.1 and 1.5 HOT 1
- Questions on data bundle and SV genotyping HOT 1
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- downloading variation priors fails HOT 3
- how to generate test cases
- genotype failed: Assertion `parameters.first > 0' failed. HOT 3
- What is the open source protocol for bayesTyper? HOT 1
- If executed multiple times, will the result of the data generated be the same each time? HOT 5
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