I guess I should have mentioned that I have NGS data for the whole genome, and that's how I do my calls.
Does that review talk about doing it from reads?
Hello,
I have a highly polymorphic (10% polymorphism rate) genome. I expect this variation to be due to heterozygosity. What is the best way to try and phase my haplotypes?
Thank you.
EDIT: I found samtools has such a module called phase, and I phased my .bam file. However, I have no idea what to do with it to analyze the ouput. I wanted to be able to extract the build phased haplotypes and to measure their frequencies.
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What type of data do you have or plan to obtain?
I am trying to obtain haplotypes that are phased to see how my variants are linked with each other.
I am also trying to obtain haplotype frequencies.
Now my recommendation is to open a new question titled: "How does the samtools phase operation work?"
thank you, done.