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I am using some methods for Hyphy positive selection. I have an alignment with 243 spp, and 2 individuals per species. For this reason, I have two different haplotypes per species. To reduce the complexity and time, I considered pooling the two haplotypes, but this will generate some ambiguous (IUPAC-symboled) nucleotides.
My question is the following: When entering a codon with a IUPAC symbol that represents two possible nucleotides, does Hyphy consider the two nucleotide options for the analyses, or does it treat the nucleotide as "missing data"? In this latter case, I would rather only choose one of the two haplotypes for the analysis.
Thanks in advance for your help.
Best,
Pol Sorigué
The text was updated successfully, but these errors were encountered:
HyPhy will treat nucleotide ambiguities as partially missing data (e.g. a Y maps to [0,1,0,1] probabilities for the corresponding leaf). Partially resolved codons work the same way, e.g. CRA ~ CAA or CGA.
Hi!
I am using some methods for Hyphy positive selection. I have an alignment with 243 spp, and 2 individuals per species. For this reason, I have two different haplotypes per species. To reduce the complexity and time, I considered pooling the two haplotypes, but this will generate some ambiguous (IUPAC-symboled) nucleotides.
My question is the following: When entering a codon with a IUPAC symbol that represents two possible nucleotides, does Hyphy consider the two nucleotide options for the analyses, or does it treat the nucleotide as "missing data"? In this latter case, I would rather only choose one of the two haplotypes for the analysis.
Thanks in advance for your help.
Best,
Pol Sorigué
The text was updated successfully, but these errors were encountered: