Hi Joel,
I ran the program on the example dataset using the code suggested in the help menu.
run.startmrca(vcf.file="FIN_chr2_pos136608646.vcf.gz",
- rec.file="decode_recmap_sexaveraged.txt",
- sample.ids="sample_ids.txt",
- refsample.ids="sample_ids.txt",
- mut.rate=1.6e-8,
- nsel=50,
- nanc=20,
- chain.length=20,
- nanc.post=10,
- pos=136608646,
- sel.allele=1)
The output is shown below:
[1] "Getting data from the vcf."
[1] "Removing variable sites with duplicated ID in the vcf (only the first sites are kept)."
[1] "Selected allele carrier IDs are specified."
Read 105 items
[1] "Reference panel IDs are specified."
[1] "Reference panel is the same as the carrier panel."
|======================================================================| 100%
[1] "Estimating the ancestral haplotype."
[1] "Getting the recombination map."
|======================================================================| 100%
[1] "Initializing the MCMC."
[1] "Starting the MCMC."
| | 0%Error in if (acceptance.ratio >= 0) { :
missing value where TRUE/FALSE needed
Is there any idea?
Thanks!
Lanhui
Hi Joel,
I ran the program on the example dataset using the code suggested in the help menu.
The output is shown below:
[1] "Getting data from the vcf."
[1] "Removing variable sites with duplicated ID in the vcf (only the first sites are kept)."
[1] "Selected allele carrier IDs are specified."
Read 105 items
[1] "Reference panel IDs are specified."
[1] "Reference panel is the same as the carrier panel."
|======================================================================| 100%
[1] "Estimating the ancestral haplotype."
[1] "Getting the recombination map."
|======================================================================| 100%
[1] "Initializing the MCMC."
[1] "Starting the MCMC."
| | 0%Error in if (acceptance.ratio >= 0) { :
missing value where TRUE/FALSE needed
Is there any idea?
Thanks!
Lanhui