Closed stuartwillis closed 3 years ago
What does summary(myloci)
return? It shoud return the allele and genotype frequencies for all loci.
If your initial data are in a data frame (say DF), you can simply do myloci <- as.loci(DF)
(no need to go through a genind object).
It looks like what I would expect, e.g.
Locus Ots_IL8R_C8 : -- Genotype frequencies: C/C C/T T/T 4448 1167 737 -- Allele frequencies: C T 10063 2641
Locus Ots_unk3513_49 : -- Genotype frequencies: C/C C/T T/T 522 2341 3494 -- Allele frequencies: C T 3385 9329
Turns out 'as.loci' throws an error, but cycling through genind was successful, though that may have something to do with my problem
myloci2<-as.loci(for_linkage,allele.sep = ",") summary(myloci2) Error in tabulate(object[[i]], ng) : 'bin' must be numeric or a factor
head(for_linkage[,1:5]) Ots_myoD_364 Ots_u07_25_325 Ots_redd1_187 Ots_129458_451 Ots_crRAD21115_24 OtsBonn18-042618-2.06 G,G T,T A,A T,C C,C OtsBonn18-042718-1.02 G,G T,T A,A C,C C,C OtsBonn18-042718-1.04 G,G T,C A,A C,C C,C OtsBonn18-042718-2.03 G,G T,T A,A C,C C,C OtsBonn18-042718-2.04 T,G T,C A,G C,C C,C OtsBonn18-042718-2.06 G,G T,C A,A C,C C,T
I copied the lines after head(for_linkage[,1:5])
, pasted them into a text file (x.txt) and the followings worked well for me:
R> x <- read.loci("x.txt", allele.sep = ",")
R> x
Allelic data frame: 6 individuals
5 loci
R> str(x)
Classes ‘loci’ and 'data.frame': 6 obs. of 5 variables:
$ Ots_myoD_364 : Factor w/ 2 levels "G/G","G/T": 1 1 1 1 2 1
$ Ots_u07_25_325 : Factor w/ 2 levels "C/T","T/T": 2 2 1 2 1 1
$ Ots_redd1_187 : Factor w/ 2 levels "A/A","A/G": 1 1 1 1 2 1
$ Ots_129458_451 : Factor w/ 2 levels "C/C","C/T": 2 1 1 1 1 1
$ Ots_crRAD21115_24: Factor w/ 2 levels "C/C","C/T": 1 1 1 1 1 2
- attr(*, "locicol")= int [1:5] 1 2 3 4 5
R> summary(x)
Locus Ots_myoD_364:
-- Genotype frequencies:
G/G G/T
5 1
-- Allele frequencies:
G T
11 1
Locus Ots_u07_25_325:
-- Genotype frequencies:
..................................................... etc.................
I'm trying to calculate LD among ~250 SNPs in a large (6k) sample of individuals. The data are converted from a dataframe by df2genind and then to loci as genind2loci. However, when I run LD2 on the any two loci, I get
$Delta C T A NA NA G NA NA
$T2 T2 df P-val NA 1 NA
As far as I can tell the formatting is the same as the "jaguar" dataset (which runs ok),
And clearly the SNP states are being transferred correctly. Any ideas?