You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hi,
I am trying to predict the HLA-B using the pre-fitted model and got the following output.
I do not understand why there are 72.6% missing SNPs for the Pos+Allele matching type. Is that a normal phenomenon, given the highly polymorphic properties in HLA regions?
My raw dataset was genotyped using Global Screening Array and I used the corresponding model.
Thank you in advance.
###############Output#########
HIBAG model for HLA-B:
500 individual classifiers
791 SNPs
88 unique HLA alleles: 07:02, 07:04, 07:05, ...
Prediction:
based on the averaged posterior probabilities
Model assembly: hg19, SNP assembly: hg19
Matching the SNPs between the model and the test data:
match.type="--" missing SNPs #
Position 26 (3.3%) being used [1]
Pos+Allele 574 (72.6%)* [2]
RefSNP+Position 27 (3.4%)
RefSNP 27 (3.4%)
[1]: useful if ambiguous strands on array-based platforms
[2]: suggested if the model and test data have been matched to the same reference genome
Model platform: Illumina 1M Duo / Infinium Global Screening Array
of SNP loci with flipped alleles: 367
of SNP loci with swapped strands: 365
of samples: 4050
CPU flags: 64-bit
of threads: 8
The text was updated successfully, but these errors were encountered:
Hi,
I am trying to predict the HLA-B using the pre-fitted model and got the following output.
I do not understand why there are 72.6% missing SNPs for the Pos+Allele matching type. Is that a normal phenomenon, given the highly polymorphic properties in HLA regions?
My raw dataset was genotyped using Global Screening Array and I used the corresponding model.
Thank you in advance.
###############Output#########
HIBAG model for HLA-B:
500 individual classifiers
791 SNPs
88 unique HLA alleles: 07:02, 07:04, 07:05, ...
Prediction:
based on the averaged posterior probabilities
Model assembly: hg19, SNP assembly: hg19
Matching the SNPs between the model and the test data:
match.type="--" missing SNPs #
Position 26 (3.3%) being used [1]
Pos+Allele 574 (72.6%)* [2]
RefSNP+Position 27 (3.4%)
RefSNP 27 (3.4%)
[1]: useful if ambiguous strands on array-based platforms
[2]: suggested if the model and test data have been matched to the same reference genome
Model platform: Illumina 1M Duo / Infinium Global Screening Array
of SNP loci with flipped alleles: 367
of SNP loci with swapped strands: 365
of samples: 4050
CPU flags: 64-bit
of threads: 8
The text was updated successfully, but these errors were encountered: