Description Usage Arguments Value Author(s) References See Also
View source: R/updog_genotype.R
Uses alelle counts to reestimate genotypes with updog approach and stores the genotypes probabilities or for further multipoint analysis
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vcfR.object |
object output of the vcfR package |
onemap.object |
object of class onemap |
vcf.par |
Field of VCF that informs the depth of alleles |
parent1 |
parent 1 identification in vcfR object |
parent2 |
parent 2 identification in vcfR objetc |
f1 |
f1 individual identification if f2 cross type |
recovering |
logical defining if markers should be recovered from VCF |
mean_phred |
the mean phred score of the sequencer technology |
cores |
number of threads |
depths |
list containing a matrix for ref and other for alt allele counts, samples ID in colum and markers ID in rows |
global_error |
number from 0 to 1 defining the global error to be considered together with the genotype errors or the genotype probabilities or NULL to not considered any global error |
use_genotypes_errors |
if |
rm_multiallelic |
if |
use_genotype_probs |
if |
onemap object with genotypes updated
Cristiane Taniguti, chtaniguti@usp.br
Gerard, D., Ferrão L.F.V., Garcia, A.A.F., & Stephens, M. (2018). Harnessing Empirical Bayes and Mendelian Segregation for Genotyping Autopolyploids from Messy Sequencing Data. bioRxiv. doi: 10.1101/281550.
extract_depth
binom_genotype
and
https://github.com/dcgerard/updog.
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