Parentage assignment with genotyping‐by‐sequencing data
Authors:
Open Access
- 13 December 2018
- journal article
- research article
- Published by Wiley in Journal of Animal Breeding and Genetics
- Vol. 136 (2) , 102-112
Abstract
In this paper, we evaluate using genotype‐by‐sequencing (GBS) data to perform parentage assignment in lieu of traditional array data. The use of GBS data raises two issues: First, for low‐coverage (e.g., 2×) GBS data performs similarly to array data and requires only a small number of markers to correctly assign parents and (b) low‐coverage GBS data (as low as 0.1×) can also be used, provided that it is obtained across a large number of markers. When analysing the low‐coverage GBS data, we also found a high number of false positives if the true parent is not contained within the list of candidate parents, but that this false positive rate can be greatly reduced by hand tuning the assignment threshold. We provide this parentage assignment method as a standalone program called AlphaAssign.Keywords
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Funding Information
- Biotechnology and Biological Sciences Research Council (BB/J004235/1, BB/L020467/1, BB/L020726/1, BB/M009254/1, BB/N004728/1, BB/N004736/1, BB/N006178/1)
- Medical Research Council (MR/M000370/1)
This publication has 31 references indexed in Scilit:
- Genotyping-by-Sequencing (GBS): A Novel, Efficient and Cost-Effective Genotyping Method for Cattle Using Next-Generation SequencingPLOS ONE, 2013
- Assessment of alternative genotyping strategies to maximize imputation accuracy at minimal costGenetics Selection Evolution, 2012
- MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesGenetic Epidemiology, 2010
- Persistence of accuracy of genome-wide breeding values over generations when including a polygenic effectGenetics Selection Evolution, 2009
- High-resolution haplotype block structure in the cattle genomeBMC Genomic Data, 2009
- FRANz: reconstruction of wild multi-generation pedigreesBioinformatics, 2009
- Fast and flexible simulation of DNA sequence dataGenome Research, 2008
- Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD MarkersPLOS ONE, 2008
- Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype ClusteringThe American Journal of Human Genetics, 2007
- Statistical confidence for likelihood‐based paternity inference in natural populationsMolecular Ecology, 1998