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Paul D. Blischak

dblp:214/1293 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2018
0000-0001-9177-8958ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › statistical genetics › genotype calling
genotype likelihood estimation
0.312018
SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data · Bioinform. 2018
Bioinformatics and computational biology › systems biology
parameter estimation
0.312018
SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data · Bioinform. 2018
Bioinformatics and computational biology › population genetics
population genomics
0.312018
SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data · Bioinform. 2018

Methods — techniques the papers use, named apart from their topics

maximum likelihood · 0.3genotype likelihood · 0.3
YearPublicationVenuePosition
2018 SNP genotyping and parameter estimation in polyploids using low-coverage sequencing data
abstract
Motivation: Genotyping and parameter estimation using high throughput sequencing data are everyday tasks for population geneticists, but methods developed for diploids are typically not applicable to polyploid taxa. This is due to their duplicated chromosomes, as well as the complex patterns of allelic exchange that often accompany whole genome duplication (WGD) events. For WGDs within a single lineage (autopolyploids), inbreeding can result from mixed mating and/or double reduction. For WGDs that involve hybridization (allopolyploids), alleles are typically inherited through independently segregating subgenomes. Results: We present two new models for estimating genotypes and population genetic parameters from genotype likelihoods for auto- and allopolyploids. We then use simulations to compare these models to existing approaches at varying depths of sequencing coverage and ploidy levels. These simulations show that our models typically have lower levels of estimation error for genotype and parameter estimates, especially when sequencing coverage is low. Finally, we also apply these models to two empirical datasets from the literature. Overall, we show that the use of genotype likelihoods to model non-standard inheritance patterns is a promising approach for conducting population genomic inferences in polyploids. Availability and implementation: A C ++ program, EBG, is provided to perform inference using the models we describe. It is available under the GNU GPLv3 on GitHub: https://github.com/pblischak/polyploid-genotyping. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online.
Paul D. Blischak, Laura Salter Kubatko, Andrea D. Wolfe
Bioinform.1