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What can we infer about mutation calling by using time‐series mutation accumulation data and a Bayesian Mutation Finder?
by
Freeman, Jack
, Maruki, Takahiro
, Ozere, April
, Cristescu, Melania E.
in
Accumulation
/ Bayesian analysis
/ Bayesian Mutation Finder
/ Daphnia pulex
/ Data analysis
/ Estimates
/ Evolutionary Ecology
/ Gene sequencing
/ Genomes
/ Genomic analysis
/ Genomics
/ Genotype & phenotype
/ Genotypes
/ Mutation
/ mutation rate
/ Mutation rates
/ Nucleotides
/ Organisms
/ Parameter identification
/ Propagation
/ single nucleotide mutations
/ time‐series mutation accumulation data
/ Whole genome sequencing
2024
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What can we infer about mutation calling by using time‐series mutation accumulation data and a Bayesian Mutation Finder?
by
Freeman, Jack
, Maruki, Takahiro
, Ozere, April
, Cristescu, Melania E.
in
Accumulation
/ Bayesian analysis
/ Bayesian Mutation Finder
/ Daphnia pulex
/ Data analysis
/ Estimates
/ Evolutionary Ecology
/ Gene sequencing
/ Genomes
/ Genomic analysis
/ Genomics
/ Genotype & phenotype
/ Genotypes
/ Mutation
/ mutation rate
/ Mutation rates
/ Nucleotides
/ Organisms
/ Parameter identification
/ Propagation
/ single nucleotide mutations
/ time‐series mutation accumulation data
/ Whole genome sequencing
2024
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What can we infer about mutation calling by using time‐series mutation accumulation data and a Bayesian Mutation Finder?
by
Freeman, Jack
, Maruki, Takahiro
, Ozere, April
, Cristescu, Melania E.
in
Accumulation
/ Bayesian analysis
/ Bayesian Mutation Finder
/ Daphnia pulex
/ Data analysis
/ Estimates
/ Evolutionary Ecology
/ Gene sequencing
/ Genomes
/ Genomic analysis
/ Genomics
/ Genotype & phenotype
/ Genotypes
/ Mutation
/ mutation rate
/ Mutation rates
/ Nucleotides
/ Organisms
/ Parameter identification
/ Propagation
/ single nucleotide mutations
/ time‐series mutation accumulation data
/ Whole genome sequencing
2024
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What can we infer about mutation calling by using time‐series mutation accumulation data and a Bayesian Mutation Finder?
Journal Article
What can we infer about mutation calling by using time‐series mutation accumulation data and a Bayesian Mutation Finder?
2024
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Overview
Accurate estimates of mutation rates derived from genome‐wide mutation accumulation (MA) data are fundamental to understanding basic evolutionary processes. The rapidly improving high‐throughput sequencing technologies provide unprecedented opportunities to identify single nucleotide mutations across genomes. However, such MA derived data are often difficult to analyze and the performance of the available methods of analysis is not well understood. In this study, we used the existing Bayesian Genotype Caller adapted for MA data that we refer to as Bayesian Mutation Finder (BMF) for identifying single nucleotide mutations while considering the characteristics of the data. We compared the performance of BMF with the widely used Genome Analysis Toolkit (GATK) by applying these two methods to time‐series MA data as well as simulated data. The time‐series data were obtained by propagating Daphnia pulex over an average of 188 generations and performing whole‐genome sequencing of 14 MA lines across three time points. The results indicate that BMF enables more accurate identification of single nucleotide mutations than GATK especially when applied to the empirical data. Furthermore, BMF involves the use of fewer parameters and is more computationally efficient than GATK. Both BMF and GATK found surprisingly many candidate mutations that were not confirmed at later time points. We systematically infer causes of the unconfirmed candidate mutations, introduce a framework for estimating mutation rates based on genome‐wide candidate mutations confirmed by subsequent sequencing, and provide an improved mutation rate estimate for D. pulex. Considering the characteristics of mutation accumulation (MA) data, we adapted the existing Bayesian Genotype Caller and we call this Bayesian Mutation Finder (BMF). The performance comparison of BMF and the currently widely used Genome Analysis Toolkit (GATK) using empirical time‐series and simulated MA data indicates that BMF enables more accurate mutation calling than GATK especially when applied to empirical data.
Publisher
John Wiley & Sons, Inc,John Wiley and Sons Inc,Wiley
Subject
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