2020
DOI: 10.1007/s00122-020-03673-2
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Sequencing depth and genotype quality: accuracy and breeding operation considerations for genomic selection applications in autopolyploid crops

Abstract: Key message Polypoid crop breeders can balance resources between density and sequencing depth, dosage information and fewer highly informative SNPs recommended, non-additive models and QTL advantages on prediction dependent on trait architecture. Abstract The autopolyploid nature of potato and sweetpotato ensures a wide range of meiotic configurations and linkage phases leading to complex gene-action and pose problems in genotype data quality and genomic selection analyses. We used a 315-progeny biparental F… Show more

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Cited by 32 publications
(23 citation statements)
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“…This explains the observed correlation levels and provides genetic basis to improve more than one trait concurrently. These loci can be investigated further for putative genes and markers linked to haplotypes of interest for marker-assisted selection, or for leveraging QTL-informed genomic prediction models (Gemenet et al, 2020b). However, these strategies need to be validated in populations with broader genetic bases.…”
Section: Qtl Mapping For β-Carotene Iron and Zincmentioning
confidence: 99%
“…This explains the observed correlation levels and provides genetic basis to improve more than one trait concurrently. These loci can be investigated further for putative genes and markers linked to haplotypes of interest for marker-assisted selection, or for leveraging QTL-informed genomic prediction models (Gemenet et al, 2020b). However, these strategies need to be validated in populations with broader genetic bases.…”
Section: Qtl Mapping For β-Carotene Iron and Zincmentioning
confidence: 99%
“…We then established conditions for library preparation with these markers to reach high genotyping rates on either one of two sequencing platforms: Miseq or Nextseq. Reliable genotyping data in diploid plants requires a sequencing depth of at least 30 reads ( Gemenet et al, 2020 ). Based on our sequencing coverage from pooled samples, we estimate that 1,500 samples can be analyzed in one Miseq lane and 13,000 samples in one Nextseq lane for 96 target loci, each represented by one GT-seq marker.…”
Section: Discussionmentioning
confidence: 99%
“…WGS uses high coverage short reads to examine the homogeneity between the reference genome and short reads. Sequencing depth is an important parameter that determines the sensitivity and reproducibility in detecting variations among genomes [ 28 , 29 ]. In this work, we proposed a minimum of 20 × sequencing depth for mutation detection.…”
Section: Discussionmentioning
confidence: 99%