2019
DOI: 10.1111/tpj.14429
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Genome‐wide association study identified novel candidate loci affecting wood formation in Norway spruce

Abstract: SummaryNorway spruce is a boreal forest tree species of significant ecological and economic importance. Hence there is a strong imperative to dissect the genetics underlying important wood quality traits in the species. We performed a functional genome‐wide association study (GWAS) of 17 wood traits in Norway spruce using 178 101 single nucleotide polymorphisms (SNPs) generated from exome genotyping of 517 mother trees. The wood traits were defined using functional modelling of wood properties across annual gr… Show more

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Cited by 50 publications
(56 citation statements)
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“…A total of 1654 individuals (unrelated parents) originating from different latitudes across Sweden, were included in this study for analysis of the SNP variation following a latitudinal cline. Details regarding the DNA extraction, exome capture, genotyping and SNP annotation have been previously described in Baison et al (Baison et al , 2019). For the current analysis, trees were divided into six populations, S1-S6.…”
Section: Methodsmentioning
confidence: 99%
“…A total of 1654 individuals (unrelated parents) originating from different latitudes across Sweden, were included in this study for analysis of the SNP variation following a latitudinal cline. Details regarding the DNA extraction, exome capture, genotyping and SNP annotation have been previously described in Baison et al (Baison et al , 2019). For the current analysis, trees were divided into six populations, S1-S6.…”
Section: Methodsmentioning
confidence: 99%
“…Both trials were established in 1990 with a spacing 1.4m × 1.4 m. Originally, the experiments contained more than 12 progenies from 524 families at each of site, but after thinning activities in Höreda and Erikstorp in 2010 and 2008, respectively, fewer trees were left. In 2011 and 2012, six trees per site (524 * 12 ~ 6000 trees) were phenotyped 30 and the 524 mothers were genotyped using exome capture (single nucleotide polymorphism, SNP) 31 . Standing tree-based measurements with Pilodyn and Hitman were performed on the same trees in 2011 and 2013, respectively, after which further thinning was performed.…”
Section: Plant Materialsmentioning
confidence: 99%
“…Genotyping was conducted at Rapid Genomics, USA, using exom capture methodology. Sequence capture was performed using the 40 018 diploid probes previously designed and evaluated for P. abies 41 and samples were sequenced to an average depth of 15x using an Illumina HiSeq 2500 (San Diego, USA) 31 . Variant calling was performed using the Genome Analysis Toolkit (GATK) HaplotypeCaller 42 in Genome Variant Call Format (gVCF) output format.…”
Section: Genotypic Datamentioning
confidence: 99%
“…Genotyping was conducted at Rapid Genomics, USA, using exom capture methodology same as the method used in Baison et. al 2019 40 . Sequence capture was performed using the 40 018 diploid probes previously designed and evaluated for P. abies 41 and samples were sequenced to an average depth of 15x using an Illumina HiSeq 2500 (San Diego, USA) 40 .…”
Section: Genotypic Datamentioning
confidence: 99%
“…al 2019 40 . Sequence capture was performed using the 40 018 diploid probes previously designed and evaluated for P. abies 41 and samples were sequenced to an average depth of 15x using an Illumina HiSeq 2500 (San Diego, USA) 40 . Variant calling was performed using the Genome Analysis Toolkit (GATK) HaplotypeCaller v3.6 42 in Genome Variant Call Format (gVCF) output format.…”
Section: Genotypic Datamentioning
confidence: 99%