2020
DOI: 10.1007/s10592-020-01307-0
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Detecting genomic variation underlying phenotypic characteristics of reintroduced Coho salmon (Oncorhynchus kisutch)

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Cited by 11 publications
(13 citation statements)
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“…Mapping, alignment trimming, and filtering to the charr reference genome were performed with BWA-MEM v 0.7.12, SAMtools v 1.5 using a mapping quality threshold of 10, and SAMblaster v 0.1.24 (Faust & Hall, 2014), while filtering for a quality score threshold of 20 was performed by BBMap v 37.93 (Bushnell, sourceforge.net/projects/bbmap/, accessed 20-11-2019), and summarized with Fastqc v 0.11.7 (Andrews, 2010). SNP filtering was carried out using common parameters for salmonid species, found below (Horn et al, 2020). Duplicate sequences and unpaired reads were filtered using SAMtools, BBMap, and Picard tools with a minimum fastq trimming length of 25 bp.…”
Section: Pool-seq Pipeline and Snp Discoverymentioning
confidence: 99%
“…Mapping, alignment trimming, and filtering to the charr reference genome were performed with BWA-MEM v 0.7.12, SAMtools v 1.5 using a mapping quality threshold of 10, and SAMblaster v 0.1.24 (Faust & Hall, 2014), while filtering for a quality score threshold of 20 was performed by BBMap v 37.93 (Bushnell, sourceforge.net/projects/bbmap/, accessed 20-11-2019), and summarized with Fastqc v 0.11.7 (Andrews, 2010). SNP filtering was carried out using common parameters for salmonid species, found below (Horn et al, 2020). Duplicate sequences and unpaired reads were filtered using SAMtools, BBMap, and Picard tools with a minimum fastq trimming length of 25 bp.…”
Section: Pool-seq Pipeline and Snp Discoverymentioning
confidence: 99%
“…Genomic DNA was extracted from 286 fish using a Chelex extraction method (Sweet et al, 1996). Libraries were prepared with NEBNext Ultra kits with a modified version of the protocol to reduce reaction volumes (see detailed protocol in Horn et al, 2020). Briefly here, DNA of each sample was first quantified and normalized, before being randomly fragmented using dsDNA fragmentase (NEB, We used the "PPalign" module in the PoolParty pipeline to perform bioinformatics .…”
Section: Whole Genome Resequencing and Snp Detectionmentioning
confidence: 99%
“…Our approach to genome resequencing was to target low read depth for individually barcoded samples and then to combine sequence reads from individuals of the same phenotype for further analyses of the four groups: resident male, anadromous male, resident female, and anadromous female. To prepare the libraries for whole-genome resequencing, individuals were barcoded, and a NEBNext Ultra enzymatic fragmentation protocol was followed ( Horn et al, 2020 ). Briefly, we extracted DNA according to a Chelex extraction method ( Sweet et al, 1996 ).…”
Section: Methodsmentioning
confidence: 99%