Detection and mapping of mtDNA SNPs in Atlantic salmon using high throughput DNA sequencing

Approximately half of the mitochondrial genome inherent within 546 individual Atlantic salmon (Salmo salar) derived from across the species' North Atlantic range, was selectively amplified with a novel combination of standard PCR and pyro-sequencing in a single run using 454 Titanium FLX techno...

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Bibliographic Details
Published in:BMC Genomics
Main Authors: Fridjonsson, Olafur, Olafsson, Kristinn, Tompsett, Scott, Bjornsdottir, Snaedis, Consuegra, Sonia, Knox, David, de Leaniz, Carlos Garcia, Magnusdottir, Steinunn, Olafsdottir, Gudbjorg, Verspoor, Eric, Hjorleifsdottir, Sigridur
Format: Article in Journal/Newspaper
Language:English
Published: 2011
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Online Access:https://pure.uhi.ac.uk/en/publications/9475298d-7536-448e-84d8-b424b4dec118
https://doi.org/10.1186/1471-2164-12-179
Description
Summary:Approximately half of the mitochondrial genome inherent within 546 individual Atlantic salmon (Salmo salar) derived from across the species' North Atlantic range, was selectively amplified with a novel combination of standard PCR and pyro-sequencing in a single run using 454 Titanium FLX technology (Roche, 454 Life Sciences). A unique combination of barcoded primers and a partitioned sequencing plate was employed to designate each sequence read to its original sample. The sequence reads were aligned according to the S. salar mitochondrial reference sequence (NC_001960.1), with the objective of identifying single nucleotide polymorphisms (SNPs). They were validated if they met with the following three stringent criteria: (i) sequence reads were produced from both DNA strands; (ii) SNPs were confirmed in a minimum of 90% of replicate sequence reads; and (iii) SNPs occurred in more than one individual.