2011
DOI: 10.1007/s10709-011-9554-4
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Microsatellite standardization and evaluation of genotyping error in a large multi-partner research programme for conservation of Atlantic salmon (Salmo salar L.)

Abstract: Microsatellite genotyping is a common DNA characterization technique in population, ecological and evolutionary genetics research. Since different alleles are sized relative to internal size-standards, different laboratories must calibrate and standardize allelic designations when exchanging data. This interchange of microsatellite data can often prove problematic. Here, 16 microsatellite loci were calibrated and standardized for the Atlantic salmon, Salmo salar, across 12 laboratories. Although inconsistencie… Show more

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Cited by 73 publications
(82 citation statements)
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“…Inter-laboratory calibration for microsatellite markers is notoriously challenging due to the fact that the alleles are scored in a polymer matrix in relation to DNA fragments of known size (i.e., the size-standard), a process influenced by local instrument chemistry. Nevertheless, calibration of the standard set of microsatellite markers implemented in the NMDR has been previously achieved between four separate laboratories that have been involved with genotyping the samples upon which the register is based [11], and has for example also been achieved in a European project for Atlantic salmon ( Salmo salar L.) data coming from multiple laboratories [12]. In order to calibrate microsatellite analyses between the laboratories at ICR and IMR, samples have been exchanged as part of a previous study [6].…”
Section: Methodsmentioning
confidence: 99%
“…Inter-laboratory calibration for microsatellite markers is notoriously challenging due to the fact that the alleles are scored in a polymer matrix in relation to DNA fragments of known size (i.e., the size-standard), a process influenced by local instrument chemistry. Nevertheless, calibration of the standard set of microsatellite markers implemented in the NMDR has been previously achieved between four separate laboratories that have been involved with genotyping the samples upon which the register is based [11], and has for example also been achieved in a European project for Atlantic salmon ( Salmo salar L.) data coming from multiple laboratories [12]. In order to calibrate microsatellite analyses between the laboratories at ICR and IMR, samples have been exchanged as part of a previous study [6].…”
Section: Methodsmentioning
confidence: 99%
“…The DNA solution (10x) was used to genotype 15 microsatellite loci selected for the European SALSEA-Merge project [37]. A QIAGEN's Multiplex PCR Kit was used for PCR amplification according to manufacturer's recommendations, using an annealing temperature of 568C.…”
Section: (B) Genetic Analysesmentioning
confidence: 99%
“…Genomic DNA was extracted from fin samples in a solution with 10lL of proteinase K (10 mg/mL), 10 lL of TE (TrisEDTA 1X) and 100 lL of Chelex 100 sodium form (5 %) incubated overnight at 56°C, and the enzyme was annihilated with 15 min at 100°C. DNA solution was used to genotype 14 microsatellite loci selected for the SALSEA-Merge project(Ellis et al 2011). The QIAGEN's Multiplex PCR Kit was used for PCR amplification according to the manufacturer's recommendations, using an annealing temperature of 56°C.…”
mentioning
confidence: 99%