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To facilitate comparative genomic analyses, we devised a simple method for the development of microsatellite markers at target chromosomes and genomic regions using the sequenced genomes of other species.
To facilitate the comparative genomic analyses, we devised a simple method for the development of microsatellite markers for target chromosomes and genomic regions in nine-spined sticklebacks using the sequenced genomes of other fish species.
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To analyse the data, we devised a CNV detection strategy based on Poisson-Gamma and Poisson-Lognormal, two probability distributions known for their flexibility in tackling overdispersion.
To try to overcome this limitation, we devised a Severity Score (Table 5) to use in our analyses.
We devised a systematic review protocol according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
We devised a system to transform data from the RIG task, which is continuous, to be analysed with RGCalc software 3, as suggested by Towse and Neil (1998).
To capture a sample of studies that involved PD analyses and invasive tissue procurement while excluding the very large volume of studies involving minimally invasive collection (for example, venipuncture), we devised a search strategy that was highly specific.
We devised a direct assay for cardiac specification to facilitate identification of cardiac-inducing signal(s) and in-depth analyses of the process.
To change that, we devised a little experiment.
We devised a permutation test to evaluate this possibility.
In this study, we devised a two-stage mapping protocol.
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