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The SLAF markers were partitioned into LGs based on a pairwise modified logarithm of odds (MLOD) scores.
Following Hughes and Eastwood [ 16], the two markers were partitioned and analyzed under GTR+Γ and GTR+I models, respectively.
These markers were partitioned into maternal (1 : 1 female type; 2473 markers) and paternal (1 : 1 male type; 2175 markers) datasets for constructing sex-specific linkage maps.
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These markers are partitioned among a number of total orders called chromosomes.
Using these markers, F. virguliforme isolates were partitioned into three distinct clusters, but isolates were not grouped based on relatedness of sampling sites.
With these markers, the two genomes were partitioned into syntenic blocks.
Both datasets were partitioned into the number of markers used by directly editing of the XLM file and following Couvreur [ 44].
The PCR products were partitioned by electrophoresis on agrose gel with DNA markers (TaKaRa).
Because all five genetic markers are protein-coding genes, the rapidly evolving third codon positions were partitioned from the slower evolving first and second positions in Bayesian and likelihood analyses, resulting in ten total partitions [ 90].
The different locus combinations were partitioned for independent model assessment at each marker.
The number of clusters (k) was determined by allowing only the cytosolic compartment (represented by three compartment-specific markers) to be partitioned into different clusters without being assigned onto another compartment.
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