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Contigs with significant alignment were selected for further analysis.
The proteins indicated in alignment were selected for the next step of the analysis.
Conserved regions in the alignment were selected to infer the transposase phylogeny.
The alignments that produced phylogeny incongruent with that predicted based on concatenated alignment were selected as representing a single recombination event.
The protein sequences for this alignment were selected based on their similarity (E value < -20) with SP212 using the BLASTx tool.
To benchmark the SNP identification method, 163 SNPs, in which the polymorphism was represented twice in the sequence alignment, were selected and tested on a panel of three purebred boar lines and wild boar.
Similar(53)
If a sequence read aligned to more than one genomic locus, the best alignment was selected.
An ungapped segment of the alignment was selected to be the artificially misaligned segment.
The longest alignment was selected for analysis.
If alignment length is identical then the highest confidence alignment is selected.
For the means in Table 2, multiple alignment was selected directly and the results automatically recorded.
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