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The trimmed protein alignments were subsequently reverse translated into nucleotide alignments using the original sequences.
The aa alignments were then used as a template for creating nucleotide sequence alignments using the original, untranslated sequences.
These were obtained by randomizing the ASTRAL subset sequences using the original amino acid frequencies.
DNA sequences of the PCR amplicons were determined from both forward and reverse sequence data using the original primer pairs.
This way, objective quality measurements could be done, using the original sequences progressive frames as references.
This time, using the original feather color.
Remodeling of the original sequences using α-helix-inducible motifs revealed the interactive residues of gp40.
To keep the solution space continuous, we restructured the original sequences using a sequence mapping.
Sequences were compared to the original sequences used for the inoculum.
The production team used the original script, surviving sequence storyboards, memos, and the director's recollections.
After removing the vector and primer sequences, CLUSTAL_X [ 36] was used to compare the DNA sequences of the two parents and the original sequences.
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