The best match was selected based on the presence of similar domains and plausibility quality control.
In this case, a match was selected at random.
The occupation that exhibited the best match was selected.
In the case of multiple matches, the best match was selected.
This first match was selected to fit our protein to a 3D model.
The top-scoring BLAST (http://blast.ncbi.nlm.nih.gov/) match was selected to identify the specific genome.
When there were more than two nonexposed patients for an exposed patient, only the nonexposed patient with the best overall match was selected.
A subset of hospital discharge records was then matched to a subset of RAC entry records and a single (if any) match was selected based on the match weight.
Briefly, the set of proteins of each biclique was compared to the known yeast complexes cataloged in MIPS, and the most significant match was selected, using a hypergeometric score.
The best BLAST matches were selected based on e-value and sequence coverage at each KOG category.
