Genotyping was carried out at the Gifu University, and genotypic data were arranged, validated and stored in the MAPGENA database.
These population data were arranged into sibships and mother-offspring units through unique personal numbers.
After data acquisition, PET data were arranged into sinograms and subsequently reconstructed with the maximum a posteriori (MAP) reconstruction algorithm.
PET data were arranged into sinograms and subsequently reconstructed with the maximum a posteriori (MAP) reconstruction algorithm.
The BLAST data were arranged in maximum percentage identity and first ten sequences was selected and exported in FASTA format.
Themes were refined through the indexing process and chunks of data were arranged according to the refined thematic labels and charted within a matrix against the unique identifier used for each participant.
All the experimental data were arranged in Microsoft Excel spreadsheet and subjected to regression in Solver® program.
We work in universal time (UT), and for each altitude and latitude, the data were arranged in a matrix with 24 columns (this is the longitude with a step of 15°) and the number of rows is equal to the length of the considered period of time in hours.
Parasites were identified by genus or group and the data were arranged in prevalence by the formula: number of infected fish with parasites ÷ number of fish analyzed × 100.
The gamma camera was rotated continuously for 16 minutes, and SPECT data were arranged into 90 projections over 360°.
