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Secondary structural predictions were initially made using HHpred program and generally predicted two anti-parallel helices per PPR [ 47].
Combining the three refinement steps, 1262 out of 1412 predictions were initially consistent with experimental results.
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SNP prediction was initially performed using MAQ mapping and assembly software [ 26].
Consequently, application of information entropy to B-cell epitope prediction was initially outlined in preliminary form [ 56] and much more extensively elaborated in the present work vis-a-vis the body of pertinent data currently available via IEDB, within the practically meaningful context of prospective biomedical applications with due emphasis on pharmaceutical product development.
Out of 1412 predictions, 1262 were initially consistent with our experimental observations.
Prediction models were initially generated using ANNE and RF.
For the GP prediction model, populations of 3000 individuals were initially evolved and arithmetic functions: add, minus, protected division and product were defined as the function set [ 10].
Multiple methods were initially tested for SNP prediction and filtering.
Based on standard computational prediction, together with experimental data, 4,824 genes and 31 pseudogenes were initially annotated.
Doctors were initially mystified.
Romanians were initially popular.
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