Exome sequence variants were identified using a modified version of the 1000 Genomes Project variant calling pipeline (1000 Genomes Project Consortium, 2010; Kettleborough et al., 2013).
Using a modified version of the 1000 Genomes Project variant calling pipeline, we first identified homozygous genomic differences between the male and female in each cross (1000 Genomes Project Consortium, 2010; Kettleborough et al., 2013).
Copy-number variants were detected using a modified version of CNAseq developed at the Michael Smith Genome Sciences Centre, as described (Shah et al. 2006; Jones et al. 2010).
We used a modified version of gibsonsec's exploit/method.
The results obtained by the proposed MOPSO algorithm were compared with those obtained using a modified time-variant MOPSO, the non-dominated sorting genetic algorithm, strength Pareto evolutionary algorithm, and the exact solution method where possible.
The solubility values were fitted using a modified Apelblat model, a variant of the combined nearly ideal binary solvent/Redich-Kister (CNIBS/R-K) model and Jouyban-Acree model in (tetrahydrofuran + acetonitrile) binary solvent mixture.
The solubility data were fitted using a modified Apelblat model, a variant of the combined nearly ideal binary solvent/Redich-Kister (CNIBS/R-K) model, Jouyban-Acree model and Ma model in (1-butanol + acetonitrile) binary solvent mixture.
Also, a modified variant of the approach, based on auto-generated machine code is presented.
Even in this case, however, the recombinant TRPV1 variant (produced using a modified baculovirus system) was composed of amino acids 110 603 and 627 764, demonstrating the importance of prior biochemical characterisation [ 10].
More recently, Uauy et al. [ 19] using a modified TILLING approaches detected novel allelic variants of SBEIIa and SBEIIb genes in tetraploid and hexaploid wheats.
