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To construct a suitably robust map, we followed the strategy described by Yang et al. [ 55].
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To bring the atomic structure into registration with the volumetric map, we follow a three-step procedure (Fig. 1).
To extract feature points from a density map we follow a procedure by Wriggers et al. (1999) and adopt a fast VQ technique based on the neural gas clustering technique.
In addition to the established binary measure for the co-occurrence of genes on the same KEGG PATHWAY map, we follow a more recent suggestion [ 14] that utilizes the annotation graphs defined by the Gene Ontology (GO) consortium.
As results were inconclusive when the male sterility character was mapped as a single gene in the T×E, T1E, and E maps, we followed a two-step procedure.
For mapping, we followed the strategy of "selective" or "bin" mapping [ 26, 37] where, based on the data of a detailed map already constructed (in this case the TxE map), a few plants are selected having a high number of recombination breakpoints and an approximately even distribution of these breakpoints throughout the genome.
For genetic map construction, we followed the two-way pseudo-test cross approach [ 38].
To make every unique small RNA map to only one annotation, we followed the following priority rule: rRNAetc(in which Genbank > Rfam) > known miRNA > repeat > exon > intron.
To make every unique small RNAs mapped to only one annotation, we followed the following priority rule: rRNAetc (Genbank > Rfam) > known miRNA > repeat > exon > intron [ 33].
Air Vice Marshal S Nair, a senior air force officer, traces our route on a map as we follow the Ganges river.
That is the political road map we must follow to victory.
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