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Fig. 1 Genome-wide analysis of ASE in F1 at (left) non- and (right) water-stress conditions (for 2× fold minimum expression).

Color bar represents scale for log2 fold change in expression.

Color bar at the bottom represents scale for log2 fold change in expression.

For log2 fold changes >0.00001 the values >81.25th percentile were defined as up-regulated and for log2 fold changes <−0.00001 the values <18.75th percentile were defined as down-regulated.

For example, phosphatase (PP) 2C was induced for about 4 – fold in CS1h, but for more than 16 – fold in TAM1h, while another protein phosphatase was induced for more than 32 – fold in CS1h, but for 4 – fold in TAM1h.

The last column indicates standard errors +/- SEM for log2 fold changes.

The largest enrichments were found for non-synonymous SNPs, ranging for 4 fold to 32 fold, depending on the trait.

The charge density curves were found generally to diverge with increasing pH, with the difference in charge density ranging from 0.01 to 0.43 meq/g at pH 5.0 for 2-fold increase in ionic strength.

Cross-validation tests were carried out for 20 folds.

Costs ranged from $8,005 for 87-fold coverage of one genome because genomes are sequenced in fragments of DNA, they must be sequenced multiple times to correctly assemble those fragments to $1,726 for 45-fold coverage of Church's genome.

Meanwhile, type I procollagen produced by hBMSC was increased for 3.02-fold after 2 weeks culture.