v0.5.10
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cDNA replaces qPCR throughout (when referring to cDNA gene expression style assays). qPCR didn't make sense, as gDNA primers can be used in qPCR.
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contig argument is removed from primary functions, instead users should supply a contig:position string as the target. for example
2L:28545767
. For cDNA primers, target should be an AGAP identifier, from which the contig will be automatically determined. -
In the long notebook, there is now a single prepare_sequence function instead of two functions with an if else statement.