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We provide a method adaptable to aquatic organisms to study the direct regulation of estrogen-responsive genes in vivo.
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While we used COI sequences, this method is adaptable to any chosen genetic marker.
The method is adaptable to all organisms (i.e., plants, animals, fungi, bacteria) and all genetic markers (i.e., COI, ITS, rbcL, 16S, 18S).
Expansion of this method is adaptable to retrieve 3′-UTRs encoded in more than one exon by removing the introns from the BAC first with recombineering.
By analyzing the instantaneous energy of single-hole blasting signal, it was found that the instantaneous energy method was adaptable to millisecond blasting with delay time longer than half of the energy peak period.
In addition, the method is adaptable to most fDOT or planar optical imaging instruments with surface reconstruction.
This method is adaptable to high throughput screening.
The new in vitro multiple stress dormancy model efficiently generates Mtb cells meeting all criteria of dormancy, and this method is adaptable to high-throughput screening for drugs that can kill dormant Mtb.
The computing method is adaptable to the analysis of a data set including pairs of GIAs with imperfect relationships.
The method is adaptable to many different lens designs and will allow a fully optically integrated device suitable for true POC and remote sensing applications.
This method is adaptable to other platforms, such as next-generation sequencing, which has recently been used to identify fetal cfDNA in maternal plasma.
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