Sentence examples for design transcripts from inspiring English sources

This approach is explained on a theoretical level and illustrated with examples drawn from design transcripts.

With this experimental design, transcript variation can be decomposed into within-mouse and between-mouse variance components.

Primer Express 3 software (Applied Biosystems) was used to design transcript-specific primers to amplify up to 100-bp regions of all genes of interest.

Due to the overall difference in platform design, transcript level estimation, and gene annotation, direct comparisons are difficult and only a few attempts have been made to compare these different platforms.

The translational efficiencies of the designed transcripts were 0.49 for DsRed2-H and 0.072 for DsRed2-L.

To validate some of these new transcripts, we designed transcript-specific primers, extracted total RNA from ovaries and were able to reliably produce RT-PCR products from seven of ten haphazardly selected novel candidates.

The participant sex breakdown reflected the institution's ratio of 59% female; as age, gender, and ethnicity were not targeted in our research design, the transcripts reflect this de-identification.

The approach, without a specific design, generates transcripts with slight variations in intergenic regions that change RNAase cleavage sites, ribosomal binding sites sequestering sequences and mRNA secondary structures.

In brief, primers were designed for transcripts using Real Time PCR Primer Design tool (http://www.genscript.com/cgi-bin/tools/primer∠_genscript.cgi op=standard).

We thank Dr. K.V. Dmytruk for design of transcript analysis experiment and edition of manuscript.

Primer Express software (version 2.0) was used for the primer-probe design with transcript sequences from the NetAffx website.