https://pages.htgaa.org/2026b/jeffrey-richards/index.htmlAbout me This is a test of edit.htgaa.org Hello World! Contact info www.linkedin.com/in/jeffreysrichards Homework, Labs, and Projects See the nav bar on the left to look through my work for How To Biomanufacture Almost Anything (Fall 2026)!Hugoenhttps://pages.htgaa.org/2026b/jeffrey-richards/week-01-hw-project-ideas/index.htmlMon, 01 Jan 0001 00:00:00 +0000https://pages.htgaa.org/2026b/jeffrey-richards/week-01-hw-project-ideas/index.htmlGreetings…! So I kind of just stumbled on HTBAA from a post on LinkedIn. I hope to really give this a full-faith effort, but there is so much to learn and so little time. I will at first try not to rely on AI-assisted responses so that my initial thoughts and ideas are unaided. Essentially, this is a learning experience, and I want to be able to look back on this project as a time when AI was starting to ramp up. I will answer the initial questions now, sans AI, and later expand on the responses as needed. Let’s go…!https://pages.htgaa.org/2026b/jeffrey-richards/week-02-hw-dna-design/index.htmlMon, 01 Jan 0001 00:00:00 +0000https://pages.htgaa.org/2026b/jeffrey-richards/week-02-hw-dna-design/index.htmlAfter viewing the recitation from Spring 2026, it took me quite a long time to understand what was going on. However, there is a lot to say that has not really been said. First off, one has to understand what “glyphs” are in the field of syn bio (https://sbolstandard.org/visual-glyphs/). A solid example can be found at (https://sbolstandard.org/visual-examples/) where “Example 1” shows an example of a very small plasmid comprised of a: promoter, RBS, CDS, and terminator.https://pages.htgaa.org/2026b/jeffrey-richards/final-project/index.htmlMon, 01 Jan 0001 00:00:00 +0000https://pages.htgaa.org/2026b/jeffrey-richards/final-project/index.html