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LNJC authored Oct 11, 2023
2 parents 642a768 + 3b86d72 commit 9097476
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2 changes: 1 addition & 1 deletion .github/workflows/build.yml
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Expand Up @@ -34,7 +34,7 @@ jobs:
run: pnpm install

- name: Build site
run: npm run build -- --prefix-paths --verbose --no-color
run: npm run build -- --verbose --no-color

- name: Send bundle stats to RelativeCI
uses: relative-ci/agent-action@v2
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10 changes: 5 additions & 5 deletions package.json
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"dependencies": {
"@emotion/react": "^11.11.1",
"@emotion/styled": "^11.11.0",
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"katex": "^0.16.9",
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"gatsby-transformer-yaml": "^5.12.0",
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2 changes: 1 addition & 1 deletion pages/mdx/description.mdx
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Expand Up @@ -24,4 +24,4 @@ It is being shipped via appimages and ships with a beta version of NUPACK that w

The final objective was to raise awareness about women's health and the specific illnesses that are related to it. These conditions are largely unknown while being common and frequently have a negative impact on lives in both developed and developing countries. We have carefully considered how our sensor might be applied in a clinical environment as a component of our work in human practises. As part of our integrated human practises, we spoke with numerous clinicians and established a plan for how our test might be utilised in screening programmes. On their advice, we have also increased our sensor's sensitivity and specificity. We have also looked into the potential detection of other diseases by our sensor and the advantages of our approach.

In a clinical implementation, miRNAs extracted from blood serum would be added to a cell free system containing an excess of our amalgamation. The unique toehold switches would detect specific miRNAs and regulate translation of the corresponding fluorescent protein in response. The intensity of fluorescence produced by our circuits is therefore indicative of the miRNA levels in the body fluid. To help reduce costs, we designed and built a £4 combined fluorometer and densitometer, coined a luminometer, to cheaply quantify the fluorescence from our circuit without a plate reader. This allows our test to be used in the field and in less developed countries.
In a clinical implementation, miRNAs extracted from blood serum would be added to a cell free system containing an excess of our amalgamation. The unique toehold switches would detect specific miRNAs and regulate translation of the corresponding fluorescent protein in response. The intensity of fluorescence produced by our circuits is therefore indicative of the miRNA levels in the body fluid. To help reduce costs, we designed and built a £4 combined fluorometer and densitometer, coined a luminometer, to cheaply quantify the fluorescence from our circuit without a plate reader. This allows our test to be used in the field and in less developed countries.
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