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Hi team,
I am Rosti Readioff, I am currently a research fellow at Leeds University on an EPSRC funded knee programme. I am working on developing specimen-specific pathological knee joint models in…
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I posted a blog post today with my reflections about what to do with the high frequency content of an acceleration signal: https://accelting.com/updates/high-frequencies-in-an-acceleration-signal/
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Hi all,
I used a dummy enzyme which only expressed in the `liver` and adjusted the` in vitro specific clearance` to see what happens. However, in an IV simulation I found the `total body clearance`…
jzq90 updated
3 years ago
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**Abstract**:
In the setting of predicting the status of AD. I demonstrated that Polygenic Univariate TWAS fail to capture satisfaction amount of information from multiple tissues data, revealed that…
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> Task Group will make a recommendation [...] as to which class in the Darwin Core standard these properties belong which may also include recommendations for terms being revised, added, disambiguated…
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Here are two papers, one on protein therapeutics and one review. I am currently reading two additional papers; one to do with cell lysis through quorum sensing and one which is talking about automatio…
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Hi,
The pipeline has been working very well! However, I am running on mouse data and saw that there is a note about a mouse nuclei UnMicst model in the documentation
> --model
> The name of the U…
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**Submitting author:** @glyg (Guillaume Gay)
**Repository:** https://github.com/damcb/tyssue
**Version:** 0.9.0
**Editor:** @pdebuyl
**Reviewer:** @fcooper8472, @SergeDmi
**Archive:** 10.5281/zenodo.4…
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I am using GECKO to obtain the enzyme constraint HumanGEM model but most of the files are written for the saccharomyces cerevisiae model. I am having problems with adapting the toolbox to HumanGEM.
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## FEATURE DESCRIPTION
### Feature Inspiration
We need a way to track the provenance of imported PeakGroup data, both for error checking and later lookup. Also, there is potentially some value…