https://en.wikipedia.org/wiki/Canonical_correlation#Hypothesis_testing
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https://en.wikipedia.org/wiki/Canonical_correlation#Hypothesis_testing
https://www.glowscript.org/#/user/mayalew/folder/MyPrograms/program/EpiModeling/edit
https://www.software.ac.uk/which-journals-should-i-publish-my-software
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| This mutation is of particular concern, because it occurs at a conservative domain of the receptor binding domain (RBD) directly involved in ACE2 binding. Results from some preliminary studies suggest the Y453F mutation affects the ability of the Spike protein to bind with ACE2, while others demonstrate that the mutated spike can escape from detection from a commercial anti-S antibody. | ||
| Although there is still no clear evidence indicating this mutation, or any other mutation like the popular D614G, has any clinical significance, the characteristics of the mutations need to be thoroughly investigated in the context of vaccine and antibody therapy. | ||
| Sino Biological has launched the recombinant Y453F RBD protein. This product is the newest addition to a large library of recombinant spike variants (full list here). These proteins can be used to evaluate the efficacy of the antibodies and vaccination. | ||
| Full List of SARS-CoV-2 Spike Mutants | ||
Daniel B. Forger.
https://www.ncbi.nlm.nih.gov/books/NBK544607/
https://www.ncbi.nlm.nih.gov/books/NBK544607/pdf/Bookshelf_NBK544607.pdf
Forger said that many bio clock use the same mathematic equations (models). convergent evolution. Forger said that Hoff bifurcation seems to be the common cause in all biological clocks.
J Tyson seems to have strong reservation on Forger's argument of evolution of the general math equation.
General structure of clocks.
not all bacteria has circadian clocks.
Inclusive model of expression dynamics with metabolic labeling based scRNA-seq / multiomics, vector field reconstruction and potential landscape mapping.
https://github.com/aristoteleo/dynamo-release
Li, ..., Barabasi, Science, 2017,
temporal network advantages.27. J. Wang, X. Peng, M. Li, Y. Pan, Construction and application of dynamic protein interaction
network based on time course gene expression data. Proteomics 13, 301–312 (2013).
doi:10.1002/pmic.201200277 Medline
In Figure S6, a digram is presented to describe the construct of a yeast dynamic PPI. An interaction is consider as active when both protein are active at that time point. based on X. Tang, J. Wang, B. Liu, M. Li, G. Chen, Y. Pan, A comparison of the functional modules identified from time course and static PPI network data. BMC Bioinformatics 12, 339
(2011). doi:10.1186/1471-2105-12-339 Medline
https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-12-339#Sec17
In Fig 2. Protein networks used contain only 84, 74, and 85 nodes. So, it seems Li17 only used a small subset of PPI.
Li17 fixed the number of driver nodes to 20% of the nodes. Hong did not find the criteria on the reasons behind this choice.
https://www.baeldung.com/cs/latex-drawing-graphs
http://genomicsclass.github.io/book/
https://github.com/genomicsclass/labs
good post to prove that geometric and algebraic multiplicity are the same for a symmetric matrix.
https://www.nature.com/articles/nsmb.2737
In budding yeast, a single double-strand break (DSB) triggers extensive Tel1 (ATM)- and Mec1 (ATR)-dependent phosphorylation of histone H2A around the DSB, to form γ-H2AX
In Saccharomyces cerevisiae, histone H2A comprises the great majority of H2A isoforms and is phosphorylated on S129; we will refer to this modification also as γ-H2AX. Both in yeast and in mammals, γ-H2AX rapidly spreads on large chromatin domain (on more than a megabase in mammals and about 50 kb in yeast)
Both γ-H2AX and γ-H2B are strongly diminished over highly transcribed regions.
https://en.wikipedia.org/wiki/Coding_theory
this is related to encryption and error detection.
Is this related to how DNA use quaternary code and basepairing?