Saturday, December 19, 2020

Ayalew SIR model script

 

https://www.glowscript.org/#/user/mayalew/folder/MyPrograms/program/EpiModeling/edit



Wednesday, December 16, 2020

proteostasis collapase is a driver of cell aging and death

 Santra, Deill, and de Graff, PNAS 2019

use folded and unfoled protein, damage to model aging. 




 

Tuesday, December 15, 2020

Monday, December 14, 2020

sino biolgical, List of SARS-CoV-2 Spike Mutants

 

An unprecedented mink cull has been ordered in Denmark amid the outbreak of SARS-CoV-2 in these farmed animals. The plan was announced after scientists discovered a widespread Y453F mutation in the spike protein, that has been passed from animal to humans. animal
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
P337S F338L V341I F342L A344S
 
A348S N354D A352S S359N V367F
 
N370S A372T A372S F377L K378N
 
K378R P384L T385A T393P V395I
 
E406Q R408I Q409E Q414R Q414E
 
K417N A435S W436R N439K N440K
 
K444R V445F G446V G446S L452R
 
Y453F F456L F456E K458R K458Q
 
E471Q I472V G476S S477R S477I
 
S477N T478I P479S N481D G482S
 
V483A V483I G485S F486S F490S
 
S494P P499R V503F Y505C Y508H
 
A520V A520S P521S P521R A522V
 
A522S D614G D405V, Q414A

Friday, December 11, 2020

biological clocks, Forger,

Biological Clocks, Rhythms, and Oscillations

The Theory of Biological Timekeeping

.

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. 



Dynamo: Mapping Vector Field of Single Cells

 

Dynamo: Mapping Vector Field of Single Cells

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



linear dynamic systems, laplace transform

 

https://see.stanford.edu/Course/EE263 

https://see.stanford.edu/materials/lsoeldsee263/13-lin-sys.pdf


Thursday, December 10, 2020

advantages of temporal network, continued

 Li, ..., Barabasi, Science, 2017,

temporal network advantages.

Energy needed from state vector x0 to final state xf
  E(x0, xf) = 1/2 d^T x W^01_eff  x d

where Weff encode the energy structure of the network.

I did not follow S1.1 method. 

After reading Laplace transformation, and watched YouTube movies on solving differential equations with Laplace transformation, it seems the Li17 presented a general solution. 

Li17 cited a yeast dynamic protein network: 

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. 











draw a graph diagram on latex

 

https://www.baeldung.com/cs/latex-drawing-graphs


Tuesday, December 8, 2020

PH525x series - Biomedical Data Science

 

http://genomicsclass.github.io/book/

https://github.com/genomicsclass/labs


geometric multiplicity == algebraic multiplicity-for-a-symmetric-matrix

 good post to prove that geometric and algebraic multiplicity are the same for a symmetric matrix.

https://math.stackexchange.com/questions/393149/geometric-multiplicity-algebraic-multiplicity-for-a-symmetric-matrix





yeast double strand breaks, γ-H2AX and γ-H2B

 

Dynamics of yeast histone H2A and H2B phosphorylation in response to a double-strand break

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.


coding theory

 

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?