scholarly journals Rotation of Biological Cells: Fundamentals and Applications

Engineering ◽  
2021 ◽  
Author(s):  
Tao Tang ◽  
Yoichiroh Hosokawa ◽  
Takeshi Hayakawa ◽  
Yo Tanaka ◽  
Weihua Li ◽  
...  
Keyword(s):  
PIERS Online ◽  
2009 ◽  
Vol 5 (3) ◽  
pp. 251-255 ◽  
Author(s):  
Hsin-Hung Li ◽  
Jen-Yu Jao ◽  
Ming-Kun Chen ◽  
Ling-Sheng Jang ◽  
Yi-Chu Hsu

2019 ◽  
Vol 73 (8) ◽  
pp. 893-901
Author(s):  
Sinead J. Barton ◽  
Bryan M. Hennelly

Cosmic ray artifacts may be present in all photo-electric readout systems. In spectroscopy, they present as random unidirectional sharp spikes that distort spectra and may have an affect on post-processing, possibly affecting the results of multivariate statistical classification. A number of methods have previously been proposed to remove cosmic ray artifacts from spectra but the goal of removing the artifacts while making no other change to the underlying spectrum is challenging. One of the most successful and commonly applied methods for the removal of comic ray artifacts involves the capture of two sequential spectra that are compared in order to identify spikes. The disadvantage of this approach is that at least two recordings are necessary, which may be problematic for dynamically changing spectra, and which can reduce the signal-to-noise (S/N) ratio when compared with a single recording of equivalent duration due to the inclusion of two instances of read noise. In this paper, a cosmic ray artefact removal algorithm is proposed that works in a similar way to the double acquisition method but requires only a single capture, so long as a data set of similar spectra is available. The method employs normalized covariance in order to identify a similar spectrum in the data set, from which a direct comparison reveals the presence of cosmic ray artifacts, which are then replaced with the corresponding values from the matching spectrum. The advantage of the proposed method over the double acquisition method is investigated in the context of the S/N ratio and is applied to various data sets of Raman spectra recorded from biological cells.


2020 ◽  
Vol 128 (16) ◽  
pp. 160902 ◽  
Author(s):  
Fernando Pérez-Cota ◽  
Rafael Fuentes-Domínguez ◽  
Salvatore La Cavera ◽  
William Hardiman ◽  
Mengting Yao ◽  
...  

1990 ◽  
Vol 56 (523) ◽  
pp. 700-708
Author(s):  
Toshio FUKUDA ◽  
Osamu HASEGAWA ◽  
Hajime ASAMA ◽  
Teruyuki NAGAMUNE ◽  
Isao ENDO

2016 ◽  
Vol 27 (3) ◽  
pp. 421-423
Author(s):  
Daniel Branton

In 1961, the development of an improved freeze-etching (FE) procedure to prepare rapidly frozen biological cells or tissues for electron microscopy raised two important questions. How does a frozen cell membrane fracture? What do the extensive face views of the cell’s membranes exposed by the fracture process of FE tell us about the overall structure of biological membranes? I discovered that all frozen membranes tend to split along weakly bonded lipid bilayers. Consequently, the fracture process exposes internal membrane faces rather than either of the membrane’s two external surfaces. During etching, when ice is allowed to sublime after fracturing, limited regions of the actual membrane surfaces are revealed. Examination of the fractured faces and etched surfaces provided strong evidence that biological membranes are organized as lipid bilayers with some proteins on the surface and other proteins extending through the bilayer. Membrane splitting made it possible for electron microscopy to show the relative proportion of a membrane’s area that exists in either of these two organizational modes.


Sign in / Sign up

Export Citation Format

Share Document