A Novel Approach To Produce Biologically Relevant Chemical Patterns at the Nanometer Scale:  Selective Molecular Assembly Patterning Combined with Colloidal Lithography

Langmuir ◽  
2002 ◽  
Vol 18 (22) ◽  
pp. 8580-8586 ◽  
Author(s):  
Roger Michel ◽  
Ilya Reviakine ◽  
Duncan Sutherland ◽  
Christian Fokas ◽  
Gabor Csucs ◽  
...  
2009 ◽  
pp. 839-841 ◽  
Author(s):  
Maria Elena Fragalà ◽  
Cristina Satriano ◽  
Graziella Malandrino

Plant Methods ◽  
2020 ◽  
Vol 16 (1) ◽  
Author(s):  
Soumyashree Kar ◽  
Ryokei Tanaka ◽  
Lijalem Balcha Korbu ◽  
Jana Kholová ◽  
Hiroyoshi Iwata ◽  
...  

Abstract Background Restricting transpiration under high vapor pressure deficit (VPD) is a promising water-saving trait for drought adaptation. However, it is often measured under controlled conditions and at very low throughput, unsuitable for breeding. A few high-throughput phenotyping (HTP) studies exist, and have considered only maximum transpiration rate in analyzing genotypic differences in this trait. Further, no study has precisely identified the VPD breakpoints where genotypes restrict transpiration under natural conditions. Therefore, outdoors HTP data (15 min frequency) of a chickpea population were used to automate the generation of smooth transpiration profiles, extract informative features of the transpiration response to VPD for optimal genotypic discretization, identify VPD breakpoints, and compare genotypes. Results Fifteen biologically relevant features were extracted from the transpiration rate profiles derived from load cells data. Genotypes were clustered (C1, C2, C3) and 6 most important features (with heritability > 0.5) were selected using unsupervised Random Forest. All the wild relatives were found in C1, while C2 and C3 mostly comprised high TE and low TE lines, respectively. Assessment of the distinct p-value groups within each selected feature revealed highest genotypic variation for the feature representing transpiration response to high VPD condition. Sensitivity analysis on a multi-output neural network model (with R of 0.931, 0.944, 0.953 for C1, C2, C3, respectively) found C1 with the highest water saving ability, that restricted transpiration at relatively low VPD levels, 56% (i.e. 3.52 kPa) or 62% (i.e. 3.90 kPa), depending whether the influence of other environmental variables was minimum or maximum. Also, VPD appeared to have the most striking influence on the transpiration response independently of other environment variable, whereas light, temperature, and relative humidity alone had little/no effect. Conclusion Through this study, we present a novel approach to identifying genotypes with drought-tolerance potential, which overcomes the challenges in HTP of the water-saving trait. The six selected features served as proxy phenotypes for reliable genotypic discretization. The wild chickpeas were found to limit water-loss faster than the water-profligate cultivated ones. Such an analytic approach can be directly used for prescriptive breeding applications, applied to other traits, and help expedite maximized information extraction from HTP data.


2021 ◽  
Vol 17 (9) ◽  
pp. e1009305
Author(s):  
Suraj Kannan ◽  
Michael Farid ◽  
Brian L. Lin ◽  
Matthew Miyamoto ◽  
Chulan Kwon

The immaturity of pluripotent stem cell (PSC)-derived tissues has emerged as a universal problem for their biomedical applications. While efforts have been made to generate adult-like cells from PSCs, direct benchmarking of PSC-derived tissues against in vivo development has not been established. Thus, maturation status is often assessed on an ad-hoc basis. Single cell RNA-sequencing (scRNA-seq) offers a promising solution, though cross-study comparison is limited by dataset-specific batch effects. Here, we developed a novel approach to quantify PSC-derived cardiomyocyte (CM) maturation through transcriptomic entropy. Transcriptomic entropy is robust across datasets regardless of differences in isolation protocols, library preparation, and other potential batch effects. With this new model, we analyzed over 45 scRNA-seq datasets and over 52,000 CMs, and established a cross-study, cross-species CM maturation reference. This reference enabled us to directly compare PSC-CMs with the in vivo developmental trajectory and thereby to quantify PSC-CM maturation status. We further found that our entropy-based approach can be used for other cell types, including pancreatic beta cells and hepatocytes. Our study presents a biologically relevant and interpretable metric for quantifying PSC-derived tissue maturation, and is extensible to numerous tissue engineering contexts.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
C. W. Woodall ◽  
A. R. Weiskittel

AbstractTree size-density dynamics can inform key trends in forest productivity along with opportunities to increase ecosystem resiliency. Here, we employ a novel approach to estimate the relative density (RD, range 0–1) of any given forest based on its current size-density relationship compared to a hypothetical maximum using the coterminous US national forest inventory between 1999 and 2020. The analysis suggests a static forest land area in the US with less tree abundance but greatly increased timber volume and tree biomass. Coupled with these resource trends, an increase in RD was identified with 90% of US forest land now reaching a biologically-relevant threshold of canopy closure and/or self-thinning induced mortality (RD > 0.3), particularly in areas prone to future drought conditions (e.g., West Coast). Notably, the area of high RD stands (RD > 0.6) has quintupled over the past 20 years while the least stocked stands (RD < 0.3) have decreased 3%. The evidence from the coterminous US forest RD distribution suggest opportunities to increase live tree stocking in understocked stands, while using density management to address tree mortality and resilience to disturbances in increasingly dense forests.


2012 ◽  
Vol 10 (01) ◽  
pp. 1240008 ◽  
Author(s):  
Sylvia Boyd ◽  
Maryam Haghighi

We provide a computationally realistic mathematical framework for the NP-hard problem of the multichromosomal breakpoint median for linear genomes that can be used in constructing phylogenies. A novel approach is provided that can handle signed, unsigned, and partially signed cases of the multichromosomal breakpoint median problem. Our method provides an avenue for incorporating biological assumptions (whenever available) such as the number of chromosomes in the ancestor, and thus it can be tailored to obtain a more biologically relevant picture of the median. We demonstrate the usefulness of our method by performing an empirical study on both simulated and real data with a comparison to other methods.


2015 ◽  
Vol 61 (5) ◽  
pp. 760-768 ◽  
Author(s):  
Lars Mørkrid ◽  
Alexander D Rowe ◽  
Katja B P Elgstoen ◽  
Jess H Olesen ◽  
George Ruijter ◽  
...  

Abstract BACKGROUND Urinary concentrations of creatine and guanidinoacetic acid divided by creatinine are informative markers for cerebral creatine deficiency syndromes (CDSs). The renal excretion of these substances varies substantially with age and sex, challenging the sensitivity and specificity of postanalytical interpretation. METHODS Results from 155 patients with CDS and 12 507 reference individuals were contributed by 5 diagnostic laboratories. They were binned into 104 adjacent age intervals and renormalized with Box–Cox transforms (Ξ). Estimates for central tendency (μ) and dispersion (σ) of Ξ were obtained for each bin. Polynomial regression analysis was used to establish the age dependence of both μ[log(age)] and σ[log(age)]. The regression residuals were then calculated as z-scores = {Ξ − μ[log(age)]}/σ[log(age)]. The process was iterated until all z-scores outside Tukey fences ±3.372 were identified and removed. Continuous percentile charts were then calculated and plotted by retransformation. RESULTS Statistically significant and biologically relevant subgroups of z-scores were identified. Significantly higher marker values were seen in females than males, necessitating separate reference intervals in both adolescents and adults. Comparison between our reconstructed reference percentiles and current standard age-matched reference intervals highlights an underlying risk of false-positive and false-negative events at certain ages. CONCLUSIONS Disease markers depending strongly on covariates such as age and sex require large numbers of reference individuals to establish peripheral percentiles with sufficient precision. This is feasible only through collaborative data sharing and the use of appropriate statistical methods. Broad application of this approach can be implemented through freely available Web-based software.


2020 ◽  
Vol 8 (48) ◽  
pp. 26035-26044
Author(s):  
Ahmad Esmaielzadeh Kandjani ◽  
Ylias M. Sabri ◽  
Victoria E. Coyle ◽  
Christopher J. Harrison ◽  
Dilek Korcoban ◽  
...  

We present a novel approach for fabricating multicomponent ordered nanostructures using colloidal lithography and electrodeposition techniques, enabling maskless, targeted and uniform material deposition.


2020 ◽  
Author(s):  
James A. Diao ◽  
Wan Fung Chui ◽  
Jason K. Wang ◽  
Richard N. Mitchell ◽  
Sudha K. Rao ◽  
...  

While computational methods have made substantial progress in improving the accuracy and throughput of pathology workflows for diagnostic, prognostic, and genomic prediction, lack of interpretability remains a significant barrier to clinical integration. In this study, we present a novel approach for predicting clinically-relevant molecular phenotypes from histopathology whole-slide images (WSIs) using human-interpretable image features (HIFs). Our method leverages >1.6 million annotations from board-certified pathologists across >5,700 WSIs to train deep learning models for high-resolution tissue classification and cell detection across entire WSIs in five cancer types. Combining cell- and tissue-type models enables computation of 607 HIFs that comprehensively capture specific and biologically-relevant characteristics of multiple tumors. We demonstrate that these HIFs correlate with well-known markers of the tumor microenvironment (TME) and can predict diverse molecular signatures, including immune checkpoint protein expression and homologous recombination deficiency (HRD). Our HIF-based approach provides a novel, quantitative, and interpretable window into the composition and spatial architecture of the TME.


2008 ◽  
Vol 07 (01) ◽  
pp. 73-79 ◽  
Author(s):  
DAE-GEUN CHOI ◽  
JUN-HO JEONG ◽  
EUNG-SUG LEE

In this work, various 2D nano- and micropatterns with the feature resolution from micrometer to nanometer scale by using colloidal self-assembly and nanoimprint lithography (or micromolding) for the fabrication of patterned catalyst pattern are fabricated. To control size and shape of colloidal templates and patterned catalyst metals, colloidal self-assembly based on bottom-up approach and dry etching conditions were deliberately controlled.


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