2020 ◽  
Vol 48 (W1) ◽  
pp. W72-W76 ◽  
Author(s):  
Vadim M Gumerov ◽  
Igor B Zhulin

Abstract Key steps in a computational study of protein function involve analysis of (i) relationships between homologous proteins, (ii) protein domain architecture and (iii) gene neighborhoods the corresponding proteins are encoded in. Each of these steps requires a separate computational task and sets of tools. Currently in order to relate protein features and gene neighborhoods information to phylogeny, researchers need to prepare all the necessary data and combine them by hand, which is time-consuming and error-prone. Here, we present a new platform, TREND (tree-based exploration of neighborhoods and domains), which can perform all the necessary steps in automated fashion and put the derived information into phylogenomic context, thus making evolutionary based protein function analysis more efficient. A rich set of adjustable components allows a user to run the computational steps specific to his task. TREND is freely available at http://trend.zhulinlab.org.


2017 ◽  
Vol 15 (6) ◽  
pp. 361-370 ◽  
Author(s):  
Soheil Jahangiri-Tazehkand ◽  
Limsoon Wong ◽  
Changiz Eslahchi

2012 ◽  
Vol 13 (1) ◽  
Author(s):  
Danielle G Lemay ◽  
William F Martin ◽  
Angie S Hinrichs ◽  
Monique Rijnkels ◽  
J Bruce German ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Rida Assaf ◽  
Fangfang Xia ◽  
Rick Stevens

AbstractContiguous genes in prokaryotes are often arranged into operons. Detecting operons plays a critical role in inferring gene functionality and regulatory networks. Human experts annotate operons by visually inspecting gene neighborhoods across pileups of related genomes. These visual representations capture the inter-genic distance, strand direction, gene size, functional relatedness, and gene neighborhood conservation, which are the most prominent operon features mentioned in the literature. By studying these features, an expert can then decide whether a genomic region is part of an operon. We propose a deep learning based method named Operon Hunter that uses visual representations of genomic fragments to make operon predictions. Using transfer learning and data augmentation techniques facilitates leveraging the powerful neural networks trained on image datasets by re-training them on a more limited dataset of extensively validated operons. Our method outperforms the previously reported state-of-the-art tools, especially when it comes to predicting full operons and their boundaries accurately. Furthermore, our approach makes it possible to visually identify the features influencing the network’s decisions to be subsequently cross-checked by human experts.


Agronomy ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 2587
Author(s):  
Oliver Schliebs ◽  
Chon-Kit Kenneth Chan ◽  
Philipp E. Bayer ◽  
Jakob Petereit ◽  
Ajit Singh ◽  
...  

Daisychain is an interactive graph visualisation and search tool for custom-built gene homology databases. The main goal of Daisychain is to allow researchers working with specific genes to identify homologs in other annotation releases. The gene-centric representation includes local gene neighborhood to distinguish orthologs and paralogs by local synteny. The software supports genome sequences in FASTA format and GFF3 formatted annotation files, and the process of building the homology database requires a minimum amount of user interaction. Daisychain includes an integrated web viewer that can be used for both data analysis and data publishing. The web interface extends KnetMaps.js and is based on JavaScript.


2017 ◽  
Vol 18 (1) ◽  
Author(s):  
Se-Ran Jun ◽  
Intawat Nookaew ◽  
Loren Hauser ◽  
Andrey Gorin

2014 ◽  
Vol 26 (4pt1) ◽  
pp. 1113-1128 ◽  
Author(s):  
Man-Kit Lei ◽  
Ronald L. Simons ◽  
Mary Bond Edmond ◽  
Leslie Gordon Simons ◽  
Carolyn E. Cutrona

AbstractSocial disorganization theory posits that individuals who live in disadvantaged neighborhoods are more likely to engage in antisocial behavior than are those who live in advantaged neighborhoods and that neighborhood disadvantage asserts this effect through its disruptive impact on social ties. Past research on this framework has been limited in two respects. First, most studies have concentrated on adolescent males. In contrast, the present study focused on a sample of adult African American females. Second, past research has largely ignored individual-level factors that might explain why people who grow up in disadvantaged neighborhoods often do not engage in antisocial behavior. We investigated the extent to which genetic variation contributes to heterogeneity of response to neighborhood conditions. We found that the impact of neighborhood disadvantage on antisocial behavior was mediated by neighborhood social ties. Further, the analysis indicated that the effects of neighborhood disadvantage and social ties on antisocial behavior were moderated by genetic polymorphisms. Examination of these moderating effects provided support for the differential susceptibility model of Gene × Environment. The effect of Gene × Neighborhood Disadvantage on antisocial behavior was mediated by the effect of Gene × Neighborhood Social Ties, providing support for an expanded view of social disorganization theory.


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