scholarly journals CLAST: CUDA implemented large-scale alignment search tool

2014 ◽  
Vol 15 (1) ◽  
Author(s):  
Masahiro Yano ◽  
Hiroshi Mori ◽  
Yutaka Akiyama ◽  
Takuji Yamada ◽  
Ken Kurokawa
Soft Matter ◽  
2006 ◽  
Vol 2 (12) ◽  
pp. 1089-1094 ◽  
Author(s):  
Violetta Olszowka ◽  
Markus Hund ◽  
Volker Kuntermann ◽  
Sabine Scherdel ◽  
Larisa Tsarkova ◽  
...  

Pramana ◽  
2004 ◽  
Vol 62 (3) ◽  
pp. 679-682
Author(s):  
Pankaj Jain ◽  
Sukanta Panda ◽  
S. Sarala

2021 ◽  
Author(s):  
Cameron LM Gilchrist ◽  
Yit Heng Chooi

Abstract Background: Fungi are prolific producers of secondary metabolites (SMs), which are bioactive small molecules with important applications in medicine, agriculture and other industries. The backbones of a large proportion of fungal SMs are generated through the action of large, multi-domain megasynth(et)ases such as polyketide synthases (PKSs) and nonribosomal peptide synthetases (NRPSs). The structure of these backbones is determined by the domain architecture of the corresponding megasynth(et)ase, and thus accurate annotation and classification of these architectures is an important step in linking SMs to their biosynthetic origins in the genome. Results: Here we report synthaser, a Python package leveraging the NCBI's conserved domain search tool for remote prediction and classification of fungal megasynth(et)ase domain architectures. synthaser is capable of batch sequence analysis, and produces rich textual output and interactive visualisations which allow for quick assessment of the megasynth(et)ase diversity of a fungal genome. synthaser uses a hierarchical rule-based classification system, which can be extensively customised by the user through a web application (http://gamcil.github.io/synthaser). We show that synthaser provides more accurate domain architecture predictions than comparable tools which rely on curated profile hidden Markov model (pHMM)-based approaches; the utilisation of the NCBI conserved domain database also allows for significantly greater flexibility compared to pHMM approaches. In addition, we demonstrate how synthaser can be applied to large scale genome mining pipelines through the construction of an Aspergillus PKS similarity network. Conclusions: synthaser is an easy to use tool that represents a significant upgrade to previous domain architecture analysis tools. synthaser is freely available under a MIT license from PyPI (https://pypi.org/project/synthaser) and GitHub (https://github.com/gamcil/synthaser). Keywords: secondary metabolism, domain architecture, polyketide synthase, nonribosomal peptide synthetase, bioinformatics, software


1986 ◽  
Vol 91 ◽  
pp. 471 ◽  
Author(s):  
P. C. Argyres ◽  
E. J. Groth ◽  
P. J. E. Peebles ◽  
M. F. Struble

2013 ◽  
Vol 770 (1) ◽  
pp. L12 ◽  
Author(s):  
Cheng Li ◽  
Y. P. Jing ◽  
A. Faltenbacher ◽  
Jie Wang

ACS Nano ◽  
2013 ◽  
Vol 7 (10) ◽  
pp. 8385-8396 ◽  
Author(s):  
Xingjie Zan ◽  
Sheng Feng ◽  
Elizabeth Balizan ◽  
Yuan Lin ◽  
Qian Wang

2021 ◽  
Vol 503 (2) ◽  
pp. 2665-2675
Author(s):  
Michael L Katz ◽  
Olivia R Cooper ◽  
Michael W Coughlin ◽  
Kevin B Burdge ◽  
Katelyn Breivik ◽  
...  

ABSTRACT Many inspiraling and merging stellar remnants emit both gravitational and electromagnetic radiation as they orbit or collide. These gravitational wave events together with their associated electromagnetic counterparts provide insight about the nature of the merger, allowing us to further constrain properties of the binary. With the future launch of the Laser Interferometer Space Antenna (LISA), follow-up observations and models are needed of ultracompact binary (UCB) systems. Current and upcoming long baseline time domain surveys will observe many of these UCBs. We present a new fast periodic object search tool capable of searching for generic periodic signals based on the conditional entropy algorithm. This new implementation allows for a grid search over both the period (P) and the time derivative of the period ($\dot{P}$). To demonstrate the usage of this tool, we use a small, hand-picked subset of a UCB population generated from the population synthesis code cosmic , as well as a custom catalogue for varying periods at fixed intrinsic parameters. We simulate light curves as likely to be observed by future time domain surveys by using an existing eclipsing binary light-curve model accounting for the change in orbital period due to gravitational radiation. We find that a search with $\dot{P}$ values is necessary for detecting binaries at orbital periods less than ∼10 min. We also show it is useful in finding and characterizing binaries with longer periods, but at a higher computational cost. Our code is called gce (GPU-accelerated Conditional Entropy). It is available on Github (https://github.com/mikekatz04/gce).


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