Whole genome sequence of Bacillus thuringiensis ATCC 10792 and improved discrimination of Bacillus thuringiensis from Bacillus cereus group based on novel biomarkers

2019 ◽  
Vol 129 ◽  
pp. 284-297
Author(s):  
Ramachandran Chelliah ◽  
Shuai Wei ◽  
Byung-Jae Park ◽  
Momna Rubab ◽  
Eric Banan-Mwine Dalirii ◽  
...  
2020 ◽  
Vol 202 (7) ◽  
pp. 1693-1700
Author(s):  
Weibo Ma ◽  
Huicheng Chen ◽  
Xiaoyan Jiang ◽  
Junxiang Wang ◽  
Ivan Gelbič ◽  
...  

2017 ◽  
Vol 5 (35) ◽  
Author(s):  
Chun-Hao Jiang ◽  
Yun Chen ◽  
Fang Yan ◽  
Zhi-Hang Fan ◽  
Jian-Hua Guo

ABSTRACT Bacillus cereus AR156 was originally isolated from the forest soil of Zhenjiang, a city in China. To shed new light on the molecular mechanisms underlying the biological control of soilborne pathogens, the whole genome of this strain was sequenced. Here, we report the draft genome sequence of this strain, consisting of a single circularized contig measuring 5.66 Mb, with an average GC content of 35.5% and 5,367 open reading frames.


2010 ◽  
Vol 36 (4) ◽  
pp. 688-694
Author(s):  
Yi-Jun WANG ◽  
Yan-Ping LÜ ◽  
Qin XIE ◽  
De-Xiang DENG ◽  
Yun-Long BIAN

2014 ◽  
Vol 40 (12) ◽  
pp. 2059
Author(s):  
Lin-Yi QIAO ◽  
Xin LI ◽  
Zhi-Jian CHANG ◽  
Xiao-Jun ZHANG ◽  
Hai-Xian ZHAN ◽  
...  

IDCases ◽  
2020 ◽  
pp. e01034
Author(s):  
Charlie Tan ◽  
Fang-I Lu ◽  
Patryk Aftanas ◽  
Kara Tsang ◽  
Samira Mubareka ◽  
...  

Author(s):  
Amnon Koren ◽  
Dashiell J Massey ◽  
Alexa N Bracci

Abstract Motivation Genomic DNA replicates according to a reproducible spatiotemporal program, with some loci replicating early in S phase while others replicate late. Despite being a central cellular process, DNA replication timing studies have been limited in scale due to technical challenges. Results We present TIGER (Timing Inferred from Genome Replication), a computational approach for extracting DNA replication timing information from whole genome sequence data obtained from proliferating cell samples. The presence of replicating cells in a biological specimen leads to non-uniform representation of genomic DNA that depends on the timing of replication of different genomic loci. Replication dynamics can hence be observed in genome sequence data by analyzing DNA copy number along chromosomes while accounting for other sources of sequence coverage variation. TIGER is applicable to any species with a contiguous genome assembly and rivals the quality of experimental measurements of DNA replication timing. It provides a straightforward approach for measuring replication timing and can readily be applied at scale. Availability and Implementation TIGER is available at https://github.com/TheKorenLab/TIGER. Supplementary information Supplementary data are available at Bioinformatics online


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