scholarly journals AQMM: Enabling Absolute Quantification of Metagenome and Metatranscriptome

2017 ◽  
Author(s):  
Xiao-Tao Jiang ◽  
Ke Yu ◽  
Li-Guan Li ◽  
Xiao-Le Yin ◽  
An-Dong Li ◽  
...  

AbstractMetatranscriptome has become increasingly important along with the application of next generation sequencing in the studies of microbial functional gene activity in environmental samples. However, the quantification of target active gene is hindered by the current relative quantification methods, especially when tracking the sharp environmental change. Great needs are here for an easy-to-perform method to obtain the absolute quantification. By borrowing information from the parallel metagenome, an absolute quantification method for both metagenomic and metatranscriptomic data to per gene/cell/volume/gram level was developed. The effectiveness of AQMM was validated by simulated experiments and was demonstrated with a real experimental design of comparing activated sludge with and without foaming. Our method provides a novel bioinformatic approach to fast and accurately conduct absolute quantification of metagenome and metatranscriptome in environmental samples. The AQMM can be accessed from https://github.com/biofuture/aqmm.

2021 ◽  
Author(s):  
Carel Jacobus van Heerden ◽  
Phylli Burger ◽  
Johan Theodorus Burger ◽  
Renée Prins

Powdery and downy mildew have a large negative impact on grape production worldwide. Quantitative trait loci (QTL) mapping projects have identified several loci for the genetic factors responsible for resistance to these pathogens. Several of these studies have focused on the cultivar Regent, which carries the resistance loci to downy mildew on chromosome 18 (Rpv3), as well powdery mildew on chromosome 15 (Ren3, Ren9). Several other minor resistance loci have also been identified on other chromosomes. Here we report on the re-sequencing of the Regent and Red Globe (susceptible) genomes using next generation sequencing. While the genome of Regent has more SNP variants than Red Globe, the distribution of these variants across the two genomes is not the same, nor is it uniform. The variation per gene shows that some genes have higher SNP density than others and that the number of SNPs for a given gene is not always the same for the two cultivars. In this study, we investigate the effectiveness of studying the variation of non-synonymous to synonymous SNP ratio's between resistant and susceptible cultivars in the target QTL regions as a strategy to narrow down the number of likely candidate genes for Rpv3, Ren3 and Ren9.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4227 ◽  
Author(s):  
Saima Sultana Tithi ◽  
Frank O. Aylward ◽  
Roderick V. Jensen ◽  
Liqing Zhang

With the increase in the availability of metagenomic data generated by next generation sequencing, there is an urgent need for fast and accurate tools for identifying viruses in host-associated and environmental samples. In this paper, we developed a stand-alone pipeline called FastViromeExplorer for the detection and abundance quantification of viruses and phages in large metagenomic datasets by performing rapid searches of virus and phage sequence databases. Both simulated and real data from human microbiome and ocean environmental samples are used to validate FastViromeExplorer as a reliable tool to quickly and accurately identify viruses and their abundances in large datasets.


Author(s):  
Peter A. C. 't Hoen ◽  
Matthew S. Hestand ◽  
Judith M. Boer ◽  
Yuching Lai ◽  
Maarten van Iterson ◽  
...  

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