Several reduced-representation bisulfite sequencing methods have been developed in recent years to determine cytosine methylation de novo in nonmodel species. Here, we present epiGBS2, a laboratory protocol based on epiGBS with a revised and userfriendly bioinformatics pipeline for a wide range of species with or without a reference genome. epiGBS2 is cost-and time-efficient and the computational workflow is designed in a user-friendly and reproducible manner. The library protocol allows a flexible choice of restriction enzymes and a double digest. The bioinformatics pipeline was integrated in the Snakemake workflow management system, which makes the pipeline easy to execute and modular, and parameter settings for important computational steps flexible. We implemented biSmark for alignment and methylation analysis and we preprocessed alignment files by double masking to enable single nucleotide polymorphism calling with FreebayeS (epiFreebayeS). The performance of several critical steps in epiGBS2 was evaluated against baseline data sets from Arabidopsis thaliana and great tit (Parus major), which confirmed its overall good performance. We provide a detailed description of the laboratory protocol and an extensive manual of the
Microsatellites are ubiquitously distributed, polymorphic repeat sequence valuable for association, selection, population structure and identification. They can be mined by genomic library, probe hybridization and sequencing of selected clones. Such approach has many limitations like biased hybridization and selection of larger repeats. In silico mining of polymorphic markers using data of various genotypes can be rapid and economical. Available tools lack in some or other aspects like: targeted user defined primer generation, polymorphism discovery using multiple sequence, size and number limits of input sequence, no option for primer generation and e-PCR evaluation, transferability, lack of complete automation and user-friendliness. They also lack the provision to evaluate published primers in e-PCR mode to generate additional allelic data using re-sequenced data of various genotypes for judicious utilization of previously generated data. We developed the tool (PolyMorphPredict) using Perl, R, Java and launched at Apache which is available at http://webtom.cabgrid.res.in/polypred/. It mines microsatellite loci and computes primers from genome/transcriptome data of any species. It can perform e-PCR using published primers for polymorphism discovery and across species transferability of microsatellite loci. Present tool has been evaluated using five species of different genome size having 21 genotypes. Though server is equipped with genomic data of three species for test run with gel simulation, but can be used for any species. Further, polymorphism predictability has been validated using in silico and in vitro PCR of four rice genotypes. This tool can accelerate the in silico microsatellite polymorphism discovery in re-sequencing projects of any species of plant and animal for their diversity estimation along with variety/breed identification, population structure, MAS, QTL and gene discovery, traceability, parentage testing, fungal diagnostics and genome finishing.
Karnal bunt disease caused by the fungus Tilletia indica Mitra is a serious concern due to strict quarantines affecting international trade of wheat. We announce here the first draft assembly of two monosporidial lines, PSWKBGH-1 and -2, of this fungus, having approximate sizes of 37.46 and 37.21 Mbp, respectively.
Objective: Development of green nanotechnology is generating interest of researchers toward eco-friendly biosynthesis of nanoparticles (NPs). In this study, biosynthesis of stable copper (Cu) NPs was done using Passiflora foetida leaf extract.
Materials and Methods:First, we prepared leaf extract of Passiflora foetida in deionized water. This extract added to 20 mMol of Cupric sulfate solution, and we observed the change in color of the solution from colorless to colored solution; this indicates that there is a formation of CuNPs.Results: These biosynthesized CuNPs were characterized with the help of ultraviolet visible spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The spectroscopic analysis of synthesized CuNPs showed the maximum absorbance at 350 nm indicating the presence of biosynthesized CuNPs in the reaction mixture.
Conclusion:It was observed that the P. foetida leaf extract can reduce Cu ions into CuNPs within 8-10 minutes of reaction time. Thus, this method can be used for rapid and eco-friendly biosynthesis of stable CuNPs.
epiGBS is an existing reduced representation bisulfite sequencing method to determine cytosine methylation and genetic polymorphisms de novo . Here, we present epiGBS2, an improved epiGBS laboratory protocol and user-friendly bioinformatics pipeline for a wide range of species with or without reference genome. epiGBS2 decreases costs and time investment and increases user-friendliness and reproducibility. The library protocol was adjusted to allow for a flexible choice of restriction enzymes and a double digest. Instead of fully methylated adapters, semi-methylated adapters are now used. The bioinformatics pipeline was improved in speed and integrated in the snakemake workflow management system, which now makes the pipeline easy to execute, modular, and parameter settings flexible. We also provide a detailed description of the laboratory protocol, an extensive manual of the bioinformatics pipeline, which is publicly accessible on github ( https://github.com/nioo-knaw/epiGBS2) and zenodo ( https://doi.org/10.5281/zenodo.3819996 ), and example output.
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