| Literature DB >> 26994965 |
Jonathan Seguin1, Patricia Otten2, Loïc Baerlocher2, Laurent Farinelli2, Mikhail M Pooggin3.
Abstract
In most eukaryotes, small RNA (sRNA) molecules such as miRNAs, siRNAs and piRNAs regulate gene expression and repress transposons and viruses. AGO/PIWI family proteins sort functional sRNAs based on size, 5'-nucleotide and other sequence features. In plants and some animals, viral sRNAs are extremely diverse and cover the entire viral genome sequences, which allows for de novo reconstruction of a complete viral genome by deep sequencing and bioinformatics analysis of viral sRNAs. Previously, we have developed a tool MISIS to view and analyze sRNA maps of viruses and cellular genome regions which spawn multiple sRNAs. Here we describe a new release of MISIS, MISIS-2, which enables to determine and visualize a consensus sequence and count sRNAs of any chosen sizes and 5'-terminal nucleotide identities. Furthermore we demonstrate the utility of MISIS-2 for identification of single nucleotide polymorphisms (SNPs) at each position of a reference sequence and reconstruction of a consensus master genome in evolving viral quasispecies. MISIS-2 is a Java standalone program. It is freely available along with the source code at the website http://www.fasteris.com/apps.Entities:
Keywords: Bioinformatics tool; Consensus sequence; Single nucleotide polymorphism; Small RNA; Viral quasispecies; siRNA
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Year: 2016 PMID: 26994965 DOI: 10.1016/j.jviromet.2016.03.005
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014