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RMBase v2.0 has been developed, RMBase v2.0 is freely available at http://rna.sysu.edu.cn/rmbase/
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RNA modifications in sex determination and nervous system
two papers published in nature journal discovered RNA modifications modulate neuronal functions and sex determination in Drosophila.
(1) Lence T et al. m(6)A modulates neuronal functions and sex determination in Drosophila. Nature. 2016 Dec 8;540(7632):242-247.
(2) Haussmann et al. m(6)A potentiates Sxl alternative pre-mRNA splicing for robust Drosophila sex determination. Nature. 2016 Dec 8;540(7632):301-304.
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RNA modification Database and RNA-Binding Protein Binding Sites
Recently, we integrated thousands of RNA-Binding Proteins (RBP) binding sites identified from CLIP-Seq experiments and performed relationship analysis of RBP binding regions and RNA modifications. RMBase demonstrated thousands of RNA modifications located within RNA-Binding Proteins (RBPs) regions and revealed that RNA modifications may influence the function of RBP or the RBP may catalyse the RNA modification.
You can browse various RNA modifications within the RNA-Binding Proteins (RBPs) Binding sites with follow website: http://rna.sysu.edu.cn/rmbase/modRBP.phpLast edited by rnaNGS; 09-01-2017, 02:16 AM.
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recently, one Nature paper and one Nature Chemical biology paper have identified dynamic N1-methyladenosine (m1A) methylome in the message RNAs (mRNAs) using newly developed sequencing approaches. these modifications indicate a functional role for m1A in promoting translation of methylated mRNA.
(1) The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA. Nature. 2016 Feb 25;530(7591):441-6.
(2) Transcriptome-wide mapping reveals reversible and dynamic N1-methyladenosine methylome.Nat Chem Biol. 2016 Feb 10.
This datasets will be added into RMBase.
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The landscape of RNA modifications from high-throughput sequencing data
We're pleased to announce the release of the RMBase (RNA Modification Base) for decoding the landscape of RNA modifications identified from 404 high-throughput sequencing data (Pseudo-seq, Ψ-seq, CeU-seq, Aza-IP, MeRIP-seq, m6A-seq, miCLIP, m6A-CLIP, RiboMeth-seq).
It contains ~124200 N6-Methyladenosines (m6A), ~9500 pseudouridine (Ψ) modifications, ~1000 5-methylcytosine (m5C) modifications, ~1210 2′-O-methylations (2′-O-Me) and ~3130 other types of RNA modifications.
RMBase demonstrated thousands of RNA modifications located within regulatory RNAs (e.g. mRNAs, lncRNAs, miRNAs, pseudogenes, circRNAs, snoRNAs etc.), miRNA target sites and disease-related SNPs.
We hope this platform will greatly help biologists to explore the prevalence, mechanism and function of various RNA modifications and link them with human cancers and other diseases.
RMBase is freely available at http://rna.sysu.edu.cn/rmbase/. We are looking forward to hearing your feedback!
RMBase paper is available at http://nar.oxfordjournals.org/content/44/D1/D259
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by seqadmin
Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
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