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miRanda. Use miRanda software to detect potential miRNA target sites in your genomic sequences. Sequences. Mature miRNA Sequences. FASTA format. Target Sequences. FASTA format. Limit: 1,000. Use sample data.
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History - miRanda - RegenDbase
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Statistics (Release 2017-12-07) RegenDbase contains gene and...
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Sep 2, 2016 · Detailed information about target genes, target processes, and open-source software for target prediction (miRanda) is available at http://www.microrna.org. Our analysis suggests that miRNA genes, which are about 1% of all human genes, regulate protein production for 10% or more of all human genes.
Some of these projects involve: characterizing the genomes of endangered abalone species, assessing the cellular roles of small RNAs in nematodes, creating user-friendly bioinformatics tutorials, assessing transposition in irradiated maize, trans-splicing in nematodes, etc.
Feb 18, 2024 · miRanda is an algorithm for finding genomic targets for microRNAs. This algorithm has been written in C and is available as an open-source method under the GPL. miRanda reads RNA sequences (such as microRNAs) from file1 and genomic DNA/RNA sequences from file2. Both of these files should be in FASTA format.
Dec 9, 2016 · We also describe the prediction methods used by the most frequently used tools TargetScan, miRanda and DIANA microT, explaining each parameter in the search results. Finally, we offer some considerations for using a miRNA analysis tool.
- Ángela L Riffo-Campos, Ismael Riquelme, Priscilla Brebi-Mieville
- 10.3390/ijms17121987
- 2016
- Int J Mol Sci. 2016 Dec; 17(12): 1987.
To access the miRanda 3.3a tool(s) on the cluster, you first need to type the following command: module load miRanda/3.3a You can find more information on the usage of the module system at the Institut Pasteur here
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What is Miranda and how does it work?
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What is sequence-based miRNA target prediction?
miRanda is an algorithm for the detection of potential microRNA target sites in genomic sequences. miRanda reads RNA sequences (such as microRNAs) from file1 and genomic DNA/RNA sequences from file2. Both of these files should be in FASTA format.