This web tool allows you to assemble a set of contiguous sequences (contigs)
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The Wise2 form compares a protein sequence to a genomic DNA sequence, allowing for introns and frameshifting errors.
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Galaxy is an open source, web-based platform for data intensive biomedical research whose purpose is to make complex analysis more accessible. It is a useful tool for bioinformaticians and DNA sequencers. Galaxy provides a point-and-click web interface alternative to the bioinformatics command line, thus allowing researchers to easily create, run, and troubleshoot analytical pipelines (see Perkel JM, The Scientist 08/2016, p 57).
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Empowering the Development of Genomics Expertise
Category: DNA sequencing, Sequencing and assembly software
EDGE bioinformatics is intended to help truly democratize the use of Next Generation Sequencing for exploring genomes and metagenomes. Given that bioinformatic analysis is now the rate limiting factor in genomics, we developed EDGE bioinformatics with a user-friendly interface that allows scientists to perform a number of tailored analyses using many cutting-edge tools. Users can explore those and other data sets using a free demo hosted on the LANL server. Researchers who wish to analyse their
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BrowserGenome is a web-based deep-sequencing data-analysis platform offering barcode deconvolution, read mapping, real-time data visualization, transcript-count analysis and data normalization. BrowserGenome is specifically focused on the evaluation of mRNA-seq data, but it can easily be extended to other applications (Schmid-Burgk JL, Hornung V, Nature Meth 12:1001, 2015).
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VecScreen quickly identifies contaminating vectors in your sequence. VecScreen is a system that quickly finds segments of a nucleic acid sequence that may be of vector origin. It helps researchers identify and remove any segments of vector origin before they analyze or submit sequences.
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