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allow you to assemble and align your NGS data with unsurpassed ease and speed, so that you can focus on the results. No more switching between software tools to assemble sequences, identify important variants, and determine differentially expressed genes. Everything you need is here.
SeqNinja makes it easy to edit large groups of sequences and annotations simultaneously using customizable templates for functions such as translation and format conversion.
SeqNinja
Like you, we don’t have time to sit in front of our computers all day editing or annotating huge lists of sequences. That’s why we developed SeqNinja, an effortless way to batch edit genome sequences and annotations. SeqNinja can finish a day’s worth of sequence editing in a few minutes!
and provides extensive post-assembly analysis tools for both Sanger and NGS assemblies. When compared to the competition, our algorithm does the best job assembling Sanger sequences into a single contig, and calling the most accurate consensus sequence based on trace quality and shape.
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