Next-generation sequencing (NGS) has revolutionized the study of DNA variants. Watch this animation to learn how the easy and accessible Illumina NGS technology can complement your Sanger sequencing work. By using the same lab tools you are familiar with to prepare the samples for NGS, and plug-and-play bioinformatics solutions to analyse the data, you can screen more samples cost-effectively and detect multiple variants across targeted areas of the genome.
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