BaseSpace Sequence Hub offers an extensive range of next-generation sequencing (NGS) data analysis apps that are developed or optimized by Illumina, or from a growing ecosystem of third-party app providers. Together, these cover the majority of analysis methods used with Illumina NGS data, from RNA-Seq to exome/enrichment, amplicon, whole-genome sequencing (WGS), de novo assembly, 16S metagenomics, and more.
Access this informative resource to learn how to start using BaseSpace, find step-by-step instructions, see compatible libraries, and get troubleshooting tips.
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