BaseSpace Sequence Hub offers a wide variety 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 all of the common 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 get started using Basespace, find compatible libraries, and troubleshoot online.
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