We're diploid. Conventional Illumina sequencing provides a merge of the two copies of each chromosome. Arima can provide chromosome-spanning haplotypes. No N50 statistics--the whole chromosome with >93% of the SNVs phased with >99% accuracy. And our technology captures 3D genome information that allows us to place the 90% of GWAS hits that are non-coding with actionable coding regions. We start with cells and provide Illumina-compatible sequencing libraries. Now you can map your data on a real genome--a diploid genome.
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