Unprecedented access to haplotype-resolved biology enabled by ultra-long reads and Pore-C
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Long nanopore reads contain phase information proportional to their length, which can be used to phase small nucleotide and structural variants as well as epigenetic modifications
Download the poster to discover:
- How the combination of long and ultra-long reads with highly accurate calling of SNPs simplifies phasing and results in exceptionally long phase-blocks
- How co-phasing of variants and imprinted regions with ultra-long and Pore-C reads allows parent-of-origin inference from a single sample – with no parental sequencing required
