End-to-end workflow for haplotype-resolved genetic and epigenetic variant calling using nanopore sequencing

Comprehensive identification and interpretation of single nucleotide variants (SNVs), structural variants (SVs), copy number variants (CNVs), and epigenetic modifications from a single PromethIONTM Flow Cell.

Download the poster to find out:

• How nanopore sequencing accuracy and read lengths enable calling and phasing of small nucleotide variants with high sensitivity and specificity, even in difficult genomic regions

• How long, native nanopore reads enable precise calling of phased SVs, CNVs repeat expansions, and 5mC and 5hmC in a single assay