Product introduction
Genome resequencing refers to the sequencing of the genomes of different individuals of species with known genome sequences to obtain individual or population differences by comparison with reference genome sequences.
Nanopore sequencing can directly span structural variation sites due to the long read length, and can detect structural variation (SV) in large segments, including insertions, deletions, inversions, translocations, and other sequences in large segments.
Accurate detection of structural variants in large segments（Stancu MC et al,）
Distribution of SV on chromosomes（Alonge M et al, 2020）
Publications
Stancu MC, Roosmalen MJ, Renkens I et al. Mapping and phasing of structural variation in patient genomes using nanopore sequencing. Nature Communications, 2017.
Alonge M, Wang X, Benoit M et al. Major impacts of widespread structural variation on gene expression and crop improvement in tomato. Cell, 2020.
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