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<p>events, as well as balanced inversions, and copy-number balanced or imbalanced translocations." Structural variant calls made by Strand-seq are resolved by chromosome-length <a href="page.php?w=haplotype">haplotype</a>, which provides additional variant calling specificity. As a current limitation, Strand-seq requires dividing cells for strand-specific labelling using <a href="page.php?w=bromodeoxyuridine">bromodeoxyuridine</a> (BrdU), and the method does not detect variants smaller than 200kb in size, such as <a href="page.php?w=Mobile_genetic_elements">mobile element insertions</a>.</p><p>
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