Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide …

Mar 13, 2023 · From the Delly2 Home Page: Delly2 is an integrated structural variant prediction method that can discover and genotype deletions, tandem duplications, inversions and …

Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide …

Sep 3, 2012 · Results: We have developed an SV discovery method, called DELLY, that integrates short insert paired-ends, long-range mate-pairs and split-read alignments to …

This document provides a comprehensive overview of Delly, an integrated structural variant (SV) and copy-number variant (CNV) discovery toolkit for analyzing genomic sequencing data.

delly is an integrated structural variant prediction method that can detect deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read …

Delly is available as a Bioconda package, as a statically linked binary from the GitHub release page or as a minimal Docker container. Please have a look at Delly’s documentation for any …

Jan 1, 2026 · Delly is an integrated structural variant (SV) predictionmethod that can discover, genotype and visualize deletions, tandem duplications,inversions and translocations at single …

Delly2's capability to detect simple and complex SVs, including copy-number variations, deletions, tandem duplications, inversions, and reciprocal translocations, makes it a versatile tool for …

Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide …