Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing

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Figure 3.
Figure 3.

Structural variation inference on down-sampled long-read data sets. (A) Workflow for down-sampling full long-read data set and computing concordance between down-sampled and full coverage data sets with distinct minimum fractional x/y read support for an SV to be considered. (B) Precision and recall for SVs inferred on down-sampled ONT and PacBio data for sample 51T. SVs inferred on the full coverage data set at the matching read support threshold are used as the ground truth.

This Article

  1. Published in Advance September 4, 2020, doi: 10.1101/gr.260497.119 Genome Res. 30: 1258-1273

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