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GINDEL: accurate genotype calling of insertions and deletions from low coverage population sequence reads.

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Academic year: 2017

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Figure 1 gives examples of mapped split-reads. Split-reads mapping has been used in the programs Pindel [5], SVseq [6, 7] and PRISM [8] for finding deletions.
Figure 2. Illustration of classification-based genotype calling with the real 1000 Genomes Project data
Table 1. List of features used to call genotypes of insertions and deletions.
Table 2. Comparison of GINDEL, two versions of Genome STRiP (with different setting of the effective length threshold), Pindel and Clever-sv on simulated data.
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