I am using a workflow of manta + svimmer + graphtyper to identify structural variants (SVs) from short read whole genome resequencing data.
I have applied this pipeline to four types of datasets: (1) comparisons between different species (wild rodents), (2) domesticated cattle versus wild cattle, (3) comparisons between different species (wild birds), and (4) comparisons among different populations within the same species (wild birds, with an estimated divergence time of around 10,000 years).
The pipeline performs well on the first three types of datasets. However, for different populations within the same species (wild birds), it produces a large number of false positives, which is inconsistent with manual inspection in IGV.