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<!-- [](https://dx.doi.org/10.1093/bioinformatics/btaa963) -->
* Fix variant calling close to start/end boundaries of chromosomes
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* Add `--out-sv-rnames` and `--out-som-sv-rnames` to output SV-supporing read names (tag: `SVREADS`) in FORMAT field of VCF
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* Add `CLEAN` INFO tag for variants in clean regions, i.e., SNPs or simple small indels (≤5bp) in non-repetitive regions which are generally more reliable, to help with downstream filtering and benchmarking
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```sh
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# Download pre-built executables and test data (recommended)
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