v0.1-r11
- Variant calling ~2.5x faster than
v0.1-r10
tested with ONT Q20 data, with feature generation in both pileup and full-alignment now implemented in C (co-contributors @cjw85, @ftostevin-ont, @EpiSlim). - Added the lightning-fast longphase as an option for phasing. Enable using
longphase
with option--longphase_for_phasing
. New option is disabled by default to align with the default behavior of the previous versions, but we recommend enable when calling human variants with ≥20x long-reads). - Added
--min_coverage
and--min_mq
options (#83). - Added
--min_contig_size
option to skip calling variants in short contigs when using genome assembly as input. - Reads haplotagging after phasing before full-alignment calling now integrated into full-alignment calling to avoid generating an intermediate BAM file.
- Supported .
csi
BAM index for large references (#90). For more speedup details, please check Notes on r11.
v0.1-r11 minor 2 patches are included in all installation options