New release with:
- Support for variant calling on 10x Genomics linked-reads sequencing data (via --linked-reads,-J parameter).
- Somatic variants on multiple haplotypes are flagged with the "MulitHP" in the FILTER column.
- Haplotypes read counts for the ref and alt alleles reported using HPR and HPA respectively in the FORMAT field.
- List of barcodes supporting the variants are also reported in the FORMAT field.