* added simple VCF merger * better clustering where large deletions are involved (with new max_alleles_per_cluster option) * bug fixes involving recognising that in indel can be represented in more than one way in a VCF file (eg homopolymers)
0.2.0
* new option `merge_method` when clustering. Let's you choose between existing gramtools method, and a simple merging of VCF records, without enumerating through all combinations
* bug fix where some combinations of variants were missed when clustering
0.1.1
Fix typo in vcf_file_read.vcf_file_to_dict(). Option renamed remove_useless_start_nulceotides -> remove_useless_start_nucleotides
0.1.0
New method: VcfRecord. called_alts_from_genotype()