198c9b8daecc44fbda6a6494c566c723920f030a lrnassar Wed Mar 11 18:25:21 2026 -0700 Fixing a few hundred clear typos with the help of Claude. Some are less important in code comments, but majority of them are in user-facing places. I manually approved 60%+ of the changes and didn't see any that were an incorrect suggestion, at worst it was potentially uncessesary, like a code comment having cant instead of can't. No RM. diff --git src/lib/vcf.c src/lib/vcf.c index db148b4225f..3db0767f942 100644 --- src/lib/vcf.c +++ src/lib/vcf.c @@ -1597,31 +1597,31 @@ "\"The fields of a Variant Call Format data line\"" " (" " string chrom; \"An identifier from the reference genome\"" " uint pos; \"The reference position, with the 1st base having position 1\"" " string id; \"Semi-colon separated list of unique identifiers where available\"" " string ref; \"Reference base(s)\"" " string alt; \"Comma separated list of alternate non-reference alleles " "called on at least one of the samples\"" " string qual; \"Phred-scaled quality score for the assertion made in ALT. i.e. " "give -10log_10 prob(call in ALT is wrong)\"" " string filter; \"PASS if this position has passed all filters. Otherwise, a " "semicolon-separated list of codes for filters that fail\"" " string info; \"Additional information encoded as a semicolon-separated series " "of short keys with optional comma-separated values\"" " string format; \"If genotype columns are specified in header, a " - "semicolon-separated list of of short keys starting with GT\"" + "semicolon-separated list of short keys starting with GT\"" " string genotypes; \"If genotype columns are specified in header, a tab-separated " "set of genotype column values; each value is a colon-separated " "list of values corresponding to keys in the format column\"" " )"; struct asObject *vcfAsObj() // Return asObject describing fields of VCF { return asParseText(vcfDataLineAutoSqlString); } char *vcfGetSlashSepAllelesFromWords(char **words, struct dyString *dy) /* Overwrite dy with a /-separated allele string from VCF words, * skipping the extra initial base that VCF requires for indel alleles if necessary, * and trimming identical bases at the ends of all alleles if there are any.