ntEdit v1.4.2

VCF input to help identify variants of clinical significance
Includes option to supply a VCF input file to ntEdit, for cross-referencing base variants
For instance, users may wish to identify annotated clinical variants (e.g., ClinVar) in their genomics datasets, together with the -s 1 option
*To make the ntEdit output VCF easier to parse, v1.4.2 replaced the delimiter from pipe | to caret ^ since clinvar records have both pipes | and semicolons ; in their VCF INFO descriptions