Changes

'''AnnoVcf''' is a [[SNP annotation]] tool for the next generation sequence data in the 1000 genome project. It takes a [[VCF]] SNP file as input and generates SNP annotation information into a VCF output

'''vcfCodingSnps''' is a [[SNP annotation]] tool that annotates coding variants in a [[VCF]] format input file. It takes a VCF as input and generates an annotated VCF file as output.