GenomeVX is a bioinformatics solution towards the field of Genomics. GenomeVX helps in understanding Genome-wide comparative analyses of different human populations, as well as between species, focusing on association studies relating genetic variation to disease with evidence of mutations. GenomeVX extracts data from the fields in VCF file (generated by the Genome 1000 Browser) and displays alleles for the substitutions and variations (SNP).
DEPARTMENT OF NEUROBIOLOGY & GENETICS, Biocenter, Universit of Wuerzburg
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