Cataloging coding sequence variations in human genome databases

Biochemistry, Genetics and Molecular Biology

• Data Base 100%
• Gene Mutation 50%
• Bioinformatics 33%
• Haplotype Map 16%
• Protein Function 16%
• Human Genome 16%
• Documentation 16%
• Phenotype 8%
• Mutation 8%
• Single-Nucleotide Polymorphism 8%
• Growth 8%
• Reference Database 8%
• Introspection 8%
• Protein 8%