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S25 Strategies in complex disease mapping
S37 Industrialscale genomicsbased drug design and discovery
S43 Clinical application of pharmacogenetics
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allele frequency allele-specific allelic variants amplicons amplification analysis of genetic approach array assay association studies automated Bioarray biological Biotechnology candidate genes cleavage CodeLink common disease complex disease compound cSNPs databases detection diabetes disease genes disorders DNA sequence drug development drug discovery drug response effect fluorescent folds function gene expression genetic analysis genetic variation Genome Res haplotype high-throughput Human Genome Project hybridization identify impact individuals interactions large numbers linkage disequilibrium loci MALDI MALDI-TOF MALDI-TOF mass spectrometry mass spectrometry matrix-assisted laser methods minisequencing molecular molecules monogenic disorders Motorola mRNA multiplex mutations Nat.Genet non-synonymous oligo oligonucleotide optimization patients PCR products peptide nucleic acid personalized medicine pharmaceutical industry pharmacogenetics phenotypes polymerase polymorphisms SNPs population potential predict primer probes Proc profiling proteomics reaction risk sample screening single nucleotide polymorphisms SNP analysis SNP discovery SNP genotyping specific strategies therapeutic therapy throughput validation