The Human Gene Mutation Database (HGMD®) is a comprehensive core collection of germline mutations in nuclear genes that underlie or are associated with human inherited disease. Here, we summarize the history of the database and its current resources. By December 2008, the database contained over 85,000 different lesions detected in 3,253 different genes, with new entries currently accumulating at a rate exceeding 9,000 per annum. Although originally established for the scientific study of mutational mechanisms in human genes, HGMD has since acquired a much broader utility for researchers, physicians, clinicians and genetic counselors as well as for companies specializing in biopharmaceuticals, bioinformatics and personalized genomics. HGMD ...
International audienceCommunicated by Marc Greenblatt With the completion of the Human Genome Projec...
Genetics is concerned with inheritance, genomics with the study of genomes. Bioinformatics provides ...
This talk is based on our paper: Li MJ, Wang P, Liu X, Lim EL, Wang Z, Yeager M, Wong MP, Sham PC, C...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
The Human Gene Mutation Database (HGMD®) is a comprehensive collection of germline mutations in nucl...
The Human Gene Mutation Database (HGMD) represents a comprehensive core collection of data on publis...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The HumanGeneMutation Database (HGMD) represents a comprehensive core collection of data on publishe...
Although 20 years have elapsed since the first single basepair substitution underlying an inherited ...
Databases of mutations causing Mendelian disease play a crucial role in research, diagnostic and gen...
The human genome is thought to contain about 80,000 genes and presently only 3,000 are known to be i...
Abstract no. 90INTRODUCTION: During the past few years, more than 10,000 single-nucleotide polymorph...
International audienceCommunicated by Marc Greenblatt With the completion of the Human Genome Projec...
Genetics is concerned with inheritance, genomics with the study of genomes. Bioinformatics provides ...
This talk is based on our paper: Li MJ, Wang P, Liu X, Lim EL, Wang Z, Yeager M, Wong MP, Sham PC, C...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
The Human Gene Mutation Database (HGMD®) is a comprehensive collection of germline mutations in nucl...
The Human Gene Mutation Database (HGMD) represents a comprehensive core collection of data on publis...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
The HumanGeneMutation Database (HGMD) represents a comprehensive core collection of data on publishe...
Although 20 years have elapsed since the first single basepair substitution underlying an inherited ...
Databases of mutations causing Mendelian disease play a crucial role in research, diagnostic and gen...
The human genome is thought to contain about 80,000 genes and presently only 3,000 are known to be i...
Abstract no. 90INTRODUCTION: During the past few years, more than 10,000 single-nucleotide polymorph...
International audienceCommunicated by Marc Greenblatt With the completion of the Human Genome Projec...
Genetics is concerned with inheritance, genomics with the study of genomes. Bioinformatics provides ...
This talk is based on our paper: Li MJ, Wang P, Liu X, Lim EL, Wang Z, Yeager M, Wong MP, Sham PC, C...