The DNA sequence of human chromosome 22
Knowledge of the complete genomic DNA sequence of an organism allows a systematic approach to defining its genetic components. The genomic sequence provides access to the comple...
Publications
4 shownA map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
We describe a map of 1.42 million single nucleotide polymorphisms (SNPs) distributed throughout the human genome, providing an average density on available sequence of one SNP e...
COSMIC: the Catalogue Of Somatic Mutations In Cancer
This FAIRsharing record describes: The Catalogue of Somatic Mutations in Cancer (COSMIC) is a database of manually-curated somatic mutation information relating to human cancers...
The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers
The Catalogue of Somatic Mutations in Cancer (COSMIC) Cancer Gene Census (CGC) is an expert-curated description of the genes driving human cancer that is used as a standard in c...
Frequent Co-Authors
Researcher Info
- h-index
- 4
- Publications
- 4
- Citations
- 10,633
- Institution
- Wellcome Sanger Institute
External Links
Impact Metrics
h-index
4
h-index: Number of publications with at least h citations each.