𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Central mutation databases—A review

✍ Scribed by Christopher J. Porter; C. Conover Talbot; Jr.; A. Jamie Cuticchia

Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
244 KB
Volume
15
Category
Article
ISSN
1059-7794

No coin nor oath required. For personal study only.

✦ Synopsis

The Internet has been a key component in the coordination of the diverse group of scientists involved in the Human Genome Project. Nowhere has this contribution been more critical than in the maintenance and exchange of information about genetic variation and mutation. Whereas the majority of DNA sequence is generated and stored by a relatively few sites, a far greater number of researchers investigate the variations in that sequence from sites scattered worldwide. It falls to central databases to utilize the Internet to assemble data from these sites and make them available to the greater human genomic community.

📜 SIMILAR VOLUMES

A review of green product databases
A review of green product databases
✍ Nimse, Prachi ;Vijayan, Abhilash ;Kumar, Ashok ;Varadarajan, Charanya 📂 Article 📅 2007 🏛 American Institute of Chemical Engineers 🌐 English ⚖ 118 KB
Website Review: pathway databases
Website Review: pathway databases
✍ Jo Wixon 📂 Article 📅 2001 🏛 Hindawi Publishing Corporation 🌐 English ⚖ 362 KB 👁 1 views

## MetaCyc and EcoCyc http://ecocyc.org The EcoCyc database of E. coli metabolic, transport and genetic regulatory networks is structured according to an ontology and consists of a web of frames (objects, eg. genes) stored in a frame knowledge representation system (Karp, 2001). Connections betwe

Single median maxillary central incisor:
Single median maxillary central incisor: New data and mutation review
✍ Kênia B. El-Jaick; Renata F. Fonseca; Miguel A. Moreira; Márcia G. Ribeiro; Ana 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 193 KB

## Abstract **BACKGROUND:** Single median maxillary central incisor (SMMCI) is a rare anomaly that may occur alone or associated with other conditions, frequently as part of the holoprosencephaly (HPE) spectrum. However, it has been suggested that SMMCI alone, or associated with some midline defect

Patient-specific mutation databases for
Patient-specific mutation databases for oral cancer
✍ M. Partridge; G. Emilion; M. Falworth; R. A'Hern; E. Phillips; S. Pateromichelak 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 French ⚖ 239 KB 👁 2 views

Development of databases, summarising the genetic events associated with oral squamous cell carcinoma (SCC), should increase our understanding of the molecular basis of these lesions. Additionally, databases will help establish whether different cancer subtypes show different growth characteristics,

UMD (Universal Mutation Database): A gen
UMD (Universal Mutation Database): A generic software to build and analyze locus-specific databases
✍ Christophe Béroud; Gwenaëlle Collod-Béroud; Catherine Boileau; Thierry Soussi; C 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 234 KB

The human genome is thought to contain about 80,000 genes and presently only 3,000 are known to be implicated in genetic diseases. In the near future, the entire sequence of the human genome will be available and the development of new methods for point mutation detection will lead to a huge increas