𝔖 Bobbio Scriptorium
✦   LIBER   ✦

SSRD: simple sequence repeats database of the human genome

✍ Scribed by Subbaya Subramanian; Vamsi M Madgula; Ranjan George; Satish Kumar; Madhusudhan W Pandit; Lalji Singh


Publisher
Hindawi Publishing Corporation
Year
2003
Tongue
English
Weight
70 KB
Volume
4
Category
Article
ISSN
1531-6912

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Future vision of the GDB Human Genome Da
✍ A. Jamie Cuticchia πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 180 KB πŸ‘ 2 views

In 1973, scientists assembled at the first Human Gene Mapping Workshop to discuss the 64 human genes mapped at that time. In 1989, the GDB Human Genome Database was created to store information on 1,700 mapped human genes. Ten years later, as the human genome project closes in on the release of the

The interactive online SKY/M-FISH & CGH
✍ Turid Knutsen; Vasuki Gobu; Rodger Knaus; Hesed Padilla-Nash; Meena Augustus; Ro πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 944 KB

## Abstract To catalog data on chromosomal aberrations in cancer derived from emerging molecular cytogenetic techniques and to integrate these data with genome maps, we have established two resources, the NCI and NCBI SKY/M‐FISH & CGH Database and the Cancer Chromosomes database. The goal of the fo

Repeated sequence homogenization between
✍ Luis CadahΓ­a; Wilhelm Pinsker; Juan JosΓ© Negro; Mihaela Pavlicev; Vicente Urios; πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 228 KB

## Abstract In birds, the noncoding control region (CR) and its flanking genes are the only parts of the mitochondrial (mt) genome that have been modified by intragenomic rearrangements. In raptors, two noncoding regions are present: the CR has shifted to a new position with respect to the β€œancestr

Detection of Triplet Repeat Expansion in
✍ Ko-ichi Sawada; Manabu Doyu; Fumiaki Tanaka; Gen Sobue; Kikuya Kato πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 English βš– 274 KB

Triplet repeat disease is a group of hereditary neurodegenerative disorders caused by expansion of trinucleotide repeats such as CAG/CTG, CGG/CCG, and GAA/TTC. Direct detection of the expansion in the patient's genome shortcuts the tedious process needed for identification of disease genes by conven