Abstract

Translocations and gross gene deletions are an important cause of both cancer and inherited disease. Such DNA rearrangements are nonrandomly distributed in the human genome as a consequence of selection for growth advantage and/or the inherent potential of some DNA sequences to be particularly susceptible to breakage and recombination. The Gross Rearrangement Breakpoint Database (GRaBD; http://www.uwcm.ac.uk/uwcm/mg/grabd/) was established primarily for the analysis of the sequence context of translocation and deletion breakpoints in a search for characteristics that might have rendered these sequences prone to rearrangement. GRaBD, which contains 397 germline and somatic DNA breakpoint junction sequences derived from 219 different rearrangements underlying human inherited disease and cancer, is the only comprehensive collection of gross gene rearrangement breakpoint junctions currently available.

Keywords

BreakpointBiologyGeneticsGene rearrangementContext (archaeology)GenomeGeneChromosomal translocationDNA sequencingHuman genomeGermline

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Publication Info

Year
2004
Type
review
Volume
23
Issue
3
Pages
219-221
Citations
24
Access
Closed

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Shaun S. Abeysinghe, Peter D. Stenson, Michael Krawczak et al. (2004). Gross rearrangement breakpoint database (GRaBD?). Human Mutation , 23 (3) , 219-221. https://doi.org/10.1002/humu.20006

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DOI
10.1002/humu.20006