MLGA—a rapid and cost-efficient assay for gene copy-number analysis

Structural variation is an important cause of genetic variation. Whole genome analysis techniques can efficiently identify copy-number variable regions but there is a need for targeted methods, to verify and accurately size variable regions, and to diagnose large sample cohorts. We have developed a...

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Detalles Bibliográficos
Autores principales: Isaksson, Magnus, Stenberg, Johan, Dahl, Fredrik, Thuresson, Ann-Charlotte, Bondeson, Marie-Louise, Nilsson, Mats
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034490/
https://www.ncbi.nlm.nih.gov/pubmed/17823203
http://dx.doi.org/10.1093/nar/gkm651

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034490/
https://www.ncbi.nlm.nih.gov/pubmed/17823203
http://dx.doi.org/10.1093/nar/gkm651

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