A carregar...

Quadruplex MAPH: improvement of throughput in high-resolution copy number screening

BACKGROUND: Copy number variation (CNV) in the human genome is recognised as a widespread and important source of human genetic variation. Now the challenge is to screen for these CNVs at high resolution in a reliable, accurate and cost-effective way. RESULTS: Multiplex Amplifiable Probe Hybridisati...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Tyson, Jess, Majerus, Tamsin MO, Walker, Susan, Armour, John AL
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2761424/
https://ncbi.nlm.nih.gov/pubmed/19785739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-10-453
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!