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Evaluation of copy number variation detection for a SNP array platform

BACKGROUND: Copy Number Variations (CNVs) are usually inferred from Single Nucleotide Polymorphism (SNP) arrays by use of some software packages based on given algorithms. However, there is no clear understanding of the performance of these software packages; it is therefore difficult to select one...

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Bibliografiska uppgifter
Huvudupphovsmän: Zhang, Xin, Du, Renqian, Li, Shilin, Zhang, Feng, Jin, Li, Wang, Hongyan
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2014
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4015297/
https://ncbi.nlm.nih.gov/pubmed/24555668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-15-50
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