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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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| Main Authors: | , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BioMed Central
2014
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| Ábhair: | |
| Rochtain Ar Líne: | 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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