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Copy Number Variation Pattern for Discriminating MACROD2 States of Colorectal Cancer Subtypes
Copy number variation (CNV) is a common structural variation pattern of DNA, and it features a higher mutation rate than single-nucleotide polymorphisms (SNPs) and affects a larger fragment of genomes. CNV is related with the genesis of complex diseases and can thus be used as a strategy to identify...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930883/ https://www.ncbi.nlm.nih.gov/pubmed/31921812 http://dx.doi.org/10.3389/fbioe.2019.00407 |