A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer

We aimed to examine the associations of a genome‐wide set of single nucleotide polymorphisms (SNPs) and 254 copy number variations (CNVs) and/or insertion/deletions (INDELs) with clinical outcomes in colorectal cancer patients (n = 505). We also aimed to investigate whether their associations change...

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Detalles Bibliográficos
Autores principales: Yu, Yajun, Werdyani, Salem, Carey, Megan, Parfrey, Patrick, Yilmaz, Yildiz E., Savas, Sevtap
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637572/
https://www.ncbi.nlm.nih.gov/pubmed/34309201
http://dx.doi.org/10.1002/1878-0261.13067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637572/
https://www.ncbi.nlm.nih.gov/pubmed/34309201
http://dx.doi.org/10.1002/1878-0261.13067

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