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Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis

Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage and length. CNVs comprise a large proportion of variation in human genomes and impact health conditions. To detect rare CNV associations, kernel-based methods have been shown to be a powerful tool...

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Dades bibliogràfiques
Publicat a:PLoS Comput Biol
Autors principals: Brucker, Amanda, Lu, Wenbin, Marceau West, Rachel, Yu, Qi-You, Hsiao, Chuhsing Kate, Hsiao, Tzu-Hung, Lin, Ching-Heng, Magnusson, Patrik K. E., Sullivan, Patrick F., Szatkiewicz, Jin P., Lu, Tzu-Pin, Tzeng, Jung-Ying
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7224564/
https://ncbi.nlm.nih.gov/pubmed/32365089
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1007797
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