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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224564/
https://www.ncbi.nlm.nih.gov/pubmed/32365089
http://dx.doi.org/10.1371/journal.pcbi.1007797

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224564/
https://www.ncbi.nlm.nih.gov/pubmed/32365089
http://dx.doi.org/10.1371/journal.pcbi.1007797

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