CHRIS AMOS to DNA Copy Number Variations
This is a "connection" page, showing publications CHRIS AMOS has written about DNA Copy Number Variations.
Connection Strength
1.007
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Genome-wide algorithm for detecting CNV associations with diseases. BMC Bioinformatics. 2011 Aug 09; 12:331.
Score: 0.242
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A statistical learning method for simultaneous copy number estimation and subclone clustering with single-cell sequencing data. Genome Res. 2024 02 07; 34(1):85-93.
Score: 0.144
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BMI-CNV: a Bayesian framework for multiple genotyping platforms detection of copy number variants. Genetics. 2022 11 30; 222(4).
Score: 0.132
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Pan-cancer evaluation of gene expression and somatic alteration data for cancer prognosis prediction. BMC Cancer. 2021 Sep 25; 21(1):1053.
Score: 0.122
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Cancer prognosis prediction using somatic point mutation and copy number variation data: a comparison of gene-level and pathway-based models. BMC Bioinformatics. 2020 Oct 20; 21(1):467.
Score: 0.114
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An accurate and powerful method for copy number variation detection. Bioinformatics. 2019 09 01; 35(17):2891-2898.
Score: 0.106
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Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis. Hum Mol Genet. 2013 Mar 15; 22(6):1249-61.
Score: 0.066
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Twins, tissue, and time: an assessment of SNPs and CNVs. Twin Res Hum Genet. 2012 Dec; 15(6):737-45.
Score: 0.065
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Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet. 2012 May 06; 44(6):642-50.
Score: 0.016