Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Author:
Funder
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://www.nature.com/articles/s41588-022-01087-y.pdf
Reference82 articles.
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3. Claussnitzer, M. et al. A brief history of human disease genetics. Nature 577, 179–189 (2020).
4. Benner, C. et al. FINEMAP: efficient variable selection using summary data from genome-wide association studies. Bioinformatics 32, 1493–1501 (2016).
5. Schaid, D. J., Chen, W. & Larson, N. B. From genome-wide associations to candidate causal variants by statistical fine-mapping. Nat. Rev. Genet. 19, 491–504 (2018).
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