Found: 7
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EM-mosaic detects mosaic point mutations that contribute to congenital heart disease.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-00738-1
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- Article
Contrasting Determinants of Mutation Rates in Germline and Soma.
- Published in:
- Genetics, 2017, v. 207, n. 1, p. 255, doi. 10.1534/genetics.117.1114
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- Article
MVP predicts the pathogenicity of missense variants by deep learning.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20847-0
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- Article
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007822
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- Article
Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.
- Published in:
- Human Genetics, 2017, v. 136, n. 6, p. 679, doi. 10.1007/s00439-017-1774-y
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- Article
CFHMM: Heterogeneous Tumor CNV Classification by Hidden Markov.
- Published in:
- Columbia Undergraduate Science Journal, 2016, v. 10, p. 28
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- Publication type:
- Article
Deep Genetic Connection Between Cancer and Developmental Disorders.
- Published in:
- Human Mutation, 2016, v. 37, n. 10, p. 1042, doi. 10.1002/humu.23040
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- Article