Found: 15
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IBD Sharing between Africans, Neandertals, and Denisovans.
- Published in:
- Genome Biology & Evolution, 2016, v. 8, n. 12, p. 3406, doi. 10.1093/gbe/evw234
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- Publication type:
- Article
ATAV: a comprehensive platform for population-scale genomic analyses.
- Published in:
- BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04071-1
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- Publication type:
- Article
Family reunion via error correction: an efficient analysis of duplex sequencing data.
- Published in:
- BMC Bioinformatics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12859-020-3419-8
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- Publication type:
- Article
Genome-wide Enrichment of TERT Rare Variants in Idiopathic Pulmonary Fibrosis Patients of Latino Ancestry.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 206, n. 7, p. 903, doi. 10.1164/rccm.202203-0622LE
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- Publication type:
- Article
Rare and Common Variants in Contribute to Genetic Risk of Idiopathic Pulmonary Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 206, n. 1, p. 56, doi. 10.1164/rccm.202110-2439OC
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- Publication type:
- Article
Further delineation of putative ACTB loss‐of‐function variants: A 4‐patient series.
- Published in:
- Human Mutation, 2020, v. 41, n. 4, p. 753, doi. 10.1002/humu.23970
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- Publication type:
- Article
CSGALNACT1‐congenital disorder of glycosylation: A mild skeletal dysplasia with advanced bone age.
- Published in:
- Human Mutation, 2020, v. 41, n. 3, p. 655, doi. 10.1002/humu.23952
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- Publication type:
- Article
Rectified factor networks for biclustering of omics data.
- Published in:
- Bioinformatics, 2017, v. 33, n. 14, p. i59, doi. 10.1093/bioinformatics/btx226
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- Publication type:
- Article
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 11, p. 1, doi. 10.1371/journal.pgen.1010367
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- Publication type:
- Article
Association of rare predicted loss-of-function variants of influenza-related type I IFN genes with critical COVID-19 pneumonia. Reply.
- Published in:
- 2021
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- Publication type:
- letter
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Prevalence and significance of clonal hematopoiesis of indeterminate potential in lung transplant recipients.
- Published in:
- BMC Pulmonary Medicine, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12890-023-02703-1
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- Publication type:
- Article
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS.
- Published in:
- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-10538-1
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- Publication type:
- Article
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
- Published in:
- Nature Communications, 2023, n. 1, p. 1, doi. 10.1038/s41467-023-39539-6
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- Publication type:
- Article
panelcn.MOPS: Copy-number detection in targeted NGS panel data for clinical diagnostics.
- Published in:
- Human Mutation, 2017, v. 38, n. 7, p. 889, doi. 10.1002/humu.23237
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- Publication type:
- Article