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2024 | 1 |
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Bioinformatics of germline variant discovery for rare disease diagnostics: current approaches and remaining challenges.
Brief Bioinform. 2024 Jan 22;25(2):bbad508. doi: 10.1093/bib/bbad508.
Brief Bioinform. 2024.
PMID: 38271481
Free PMC article.
Review.
Identification of Genetic Risk Factors of Severe COVID-19 Using Extensive Phenotypic Data: A Proof-of-Concept Study in a Cohort of Russian Patients.
Shcherbak SG, Changalidi AI, Barbitoff YA, Anisenkova AY, Mosenko SV, Asaulenko ZP, Tsay VV, Polev DE, Kalinin RS, Eismont YA, Glotov AS, Garbuzov EY, Chernov AN, Klitsenko OA, Ushakov MO, Shikov AE, Urazov SP, Baranov VS, Glotov OS.
Shcherbak SG, et al. Among authors: ushakov mo.
Genes (Basel). 2022 Mar 17;13(3):534. doi: 10.3390/genes13030534.
Genes (Basel). 2022.
PMID: 35328087
Free PMC article.
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