1A framework for variation discovery and genotyping using next-generation DNA sequencing data2011 · 12,507 citations
2Low-coverage sequencing: Implications for design of complex trait association studies2020 · 20 citations
3Biological Sequence Analysis1998 · 3,293 citations
4MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes2020 · 79 citations
5Human Triallelic Sites: Evidence for a New Mutational Mechanism?2009 · 96 citations

Ein statistischer Rahmen für SNP-Calls, Mutationsentdeckung, Assoziationsmapping und Schätzung populationsgenetischer Parameter aus Sequenzierungsdaten | Synapse

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1A framework for variation discovery and genotyping using next-generation DNA sequencing data2011 · 12,507 citations
2Low-coverage sequencing: Implications for design of complex trait association studies2020 · 20 citations
3Biological Sequence Analysis1998 · 3,293 citations
4MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes2020 · 79 citations
5Human Triallelic Sites: Evidence for a New Mutational Mechanism?2009 · 96 citations