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  1. ...are shown for SCsnvcna, SCARLET, COMPASS, SiFit, SCG, RobustClone, and SiCloneFit on varying FP rate (A), varying FN rate (B), and varying missing rate (C).View larger version: In this window In a new window Figure 3. Group 2: evaluation of scalability. Genotype error, pairwise SNV error, and pairwise SNV...
  2. ....823941 ↵Zaccaria S, Raphael BJ. 2021. Characterizing allele- and haplotype-specific copy numbers in single cells with CHISEL. Nat Biotechnol 39: 207–214. doi:10.1038/s41587-020-0661-6 ↵Zafar H, Navin N, Chen K, Nakhleh L. 2019. SiCloneFit: Bayesian inference of population structure, genotype, and phylogeny...
  3. .... There already exist computational tools for identifying and decoupling doublets, in particular Single Cell Genotyper (Roth et al. 2016), which we employ in this study as a preprocessing step for the purpose of reducing their impact in our analysis. Furthermore, a recently developed tool, SiCloneFit (Zafar et al...
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