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Error correction in single-cell DNA sequencing: finding rare allele for MRD clone


Kim Dong, MS

To improve variant calling and minimal residual disease (MRD) detection we developed a novel consensus sequence-based method for correcting the errors and reducing the false-positive rates.


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High Throughput Single Cell Analysis Workflow for Accurate Measurement of Genotoxicity Arising from Gene Editing Experiments
Saurabh Gulati
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Navigating Heterogeneity in Genome Editing Outcomes Using Single-cell Analysis
Brittany Enzmann
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Single-Cell Multi-Omic Correlation of Single Nucleotide Variants, Copy Number Variation, and Surface Epitopes for Clonal Profiling of Myeloma
Adam Sciambi; Indira Krishnan; Ben Geller; Daniel Mendoza; Chenchen Yang; Charlie Murphy; Cedric Dos Santos; Vivek S. Chopra; Habib Hamidi; Michael Nixon; Yann Nouet; Todd Druley; Herve Avet-Loiseau
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Decoding the mosaicism of genome editing with single-cell multi-omics analysis
Saurabh Gulaiti
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Why Single Cell SNV SNV + CNV DNA + Protein
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