A tool for detection of single nucleotide polymorphism (SNP) and short insertions and deletions (indels) in data from single-cell sequencing.
Genetic variation; DNA polymorphism
Dong X, Zhang L, Milholland B, Lee M, Maslov AY, Wang T, Vijg J "Accurate identification of single-nucleotide variants in whole-genome-amplified single cells." Nat Methods. 2017 May;14(5):491-493. https://doi.org/10.1038/nmeth.4227
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