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Paper Details

Identification of single nucleotide variants using position-specific error estimation in deep sequencing data.
BMC Med Genomics
8
2019
SNV, SNVs, amplicon-based libraries, cancer, circulating tumor DNA samples, genomic positions, single nucleotide variants
Author NameAffiliation
Marco PuntaThe Institute of Cancer Research
Gerhardt AttardUCL Cancer Institute, University College London
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Release 1.2