Deyan Yosifov (@deyan-yosifov.bsky.social)

Our latest publication shares our experience of using only tNGS data from a routine diagnostic panel for SNP-based detection of sample swaps or sample mislabelling, and includes an R function for easy comparison of samples: bmcresnotes.biomedcentral.com/articles/10....

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Genotyping from targeted NGS data based on a small set of SNPs correctly matches patient samples - BMC Research Notes Objective Mislabelling and swapping of laboratory samples are handling errors that can lead to erroneous interpretation of data and/or patient harm. Sequenced samples can be traced back to the respect... https://bmcresnotes.biomedcentral.com/articles/10.1186/s13104-025-07348-3