AI Article Synopsis

  • Cross-contamination of cell lines is a significant issue in research, but short tandem repeats (STR) analysis has served as a reliable method for authenticating these cell lines for over two decades.
  • A new comparison of 21-loci STR methods versus the traditional 9-loci approach shows a dramatic 97.5% reduction in uncertainty for cell line authentication, effectively minimizing false positives.
  • The study highlights that using the additional loci not only enhances the specificity of markers but also suggests that updating STR databases with more loci could improve the overall accuracy and efficiency of cell line authentication, thereby reducing experimental costs.

Article Abstract

Cross-contamination of cell lines is a highly relevant and pervasive problem. The analysis of short tandem repeats (STR) is a simple and commercially available technique to authenticate cell lines for more than two decades. At present, STR multiple amplification kits have been developed up to 21 loci while the current STR databases only provide 9-loci STR profiles. Here, we compared the advantages of 21-loci STR methodology using the same algorithm as 9-loci method. The 21-loci method reduced the uncertainty ratio for authentications by 97.5% relative to the 9-loci method and exclude effectively false positive. We show that the additional 12 loci helped to greatly reduce sample-site marker specificity arising from genetic isolation and the occurrence of null alleles, suggesting that inclusion of additional loci in these databases will ultimately improve the efficiency and accuracy of authentication of cell lines. Taken together, we demonstrate the utility of a 21-loci method in human cells, providing a novel marker panel for use as a valuable alternative to 9-loci analyses to minimize cell line authentication errors and reduce costs due to erroneous experiments.

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http://dx.doi.org/10.1016/j.gene.2020.145048DOI Listing

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