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Digital multiplex ligation assay for highly multiplexed screening of β-lactamase-encoding genes in bacterial isolates
2020
Communications Biology
Increasing incidence of antibiotic resistance in clinical and environmental settings calls for increased scalability in their surveillance. Current screening technologies are limited by the number of samples and genes that can easily be screened. We demonstrate here digital multiplex ligation assay (dMLA) as a low-cost targeted genomic detection workflow capable of highly-parallel screening of bacterial isolates for multiple target gene regions simultaneously. Here, dMLA is used for
doi:10.1038/s42003-020-0980-7
pmid:32451431
fatcat:y7hi3bkxdfasfklmfxnzmireyi