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Maximizing efficiency in sedimentary ancient DNA analysis: a novel extract pooling approach. | LitMetric

AI Article Synopsis

  • Ancient DNA research has shifted towards analyzing sedimentary ancient DNA (sedaDNA) to understand past human and mammalian populations, but the process is often slow and expensive.
  • A new high-throughput method is introduced that uses pooled testing, allowing multiple sediment samples to be analyzed simultaneously and improving efficiency in detecting ancient DNA.
  • This method has been tested successfully on sediment from various Paleolithic sites, showing the ability to find detectable aDNA signals even when mixed with negative samples, leading to up to 70% cost savings and reduced laboratory processing time.

Article Abstract

In the last few decades, the field of ancient DNA has taken a new direction towards using sedimentary ancient DNA (sedaDNA) for studying human and mammalian population dynamics as well as past ecosystems. However, the screening of numerous sediment samples from archaeological sites remains a time-consuming and costly endeavor, particularly when targeting hominin DNA. Here, we present a novel high-throughput method that facilitates the fast and efficient analysis of sediment samples by applying a pooled testing approach. This method combines multiple extracts, enabling early parallelization of laboratory procedures and effective aDNA screening. Pooled samples with detectable aDNA signals undergo detailed analysis, while empty pools are discarded. We have successfully applied our method to multiple sediment samples from Middle and Upper Paleolithic sites in Europe, Asia, and Africa. Notably, our results reveal that an aDNA signal remains discernible even when pooled with four negative samples. We also demonstrate that the DNA yield of double-stranded libraries increases significantly when reducing the extract input, potentially mitigating the effects of inhibition. By embracing this innovative approach, researchers can analyze large numbers of sediment samples for aDNA preservation, achieving significant cost reductions of up to 70% and reducing hands-on laboratory time to one-fifth.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11339378PMC
http://dx.doi.org/10.1038/s41598-024-69741-5DOI Listing

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