AI Article Synopsis

  • - The initial step in analyzing ancient DNA involves verifying that the DNA sequencing reads are genuinely ancient, which is done by checking for typical post-mortem damage characteristics like cytosine deamination and nicks.
  • - A new program called ngsBriggs uses a statistical method to quickly and accurately quantify post-mortem damage (PMD) in ancient DNA, improving the estimation of damage parameters compared to previous methods.
  • - ngsBriggs not only offers greater accuracy in distinguishing ancient from modern DNA for contamination control, but it is also significantly faster than other existing techniques, making it a valuable tool for researchers.

Article Abstract

One essential initial step in the analysis of ancient DNA is to authenticate that the DNA sequencing reads are actually from ancient DNA. This is done by assessing if the reads exhibit typical characteristics of post-mortem damage (PMD), including cytosine deamination and nicks. We present a novel statistical method implemented in a fast multithreaded programme, ngsBriggs that enables rapid quantification of PMD by estimation of the Briggs ancient damage model parameters (Briggs parameters). Using a multinomial model with maximum likelihood fit, ngsBriggs accurately estimates the parameters of the Briggs model, quantifying the PMD signal from single and double-stranded DNA regions. We extend the original Briggs model to capture PMD signals for contemporary sequencing platforms and show that ngsBriggs accurately estimates the Briggs parameters across a variety of contamination levels. Classification of reads into ancient or modern reads, for the purpose of decontamination, is significantly more accurate using ngsBriggs than using other methods available. Furthermore, ngsBriggs is substantially faster than other state-of-the-art methods. ngsBriggs offers a practical and accurate method for researchers seeking to authenticate ancient DNA and improve the quality of their data.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11646307PMC
http://dx.doi.org/10.1111/1755-0998.14029DOI Listing

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