4.5 Article

Library preparation method and DNA source influence endogenous DNA recovery from 100-year-old avian museum specimens

期刊

ECOLOGY AND EVOLUTION
卷 13, 期 8, 页码 -

出版社

WILEY
DOI: 10.1002/ece3.10407

关键词

historical DNA; library preparation; museomics; natural history collections; shotgun sequencing

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This study aims to identify the most efficient method and DNA source for collecting whole genome sequencing (WGS) data from avian museum specimens. The results show that the single-stranded DNA (ssDNA) multi-tube method can achieve higher endogenous DNA content, average read length, and sequencing efficiency compared to other tested methods. In addition, a predigestion step can further reduce exogenous DNA. These findings have the potential to significantly increase WGS coverage of historical DNA from bird specimens.
Museum specimens collected prior to cryogenic tissue storage are increasingly being used as genetic resources, and though high-throughput sequencing is becoming more cost-efficient, whole genome sequencing (WGS) of historical DNA (hDNA) remains inefficient and costly due to its short fragment sizes and high loads of exogenous DNA, among other factors. It is also unclear how sequencing efficiency is influenced by DNA sources. We aimed to identify the most efficient method and DNA source for collecting WGS data from avian museum specimens. We analyzed low-coverage WGS from 60 DNA libraries prepared from four American Robin (Turdus migratorius) and four Abyssinian Thrush (Turdus abyssinicus) specimens collected in the 1920s. We compared DNA source (toepad versus incision-line skin clip) and three library preparation methods: (1) double-stranded DNA (dsDNA), single tube (KAPA); (2) single-stranded DNA (ssDNA), multi-tube (IDT); and (3) ssDNA, single tube (Claret Bioscience). We found that the ssDNA, multi-tube method resulted in significantly greater endogenous DNA content, average read length, and sequencing efficiency than the other tested methods. We also tested whether a predigestion step reduced exogenous DNA in libraries from one specimen per species and found promising results that warrant further study. The similar to 10% increase in average sequencing efficiency of the best-performing method over a commonly implemented dsDNA library preparation method has the potential to significantly increase WGS coverage of hDNA from bird specimens. Future work should evaluate the threshold for specimen age at which these results hold and how the combination of library preparation method and DNA source influence WGS in other taxa.

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