ArticleBioinformatics (Oxford, England)2020
A likelihood method for estimating present-day human contamination in ancient male samples using low-depth X-chromosome data.
Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed.
- Article
- Characterization of ancient DNA preservation in copper-patinated human bone and tooth samples from Latvia.Microbiology spectrum · 2025Article
- Archaeogenomic Analysis of Nineteenth-Century Burials at Saint Mary's Basilica: An Intersectional Analysis of Religion, Race, and Migration.American journal of biological anthropology · 2025Article
- LYCEUM: learning to call copy number variants on low-coverage ancient genomes.Bioinformatics (Oxford, England) · 2025Article
- Article
- Assessing the impact of post-mortem damage and contamination on imputation performance in ancient DNA.Scientific reports · 2024Article
- hapCon: estimating contamination of ancient genomes by copying from reference haplotypes.Bioinformatics (Oxford, England) · 2022Article
- A curated dataset of modern and ancient high-coverage shotgun human genomes.Scientific data · 2021Article
- Article
- Article
- AuthentiCT: a model of ancient DNA damage to estimate the proportion of present-day DNA contamination.Genome biology · 2020Article
- ContamLD: estimation of ancient nuclear DNA contamination using breakdown of linkage disequilibrium.Genome biology · 2020Article
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Authors and funding
7 authors.
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Abstract
motivationThe presence of present-day human contaminating DNA fragments is one of the challenges defining ancient DNA (aDNA) research. This is especially relevant to the ancient human DNA field where it is difficult to distinguish endogenous molecules from human contaminants due to their genetic similarity. Recently, with the advent of high-throughput sequencing and new aDNA protocols, hundreds of ancient human genomes have become available. Contamination in those genomes has been measured with computational methods often developed specifically for these empirical studies. Consequently, some of these methods have not been implemented and tested for general use while few are aimed at low-depth nuclear data, a common feature in aDNA datasets.
resultsWe develop a new X-chromosome-based maximum likelihood method for estimating present-day human contamination in low-depth sequencing data from male individuals. We implement our method for general use, assess its performance under conditions typical of ancient human DNA research, and compare it to previous nuclear data-based methods through extensive simulations. For low-depth data, we show that existing methods can produce unusable estimates or substantially underestimate contamination. In contrast, our method provides accurate estimates for a depth of coverage as low as 0.5× on the X-chromosome when contamination is below 25%. Moreover, our method still yields meaningful estimates in very challenging situations, i.e. when the contaminant and the target come from closely related populations or with increased error rates. With a running time below 5 min, our method is applicable to large scale aDNA genomic studies. AVAILABILITY AND IMPLEMENTATION: The method is implemented in C++ and R and is available in github.com/sapfo/contaminationX and popgen.dk/angsd.
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