A comparative analysis dataset for improving genuine SNP identification in ancient maize aDNA
1Department of Plant Biology, Michigan State University, East Lansing, MI 48824, USA.
Data in Brief
|March 26, 2026
Summary
This study re-analyzed ancient maize DNA (aDNA) data to improve single nucleotide polymorphism (SNP) discovery. It evaluated different methods for handling post-mortem damage (PMD) and analysis pipelines, offering insights for future aDNA research.
Area of Science:
- Ancient DNA (aDNA) research
- Paleogenomics
- Crop domestication studies
Background:
- Maize (Zea mays) aDNA is crucial for understanding its domestication, evolution, and gene flow.
- Accurate single nucleotide polymorphism (SNP) discovery in aDNA requires addressing post-mortem damage (PMD) and selecting appropriate analytical tools and read depth.
- Standardized methods for aDNA analysis in maize are currently lacking.
Purpose of the Study:
- To re-analyze existing ancient maize DNA datasets using different pipelines and criteria.
- To evaluate the impact of various post-mortem damage (PMD) correction methods and read depth settings on single nucleotide polymorphism (SNP) discovery.
- To provide a valuable resource and guidance for improving the quality of ancient maize DNA analyses.
Main Methods:
- Re-analysis of previously published ancient maize DNA data.
- Application of two distinct post-mortem damage (PMD) correction approaches: Rm5nt and NoChange.
- Processing of data using three different analysis tools: GATK, angsd, and pileupCaller.
- Evaluation under three read depth criteria: 2X, 5X, and 10X.
Main Results:
- Different analytical pipelines and read depth criteria significantly impact single nucleotide polymorphism (SNP) calls in ancient maize DNA.
- The choice of post-mortem damage (PMD) handling strategy influences the reliability of SNP discovery.
- The re-analyzed dataset serves as a benchmark for assessing analytical approaches in ancient maize genomics.
Conclusions:
- Standardized approaches are needed for robust ancient maize DNA analysis.
- Careful selection of analytical pipelines, PMD correction methods, and read depth is critical for accurate SNP discovery.
- This study offers a foundation for enhancing the quality and comparability of future ancient maize aDNA research.
Related Concept Videos
Comparing Copy Number Variations and SNPs
19.2K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
19.2K
Single Nucleotide Polymorphisms-SNPs
19.8K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
19.8K
Evolutionary Relationships through Genome Comparisons
7.2K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
7.2K
Genome-wide Association Studies-GWAS
16.6K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
16.6K


