ArticleBMC bioinformatics2013
Comparing a few SNP calling algorithms using low-coverage sequencing data.
Article in BMC bioinformatics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.
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Who cites it
66 citing papers in PubMed.
- Fifteen Years of the Genome Analysis Toolkit as the De Facto Standard in Short-Read Variant Calling.International journal of molecular sciences · 2026Review
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- Pairwise comparative analysis of six haplotype assembly methods based on users' experience.BMC genomic data · 2023Article
- Evaluation of Different SNP Analysis Software and Optimal Mining Process in Tree Species.Life (Basel, Switzerland) · 2023Article
- Benchmarking of Nanopore R10.4 and R9.4.1 flow cells in single-cell whole-genome amplification and whole-genome shotgun sequencing.Computational and structural biotechnology journal · 2023Article
- Accuracy benchmark of the GeneMind GenoLab M sequencing platform for WGS and WES analysis.BMC genomics · 2022Article
- Genome-Wide Association Study of Body Weight Trait in Yaks.Animals : an open access journal from MDPI · 2022Article
- The evaluation of Bcftools mpileup and GATK HaplotypeCaller for variant calling in non-human species.Scientific reports · 2022Article
- High-throughput estimation of allele frequencies using combined pooled-population sequencing and haplotype-based data processing.Plant methods · 2022Article
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- Performance evaluation of pipelines for mapping, variant calling and interval padding, for the analysis of NGS germline panels.BMC bioinformatics · 2021Article
- Estimating sequencing error rates using families.BioData mining · 2021Article
- One is not enough: On the effects of reference genome for the mapping and subsequent analyses of short-reads.PLoS computational biology · 2021Article
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- High-Throughput Genotyping Technologies in Plant Taxonomy.Methods in molecular biology (Clifton, N.J.) · 2021Article
- Accuracy and efficiency of germline variant calling pipelines for human genome data.Scientific reports · 2020Article
- Evaluation of variant calling tools for large plant genome re-sequencing.BMC bioinformatics · 2020Article
- Versatile simulations of admixture and accurate local ancestry inference with mixnmatch and ancestryinfer.Molecular ecology resources · 2020Article
- Next-Generation Sequencing Analysis of ctDNA for the Detection of Glioma and Metastatic Brain Tumors in Adults.Frontiers in neurology · 2020Article
- Article
6 more citing papers are in PubMed but not listed here.
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMany Single Nucleotide Polymorphism (SNP) calling programs have been developed to identify Single Nucleotide Variations (SNVs) in next-generation sequencing (NGS) data. However, low sequencing coverage presents challenges to accurate SNV identification, especially in single-sample data. Moreover, commonly used SNP calling programs usually include several metrics in their output files for each potential SNP. These metrics are highly correlated in complex patterns, making it extremely difficult to select SNPs for further experimental validations.
resultsTo explore solutions to the above challenges, we compare the performance of four SNP calling algorithm, SOAPsnp, Atlas-SNP2, SAMtools, and GATK, in a low-coverage single-sample sequencing dataset. Without any post-output filtering, SOAPsnp calls more SNVs than the other programs since it has fewer internal filtering criteria. Atlas-SNP2 has stringent internal filtering criteria; thus it reports the least number of SNVs. The numbers of SNVs called by GATK and SAMtools fall between SOAPsnp and Atlas-SNP2. Moreover, we explore the values of key metrics related to SNVs' quality in each algorithm and use them as post-output filtering criteria to filter out low quality SNVs. Under different coverage cutoff values, we compare four algorithms and calculate the empirical positive calling rate and sensitivity. Our results show that: 1) the overall agreement of the four calling algorithms is low, especially in non-dbSNPs; 2) the agreement of the four algorithms is similar when using different coverage cutoffs, except that the non-dbSNPs agreement level tends to increase slightly with increasing coverage; 3) SOAPsnp, SAMtools, and GATK have a higher empirical calling rate for dbSNPs compared to non-dbSNPs; and 4) overall, GATK and Atlas-SNP2 have a relatively higher positive calling rate and sensitivity, but GATK calls more SNVs.
conclusionsOur results show that the agreement between different calling algorithms is relatively low. Thus, more caution should be used in choosing algorithms, setting filtering parameters, and designing validation studies. For reliable SNV calling results, we recommend that users employ more than one algorithm and use metrics related to calling quality and coverage as filtering criteria.
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