vipR: variant identification in pooled DNA using R. Results: Our method vipR uses data from multiple DNA pools in order to compensate for differences in sequencing error rates along the sequenced region. More precisely, instead of aiming at discriminating sequence variants from sequencing errors, vipR identifies sequence positions that exhibit significantly different minor allele frequencies in at least two DNA pools using the Skellam distribution. The performance of vipR was compared with three other models on data from a targeted resequencing study of the TMEM132D locus in 600 individuals distributed over four DNA pools. Performance of the methods was computed on SNPs that were also genotyped individually using a MALDI-TOF technique. On a set of 82 sequence variants, vipR achieved an average sensitivity of 0.80 at an average specificity of 0.92, thus outperforming the reference methods by at least 0.17 in specificity at comparable sensitivity. Availability: The code of vipR is freely available via: http://sourceforge.net/projects/htsvipr/
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References in zbMATH (referenced in 2 articles )
Showing results 1 to 2 of 2.
- Gan, H. L.; Kolaczyk, Eric D.: Approximation of the difference of two Poisson-like counts by Skellam (2018)
- Zhao, Zhigen; Wang, Wei; Wei, Zhi: An empirical Bayes testing procedure for detecting variants in analysis of next generation sequencing data (2013)