ArticleJournal of applied genetics2020
The application of deep learning for the classification of correct and incorrect SNP genotypes from whole-genome DNA sequencing pipelines.
Article in Journal of applied genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Exploring the impact of sequence context on errors in SNP genotype calling with whole genome sequencing data using AI-based autoencoder approach.NAR genomics and bioinformatics · 2024Article
- Harnessing deep learning for SNP-based disease prediction in genomics.International journal of information technology : an official journal of Bharati Vidyapeeth's Institute of Computer Applications and Management · 2024Article
- A review of deep learning applications in human genomics using next-generation sequencing data.Human genomics · 2022Review
- Concat_CNN: A Model to Detect COVID-19 from Chest X-ray Images with Deep Learning.SN computer science · 2022Article
Corrections and comments
- Erratum issued
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A downside of next-generation sequencing technology is the high technical error rate. We built a tool, which uses array-based genotype information to classify next-generation sequencing-based SNPs into the correct and the incorrect calls. The deep learning algorithms were implemented via Keras. Several algorithms were tested: (i) the basic, naïve algorithm, (ii) the naïve algorithm modified by pre-imposing different weights on incorrect and correct SNP class in calculating the loss metric and (iii)-(v) the naïve algorithm modified by random re-sampling (with replacement) of the incorrect SNPs to match 30%/60%/100% of the number of correct SNPs. The training data set was composed of data from three bulls and consisted of 2,227,995 correct (97.94%) and 46,920 incorrect SNPs, while the validation data set consisted of data from one bull with 749,506 correct (98.05%) and 14,908 incorrect SNPs. The results showed that for a rare event classification problem, like incorrect SNP detection in NGS data, the most parsimonious naïve model and a model with the weighting of SNP classes provided the best results for the classification of the validation data set. Both classified 19% of truly incorrect SNPs as incorrect and 99% of truly correct SNPs as correct and resulted in the F1 score of 0.21 - the highest among the compared algorithms. We conclude the basic models were less adapted to the specificity of a training data set and thus resulted in better classification of the independent, validation data set, than the other tested models.
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