Influence of sequencing depth on the fidelity and sensitivity of 1%-5% low-frequency mutation detection and recommendation for standardization of sequencing depth
Zhe LiuiD, Weijin QiuiD, Shujin Fu, Xia ZhaoiD, Jun XiaiD, Chunyu GengiD, Youqian Yu, Ziling LiiD, Mingzhu LiiD, Hui JiangiD, Fang CheniD
Abstract
Sequencing depth has always played an important role in the accurate detection of low-frequency mutations. The increase of sequencing depth and the reasonable setting of threshold can maximize the probability of true positive mutation, or sensitivity. Here, we found that when the threshold was set as a fixed number of positive mutated reads, the probability of both true and false-positive mutations increased with depth. However, When the number of positive mutated reads increased in an equal proportion with depth (the threshold was transformed from a fixed number to a fixed percentage of mutated reads), the true positive probability still increased while false positive probability decreased. Through binomial distribution simulation and experimental test, it is found that the "fidelity" of detected-VAFs is the cause of this phenomenon. Firstly, we used the binomial distribution to construct a model that can easily calculate the relationship between sequencing depth and probability of true positive (or false positive), which can standardize the minimum sequencing depth for different low-frequency mutation detection. Then, the effect of sequencing depth on the fidelity of NA12878 with 3% mutation frequency and circulating tumor DNA (ctDNA of 1%, 3% and 5%) showed that the increase of sequencing depth reduced the fluctuation range of detected-VAFs around the expected VAFs, that is, the fidelity was improved. Finally, based on our experiment result, the consistency of single-nucleotide variants (SNVs) between paired FF and FFPE samples of mice increased with increasing depth, suggesting that increasing depth can improve the precision and sensitivity of low-frequency mutations. HighlightsThe normalized relationship between sequencing depth and the probability of true positive mutation (sensitivity) is established based on binomial distribution. The probability of true positive increases and the probability of false positive decreases when the number of positive mutated reads increases (threshold) in an equal proportion with depth. Detected-VAFs fluctuates regularly around expected-VAFs. The amplitude of detected-VAFs fluctuation decreases with sequencing depth and the "fidelity" increases. The increase of "fidelity" leads to a higher degree of differentiation between true and false positive mutations, which ultimately increases the true positive probability and decreases the false positive probability.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Read depth correction for somatic mutations
Jordan Anaya, Alexander Spyridon Baras·bioRxiv·Feb 16, 2022
- Accurate detection of low-level somatic mutations with technical replication for next-generation sequencing
Junho Kim, Dachan Kim, … Sangwoo Kim·bioRxiv·Aug 23, 2017
- Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data
Yoo-Jin Jiny Ha, Dominika Maziec, … Peter J. Park·bioRxiv·Oct 13, 2025
- MAESTRO affords 'breadth and depth' for mutation testing
Gregory Gydush, Erica Nguyen, … Viktor A. Adalsteinsson·bioRxiv·Jan 22, 2021
- Detecting and Quantitating Low Fraction DNA Variants with Low-Depth Sequencing
P. Song, S. X. Chen, … D. Y. Zhang·bioRxiv·Apr 26, 2020
- MERIT: a Mutation Error Rate Identification Toolkit for Ultra-deep Sequencing Applications
Mohammad Hadigol, Hossein Khiabanian·BMC BioinformaticsPeer-reviewed·Jun 8, 2018