HIV-phyloTSI: Subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence data
Golubchik, T.; Abeler-Dorner, L.; Hall, M.; Wymant, C.; Bonsall, D.; Macintyre-Cockett, G.; Thomson, L.; Baeten, J. M.; Celum, C. L.; Galiwango, R. M.; Kosloff, B.; Limbada, M.; Mujugira, A.; Mugo, N. R.; Gall, A.; Blanquart, F.; Bakker, M.; Bezemer, D.; Ong, S. H.; Albert, J.; Bannert, N.; Fellay, J.; Gunsenheimer-Bartmeyer, B.; Gunthard, H. F.; Kivela, P.; Kouyos, R. D.; Meyer, L.; Porter, K.; van Sighem, A.; van der Valk, M.; Berkhout, B.; Kellam, P.; Cornelissen, M.; Reiss, P.; Ayles, H.; Burns, D. N.; Fidler, S.; Grabowski, M. K.; Hayes, R.; Herbeck, J. T.; Kagaayi, J.; Kaleebu, P.; Linga
Show abstract
Estimating the time since HIV infection (TSI) at population level is essential for tracking changes in the global HIV epidemic. Most methods for determining duration of infection classify samples into recent and non-recent and are unable to give more granular TSI estimates. These binary classifications have a limited recency time window of several months, therefore requiring large sample sizes, and cannot assess the cumulative impact of an intervention. We developed a Random Forest Regression model, HIV-phyloTSI, that combines measures of within-host diversity and divergence to generate TSI estimates from viral deep-sequencing data, with no need for additional variables. HIV-phyloTSI provides a continuous measure of TSI up to 9 years, with a mean absolute error of less than 12 months overall and less than 5 months for infections with a TSI of up to a year. It performed equally well for all major HIV subtypes based on data from African and European cohorts. We demonstrate how HIV-phyloTSI can be used for incidence estimates on a population level.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Differences in HIV-1 reservoir size, landscape characteristics and decay dynamics in acute and chronic treated HIV-1 Clade C infection 94%
- Integrator complex subunit 12 knockout overcomes a transcriptional block to HIV latency reversal 93%
- Deep-sequence phylogenetics to quantify patterns of HIV transmission in the context of a universal testing and treatment trial – BCPP/ Ya Tsie trial 93%
Similar papers in this journal
- Quantifying prevalence and risk factors of HIV multiple infection in Uganda from population-based deep-sequence data 95%
- A de novo approach to inferring within-host fitness effects during untreated HIV-1 infection 94%
- HIV proviral genetic diversity, compartmentalization and inferred dynamics in lung and blood during long-term suppressive antiretroviral therapy 94%
Similar papers in this journal
- Phylogenetic inference of changes in amino acid propensities with single-position resolution 94%
- A deep learning approach to real-time HIV outbreak detection using genetic data 93%
- Learning patterns of HIV-1 co-resistance to broadly neutralizing antibodies with reduced subtype bias using multi-task learning 93%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.