Evidence map›Paper›PMID 41712658›Full record

ArticlePLoS computational biology2026

Tracking SARS-CoV-2 genomic variants in wastewater sequencing data with LolliPop.

David Dreifuss, Ivan Topolsky, Pelin Icer Baykal, Niko Beerenwinkel

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

David DreifussDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID https://orcid.org/0000-0002-5827-5387
Ivan TopolskyDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Pelin Icer BaykalDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Niko BeerenwinkelDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID https://orcid.org/0000-0002-0573-6119

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the COVID-19 pandemic, wastewater-based epidemiology has progressively taken a central role as a pathogen surveillance tool. Tracking viral loads and variant outbreaks in sewage offers advantages over clinical surveillance methods by providing estimates not biased by testing practices and enabling early detection. However, wastewater-based epidemiology poses new computational research questions that need to be solved in order for this approach to be implemented broadly and successfully. Here, we address the variant deconvolution problem, where we aim to estimate the relative abundances of genomic variants from next-generation sequencing data of a mixed wastewater sample. We introduce LolliPop, a computational method to solve the variant deconvolution problem. LolliPop is tailored to wastewater time series sequencing data and applies temporal regularization in the form of a fused ridge penalty. We show that this regularization is equivalent to kernel smoothing and that it makes abundance estimates robust to very high levels of missing data, which is common for wastewater sequencing. We use the bootstrap to produce confidence intervals, and develop analytical standard errors that can produce similar confidence intervals at a fraction of the computational cost. We demonstrate the application of our method to data from the Swiss wastewater surveillance efforts as well as on simulated data.

Identifiers

PMID41712658
PMCPMC12945317

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.