2021
DOI: 10.1101/2021.09.08.21263279
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QuaID: Enabling Earlier Detection of Recently Emerged SARS-CoV-2 Variants of Concern in Wastewater

Abstract: SARS-CoV-2 RNA shedding in stool enabled wastewater surveillance for the genetic material of the virus. With the emergence of novel variants of concern and interest it becomes increasingly important to track arrival and spread of these variants. However, most current approaches rely on the manually curated lists of mutations phenotypically associated with the variants of concern. The resulting data has many overlaps between distinct variants leading to less specific characterization of complex sample mixtures … Show more

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Cited by 9 publications
(15 citation statements)
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“…A potential explanation could be that cases are only reported once when an infection is detected whereas virus material can be found in wastewater for a longer period. This seems to be dependent on the respective virus variant as indicated earlier in the literature, where shedding patterns were found to differ between virus variants (Bertels et al, 2022; Sapoval et al, 2021; Wurtzer et al, 2022). It may be worthwhile to train a separate model (and lag) for each slope of the data to enhance coherence.…”
Section: Discussionsupporting
confidence: 67%
“…A potential explanation could be that cases are only reported once when an infection is detected whereas virus material can be found in wastewater for a longer period. This seems to be dependent on the respective virus variant as indicated earlier in the literature, where shedding patterns were found to differ between virus variants (Bertels et al, 2022; Sapoval et al, 2021; Wurtzer et al, 2022). It may be worthwhile to train a separate model (and lag) for each slope of the data to enhance coherence.…”
Section: Discussionsupporting
confidence: 67%
“…Methods for the quantification of previously described and/or de novo variants from the complex genotype mixtures in WW are being developed but not well established yet 42,[67][68][69] . Our approach to assign mutations to mutation constellations based on their individual mutation frequencies across several samples using DeViVa serves as a proof of principle and can be integrated directly with the variant definition-guided VaQuERo approach to identify emerging mutation constellations and investigate their temporal and spatial development patterns.…”
Section: Discussionmentioning
confidence: 99%
“…Tracing signature mutations, or quasi-signature mutations [44], does not allow in general for the reconstructing of full-length haplotypes of SARS-CoV-2 and thus assessing the combinations of characteristic mutations. We show that for genomic regions enriched in mutations, haplotype reconstruction based on SNP co-occurrence could be feasible, but we were mainly able to predict short haplotypes for abundant lineages.…”
Section: Discussionmentioning
confidence: 99%