ArticleNAR molecular medicine2026
Evaluation of ensilication technology for ambient DNA preservation.
Article in NAR molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Ensilication preserves high-molecular weight native DNA for clinical long-read sequencing.Genome biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
24 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Current nucleic acid preservation relies on ultra-low temperature storage (-20°C to -80°C), imposing significant infrastructure, cost, and accessibility barriers that limit genomic medicine worldwide. We present a comprehensive evaluation of ensilication, a silica-based encapsulation method enabling ambient-temperature preservation of DNA without compromising sequencing fidelity. Across clinical, genomic, and biochemical analyses, ensilication maintained complete diagnostic concordance with cryogenic controls, detecting all actionable variants in FFPE tumor samples, even at low variant allele frequencies. Whole-genome sequencing revealed that frozen storage accumulated up to 65% more artifactual C>T mutations than ensilicated samples, underscoring its potential to reduce false-positive calls in oncology. Both linear and circular DNA libraries preserved structural integrity across temperatures from -80°C to 37°C. By eliminating cold-chain dependence, ensilication enables decentralized biobanking, point-of-care testing, and equitable access to precision oncology, enabling globally accessible cancer genomics. Its compatibility with emerging sequencing platforms positions ensilication as a foundational technology for next-generation diagnostics and large-scale population studies.
Identifiers
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Registered trials
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.