Evidence map›Paper›PMID 38788219›Full record

ArticleBioinformatics (Oxford, England)2024

SWGTS-a platform for stream-based host DNA depletion.

Philipp Spohr, Max Ried, Laura Kühle, Alexander Dilthey

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Philipp SpohrAlgorithmic Bioinformatics, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0000-0002-6039-377X
Max RiedAlgorithmic Bioinformatics, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0000-0003-1910-6131
Laura KühleAlgorithmic Bioinformatics, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0009-0000-3581-0677
Alexander DiltheyCenter for Digital Medicine, Düsseldorf, 40225, Germany.ORCID 0000-0002-6394-4581

Funding

German Federal Ministry of Education and Research
6 · The paper itself

Abstract

motivationMicrobial sequencing data from clinical samples is often contaminated with human sequences, which have to be removed prior to sharing. Existing methods for human read removal, however, are applicable only after the target dataset has been retrieved in its entirety, putting the recipient at least temporarily in control of a potentially identifiable genetic dataset with potential implications under regulatory frameworks such as the GDPR. In some instances, the ability to carry out stream-based host depletion as part of the data transfer process may be preferable.

resultsWe present SWGTS, a client-server application for the transfer and stream-based host depletion of sequencing reads. SWGTS enforces a robust upper bound on the maximum amount of human genetic data from any one client held in memory at any point in time by storing all incoming sequencing data in a limited-size, client-specific intermediate processing buffer, and by throttling the rate of incoming data if it exceeds the speed of host depletion carried out on the SWGTS server in the background. SWGTS exposes a HTTP-REST interface, is implemented using docker-compose, Redis and traefik, and requires less than 8 Gb of RAM for deployment. We demonstrate high filtering accuracy of SWGTS; incoming data transfer rates of up to 1.65 megabases per second in a conservative configuration; and mitigation of re-identification risks by the ability to limit the number of SNPs present on a popular population-scale genotyping array covered by reads in the SWGTS buffer to a low user-defined number, such as 10 or 100. AVAILABILITY AND IMPLEMENTATION: SWGTS is available on GitHub: https://github.com/AlBi-HHU/swgts (https://doi.org/10.5281/zenodo.10891052). The repository also contains a jupyter notebook that can be used to reproduce all the benchmarks used in this article. All datasets used for benchmarking are publicly available.

Indexed as

Sequence Analysis, DNASoftwareDNAHigh-Throughput Nucleotide SequencingHumansDNA

Identifiers

PMID38788219
PMCPMC11167210

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.