Evidence map›Paper›PMID 35474894›Full record

ArticleCell reports methods2021

Probe design for simultaneous, targeted capture of diverse metagenomic targets.

Zachery W Dickson, Dirk Hackenberger, Melanie Kuch, Art Marzok, Arinjay Banerjee, Laura Rossi, Jennifer Ann Klowak, Alison Fox-Robichaud, Karen Mossmann, Matthew S Miller and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Enrichment techniques for clinical metagenomics.Frontiers in cellular and infection microbiology · 2026
    Review
  6. Article
  7. OLTA: Optimizing bait seLection for TArgeted sequencing.Bioinformatics (Oxford, England) · 2025
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Zachery W DicksonDepartment of Biology, McMaster University, Hamilton, ON L8S 4K1, Canada.
Dirk HackenbergerDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Melanie KuchMcMaster aDNA Center, Department of Anthropology, McMaster University, Hamilton, ON L8S 4L9, Canada.
Art MarzokDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Arinjay BanerjeeMichael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Laura RossiDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Jennifer Ann KlowakDepartment of Pediatrics, McMaster University, Hamilton, ON L8S 4K1, Canada.
Alison Fox-RobichaudDepartment of Medicine, McMaster University, Hamilton, ON L8S 4K1, Canada.
Karen MossmannMichael G. DeGroote Institute for Infectious Disease Research, McMaster University, Hamilton, ON L8S 4K1, Canada.
Matthew S MillerDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Michael G SuretteDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
Geoffrey Brian GoldingDepartment of Biology, McMaster University, Hamilton, ON L8S 4K1, Canada.
Hendrik PoinarDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON L8S 4K1, Canada.
McMaster University · CAUniversity of Saskatchewan · CA

Funding

CIHR
6 · The paper itself

Abstract

The compounding challenges of low signal, high background, and uncertain targets plague many metagenomic sequencing efforts. One solution has been DNA capture, wherein probes are designed to hybridize with target sequences, enriching them in relation to their background. However, balancing probe depth with breadth of capture is challenging for diverse targets. To find this balance, we have developed the HUBDesign pipeline, which makes use of sequence homology to design probes at multiple taxonomic levels. This creates an efficient probe set capable of simultaneously and specifically capturing known and related sequences. We validated HUBDesign by generating probe sets targeting the breadth of coronavirus diversity, as well as a suite of bacterial pathogens often underlying sepsis. In separate experiments demonstrating significant, simultaneous enrichment, we captured SARS-CoV-2 and HCoV-NL63 in a human RNA background and seven bacterial strains in human blood. HUBDesign (https://github.com/zacherydickson/HUBDesign) has broad applicability wherever there are multiple organisms of interest.

Indexed as

COVID-19SARS-CoV-2BacteriaHumansMetagenomemetagenomicsnext-generation sequencingprobe designSARS-CoV-2sepsistargeted DNA capture

Identifiers

PMID35474894
PMCPMC9017208
OpenAlexW3200055919

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.