Evidence map›Paper›PMID 39399973›Full record

ArticleGigaScience2024

MISIP: a data standard for the reuse and reproducibility of any stable isotope probing-derived nucleic acid sequence and experiment.

Abigayle Simpson, Elisha M Wood-Charlson, Montana Smith, Benjamin J Koch, Kathleen Beilsmith, Jeffrey A Kimbrel, Matthew Kellom, Christopher I Hunter, Ramona L Walls, Lynn M Schriml and 1 more

Abstract read
In one paragraph

Article in GigaScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Article
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

11 authors.

Abigayle SimpsonDepartment of Agronomy, Lilly Hall of Life Sciences, Purdue University, West Lafayette, IN 47907, USA.ORCID 0000-0003-1714-6535
Elisha M Wood-CharlsonEnvironmental Genomics and Systems Biology Division, E.O. Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.ORCID 0000-0001-9557-7715
Montana SmithEarth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, WA 99354, USA.ORCID 0000-0002-8683-0050
Benjamin J KochCenter for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ 86011, USA.
Kathleen BeilsmithData Science and Learning Division, Argonne National Laboratory, Lemont, IL 60439, USA.ORCID 0000-0003-2778-299X
Jeffrey A KimbrelPhysical and Life Sciences Directorate, Lawrence Livermore National Laboratory, Livermore, CA 94550, USA.ORCID 0000-0001-7213-9392
Matthew KellomDOE Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.ORCID 0000-0002-8310-7078
Christopher I HunterGigaScience, BGI-Hong Kong, Hong Kong.ORCID 0000-0002-1335-0881
Ramona L WallsData Collaboration Center, Critical Path Institute, Tucson, AZ 85718, USA.ORCID 0000-0001-8815-0078
Lynn M SchrimlDepartment of Epidemiology and Public Health, University of Maryland School of Medicine, Institute for Genome Sciences, Baltimore, MD 21201, USA.ORCID 0000-0001-8910-9851
Roland C WilhelmDepartment of Agronomy, Lilly Hall of Life Sciences, Purdue University, West Lafayette, IN 47907, USA.ORCID 0000-0003-1170-1753

Funding

Lawrence Berkeley National LaboratoryPurdue UniversityUSDA IND90024429
6 · The paper itself

Abstract

DNA/RNA-stable isotope probing (SIP) is a powerful tool to link in situ microbial activity to sequencing data. Every SIP dataset captures distinct information about microbial community metabolism, process rates, and population dynamics, offering valuable insights for a wide range of research questions. Data reuse maximizes the information derived from the labor and resource-intensive SIP approaches. Yet, a review of publicly available SIP sequencing metadata showed that critical information necessary for reproducibility and reuse was often missing. Here, we outline the Minimum Information for any Stable Isotope Probing Sequence (MISIP) according to the Minimum Information for any (x) Sequence (MIxS) framework and include examples of MISIP reporting for common SIP experiments. Our objectives are to expand the capacity of MIxS to accommodate SIP-specific metadata and guide SIP users in metadata collection when planning and reporting an experiment. The MISIP standard requires 5 metadata fields-isotope, isotopolog, isotopolog label, labeling approach, and gradient position-and recommends several fields that represent best practices in acquiring and reporting SIP sequencing data (e.g., gradient density and nucleic acid amount). The standard is intended to be used in concert with other MIxS checklists to comprehensively describe the origin of sequence data, such as for marker genes (MISIP-MIMARKS) or metagenomes (MISIP-MIMS), in combination with metadata required by an environmental extension (e.g., soil). The adoption of the proposed data standard will improve the reuse of any sequence derived from a SIP experiment and, by extension, deepen understanding of in situ biogeochemical processes and microbial ecology.

Indexed as

Isotope LabelingMetadataMetagenomeMetagenomicsMicrobiotaReproducibility of ResultsSequence Analysis, DNAampliconmetagenomemetatranscriptomemicrobial ecologyMIMARKSMIMSminimum information standardMIxSstable isotope probing

Identifiers

PMID39399973
PMCPMC11471955

What OpenQuestion holds

Textmetadata
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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.