Evidence map›Paper›PMID 28827289›Full record

ArticleGenetics2017

MIP-MAP: High-Throughput Mapping of

Calvin A Mok, Vinci Au, Owen A Thompson, Mark L Edgley, Louis Gevirtzman, John Yochem, Joshua Lowry, Nadin Memar, Matthew R Wallenfang, Dominique Rasoloson and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Mutation Mapping and Identification by Whole-Genome Sequencing.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. A complement factor H homolog, heparan sulfation, and syndecan maintain inversin compartment boundaries inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Population Selection and Sequencing ofG3 (Bethesda, Md.) · 2019
    Article
  14. Article
  15. Article
  16. 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

15 authors at 8 institutions in 3 countries.

Calvin A MokDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195 mok.calvin@gmail.com.ORCID 0000-0001-7968-2857
Vinci AuDepartment of Zoology and Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.ORCID 0000-0002-3587-6200
Owen A ThompsonDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.
Mark L EdgleyDepartment of Zoology and Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.ORCID 0000-0001-9113-8862
Louis GevirtzmanDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.
John YochemInstitute of Molecular Biology, University of Oregon, Eugene, Oregon 97403.
Joshua LowryInstitute of Molecular Biology, University of Oregon, Eugene, Oregon 97403.ORCID 0000-0003-3671-469X
Nadin MemarDepartment Biology II, Biocenter, Ludwig-Maximilians-Universität München, 82152 Planneg-Martinsried, Germany.
Matthew R WallenfangDepartment of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Dominique RasolosonDepartment of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.ORCID 0000-0003-2210-1569
Bruce BowermanInstitute of Molecular Biology, University of Oregon, Eugene, Oregon 97403.ORCID 0000-0002-6479-8707
Ralf SchnabelDepartment of Developmental Genetics, Institute of Genetics, Technische Universität Braunschweig, 38106, Germany.
Geraldine SeydouxDepartment of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.ORCID 0000-0001-8257-0493
Donald G MoermanDepartment of Zoology and Michael Smith Laboratories, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Robert H WaterstonDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.ORCID 0000-0001-5956-5215
University of Washington · USUniversity of Oregon · USHoward Hughes Medical Institute · USUniversity of British Columbia · CACanada's Michael Smith Genome Sciences Centre · CAJohns Hopkins University · USLudwig-Maximilians-Universität München · DETechnische Universität Braunschweig · DE

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007348 · NICHD · UNIVERSITY OF OREGON · PI Chris Q Doe, KRYN STANKUNAS · 1989 to 2026
$6.8M
Mitotic Spindle Assembly & Function in C. elegans - Equipment SupplementR01GM049869 · NIGMS · UNIVERSITY OF OREGON · PI BOWERMAN, BRUCE A · 1994 to 2019
$6.5M
REGULATION OF GERM CELL FATE DURING EMBRYOGENESISR01HD037047 · NICHD · JOHNS HOPKINS UNIVERSITY · PI GERALDINE Catherine Joelle SEYDOUX · 1999 to 2026
$4.3M
Regulation of Germ Cell Fate During EmbryogenesisR37HD037047 · NICHD · JOHNS HOPKINS UNIVERSITY · PI SEYDOUX, GERALDINE CATHERINE JOELLE · 2016 to 2025
$3.8M
A genome-wide mutation resource for C. elegansRC2HG005921 · NHGRI · UNIVERSITY OF WASHINGTON · PI WATERSTON, ROBERT H · 2010 to 2010
$2.0M
Systems Analysis of Conditional C. elegans Mutants with Late Embryonic DefectsR01GM114053 · NIGMS · UNIVERSITY OF OREGON · PI BOWERMAN, BRUCE A · 2015 to 2018
$1.3M
High throughput methods for Synthetic Genetic Array Analysis in C. elegansR21HG007201 · NHGRI · UNIVERSITY OF WASHINGTON · PI WATERSTON, ROBERT H · 2013 to 2014
$425k
CIHR MFE-135408NHGRI NIH HHS R21 HG007201NHGRI NIH HHS RC2 HG005921NICHD NIH HHS R01 HD037047NICHD NIH HHS R37 HD037047NICHD NIH HHS T32 HD007348NIGMS NIH HHS R01 GM049869NIGMS NIH HHS R01 GM114053NIH HHS P40 OD010440
6 · The paper itself

Abstract

Mutants remain a powerful means for dissecting gene function in model organisms such as

Indexed as

MutationAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromosome MappingChromosomesThermotoleranceWhole Genome SequencingCaenorhabditis elegans ProteinsCaenorhabditis elegansgenetic mappingmassively multiplex sequencingmolecular inversion probestemperature-sensitive mutations

Identifiers

PMID28827289
PMCPMC5629315
OpenAlexW2952583633

What OpenQuestion holds

Textmetadata
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.