Evidence map›Paper›PMID 34782917›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2022

MoG+: a database of genomic variations across three mouse subspecies for biomedical research.

Toyoyuki Takada, Kentaro Fukuta, Daiki Usuda, Tatsuya Kushida, Shinji Kondo, Shoko Kawamoto, Atsushi Yoshiki, Yuichi Obata, Asao Fujiyama, Atsushi Toyoda and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. MoG+3.0: expanded structural variant visualization and integration of genomic data from five newly analyzed mouse strains.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Mammalian genome research resources available from the National BioResource Project in Japan.Mammalian genome : official journal of the International Mammalian Genome Society · 2024
    Review
  9. Article
  10. Article
  11. 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

13 authors at 3 institutions in 1 country.

Toyoyuki TakadaIntegrated Bioresource Information Division, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan. toyoyuki.takada@riken.jp.
Kentaro FukutaCenter for Genome Informatics, Joint Support-Center for Data Science Research, Research Organization of Information and Systems, 1111 Yata, Mishima, 411-8540, Japan.
Daiki UsudaIntegrated Bioresource Information Division, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.
Tatsuya KushidaIntegrated Bioresource Information Division, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.
Shinji KondoCenter for Genome Informatics, Joint Support-Center for Data Science Research, Research Organization of Information and Systems, 1111 Yata, Mishima, 411-8540, Japan.
Shoko KawamotoGenetic Informatics Laboratory, National Institute of Genetics, 1111 Yata, Mishima, 411-8540, Japan.
Atsushi YoshikiExperimental Animal Division, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.
Yuichi ObataRIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.
Asao FujiyamaCenter for Genome Informatics, Joint Support-Center for Data Science Research, Research Organization of Information and Systems, 1111 Yata, Mishima, 411-8540, Japan.
Atsushi ToyodaAdvanced Genomics Center, National Institute of Genetics, 1111 Yata, Mishima, 411-8540, Japan.
Hideki NoguchiCenter for Genome Informatics, Joint Support-Center for Data Science Research, Research Organization of Information and Systems, 1111 Yata, Mishima, 411-8540, Japan.
Toshihiko ShiroishiRIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan. toshihiko.shiroishi@riken.jp.
Hiroshi MasuyaIntegrated Bioresource Information Division, RIKEN BioResource Research Center, 3-1-1 Koyadai, Tsukuba, Ibaraki, 305-0074, Japan. hiroshi.masuya@riken.jp.
RIKEN BioResource Research Center · JPNational Institute of Genetics · JPResearch Organization of Information and Systems · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laboratory mouse strains have mosaic genomes derived from at least three major subspecies that are distributed in Eurasia. Here, we describe genomic variations in ten inbred strains: Mus musculus musculus-derived BLG2/Ms, NJL/Ms, CHD/Ms, SWN/Ms, and KJR/Ms; M. m. domesticus-derived PGN2/Ms and BFM/Ms; M. m. castaneus-derived HMI/Ms; and JF1/Ms and MSM/Ms, which were derived from a hybrid between M. m. musculus and M. m. castaneus. These strains were established by Prof. Moriwaki in the 1980s and are collectively named the "Mishima Battery". These strains show large phenotypic variations in body size and in many physiological traits. We resequenced the genomes of the Mishima Battery strains and performed a comparative genomic analysis with dbSNP data. More than 81 million nucleotide coordinates were identified as variant sites due to the large genetic distances among the mouse subspecies; 8,062,070 new SNP sites were detected in this study, and these may underlie the large phenotypic diversity observed in the Mishima Battery. The new information was collected in a reconstructed genome database, termed MoG+ that includes new application software and viewers. MoG+ intuitively visualizes nucleotide variants in genes and intergenic regions, and amino acid substitutions across the three mouse subspecies. We report statistical data from the resequencing and comparative genomic analyses and newly collected phenotype data of the Mishima Battery, and provide a brief description of the functions of MoG+, which provides a searchable and unique data resource of the numerous genomic variations across the three mouse subspecies. The data in MoG+ will be invaluable for research into phenotype-genotype links in diverse mouse strains.

Indexed as

Databases, GeneticGenomeMice, Inbred StrainsAnimalsBiomedical ResearchGenomicsMiceNucleotidesNucleotides

Identifiers

PMID34782917
PMCPMC8913468
OpenAlexW3211957639

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.