<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Teboul L</submitter><funding>Agence Nationale de la Recherche</funding><funding>Agence Nationale de la Recherche (French National Research Agency)</funding><funding>NIH HHS</funding><pagination>5574</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11220107</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>The biomedical research community addresses reproducibility challenges in animal studies through standardized nomenclature, improved experimental design, transparent reporting, data sharing, and centralized repositories. The ARRIVE guidelines outline documentation standards for laboratory animals in experiments, but genetic information is often incomplete. To remedy this, we propose the Laboratory Animal Genetic Reporting (LAG-R) framework. LAG-R aims to document animals' genetic makeup in scientific publications, providing essential details for replication and appropriate model use. While verifying complete genetic compositions may be impractical, better reporting and validation efforts enhance reliability of research. LAG-R standardization will bolster reproducibility, peer review, and overall scientific rigor.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Improving laboratory animal genetic reporting: LAG-R guidelines.</pubmed_title><pmcid>PMC11220107</pmcid><funding_grant_id>ANR-10-INBS-07</funding_grant_id><funding_grant_id>U42 OD010921</funding_grant_id><pubmed_authors>Bunton-Stasyshyn R</pubmed_authors><pubmed_authors>Dobbie M</pubmed_authors><pubmed_authors>Pardo Manuel de Villena F</pubmed_authors><pubmed_authors>Wells S</pubmed_authors><pubmed_authors>Wang CK</pubmed_authors><pubmed_authors>Warming S</pubmed_authors><pubmed_authors>Heaney J</pubmed_authors><pubmed_authors>Pavlovic G</pubmed_authors><pubmed_authors>Mann GJ</pubmed_authors><pubmed_authors>Haffner R</pubmed_authors><pubmed_authors>Arkell RM</pubmed_authors><pubmed_authors>Seong JK</pubmed_authors><pubmed_authors>Asian Mouse Mutagenesis Resource Association</pubmed_authors><pubmed_authors>Amos-Landgraf J</pubmed_authors><pubmed_authors>Mutant Mouse Resource and Research Centers</pubmed_authors><pubmed_authors>Fuchtbauer EM</pubmed_authors><pubmed_authors>Golzio C</pubmed_authors><pubmed_authors>Marvel J</pubmed_authors><pubmed_authors>Kueh AJ</pubmed_authors><pubmed_authors>Franklin CL</pubmed_authors><pubmed_authors>International Society for Transgenic Technologies</pubmed_authors><pubmed_authors>Phenomics Australia</pubmed_authors><pubmed_authors>Magnuson TR</pubmed_authors><pubmed_authors>Lutz CC</pubmed_authors><pubmed_authors>Pailhoux E</pubmed_authors><pubmed_authors>Peterson K</pubmed_authors><pubmed_authors>Whitelaw CB</pubmed_authors><pubmed_authors>Murray SA</pubmed_authors><pubmed_authors>International Mouse Phenotyping Consortium</pubmed_authors><pubmed_authors>Thomas PQ</pubmed_authors><pubmed_authors>CELPHEDIA infrastructure</pubmed_authors><pubmed_authors>Gao X</pubmed_authors><pubmed_authors>Lloyd KCK</pubmed_authors><pubmed_authors>RRRC- Rat Resource and Research Center</pubmed_authors><pubmed_authors>Chin HJ</pubmed_authors><pubmed_authors>Crispo M</pubmed_authors><pubmed_authors>Bryda E</pubmed_authors><pubmed_authors>Korf IF</pubmed_authors><pubmed_authors>Montoliu L</pubmed_authors><pubmed_authors>Vilotte JL</pubmed_authors><pubmed_authors>Hrabe de Angelis M</pubmed_authors><pubmed_authors>Nam KH</pubmed_authors><pubmed_authors>Birling MC</pubmed_authors><pubmed_authors>Smith C</pubmed_authors><pubmed_authors>Teboul L</pubmed_authors><pubmed_authors>Reinholdt L</pubmed_authors><pubmed_authors>Shiroishi T</pubmed_authors><pubmed_authors>Tinsley L</pubmed_authors><pubmed_authors>Herault Y</pubmed_authors><pubmed_authors>Nutter LMJ</pubmed_authors><pubmed_authors>INFRAFRONTIER consortium</pubmed_authors><pubmed_authors>Delerue F</pubmed_authors><pubmed_authors>Yoshiki A</pubmed_authors><pubmed_authors>International Mammalian Genome Society</pubmed_authors><pubmed_authors>Takeo T</pubmed_authors><pubmed_authors>Sedlacek R</pubmed_authors><pubmed_authors>Benavides FJ</pubmed_authors><pubmed_authors>Brown SDM</pubmed_authors><pubmed_authors>Zarubica A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Improving laboratory animal genetic reporting: LAG-R guidelines.</name><description>The biomedical research community addresses reproducibility challenges in animal studies through standardized nomenclature, improved experimental design, transparent reporting, data sharing, and centralized repositories. The ARRIVE guidelines outline documentation standards for laboratory animals in experiments, but genetic information is often incomplete. To remedy this, we propose the Laboratory Animal Genetic Reporting (LAG-R) framework. LAG-R aims to document animals' genetic makeup in scientific publications, providing essential details for replication and appropriate model use. While verifying complete genetic compositions may be impractical, better reporting and validation efforts enhance reliability of research. LAG-R standardization will bolster reproducibility, peer review, and overall scientific rigor.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-22T12:03:29.372Z</modification><creation>2025-04-06T00:14:18.96Z</creation></dates><accession>S-EPMC11220107</accession><cross_references><pubmed>38956430</pubmed><doi>10.1038/s41467-024-49439-y</doi></cross_references></HashMap>