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Content and Performance of the MiniMUGA Genotyping Array: A New Tool To Improve Rigor and Reproducibility in Mouse Research

Authors :
Martin T. Ferris
Sarah A. Schoenrock
Timothy R. Gershon
David B. Darr
Mark J. Zylka
J. Mauro Calabrese
James E. Faber
Laura G. Reinholdt
David W. Threadgill
John R. Shorter
Kathleen M. Caron
Lisa E. Gralinski
Robert S. Hagan
Glenn K. Matsushima
Yuyu Ren
Christopher M. Sassetti
Christiann H. Gaines
Bin Gu
Lori L. O'Brien
Sheryl S. Moy
Timothy A. Bell
Keegan Wardwell
Barbara J. Vilen
Terry Magnuson
Darla R. Miller
Clare M. Smith
Abraham A. Palmer
A. Wesley Burks
Fernando Pardo-Manuel de Villena
Celine L. St. Pierre
William Valdar
Rachel C. McMullan
Pablo Hock
Frank L. Conlon
Kevin C K Lloyd
Gudrun A. Brockmann
Anwica Kashfeen
Ginger D. Shaw
Steve Rockwood
Karen L. Mohlke
Matthew Blanchard
Alessandra Livraghi-Butrico
Benjamin D. Philpot
Rachel M Lynch
Scott H. Randell
J. Brennan
John Sebastian Sigmon
Vivek Kumar
Ralph S. Baric
Leonard McMillan
Mark T. Heise
Ernest G. Heimsath
Richard E. Cheney
Avani Saraswatula
Lucy H. Williams
Allison R. Rogala
Colton L. Linnertz
Caroline E. Y. Murphy
Dominic Ciavatta
Mike Kulis
Tal Kafri
Craig L. Franklin
Jason K. Whitmire
J. Charles Jennette
Maya L. Najarian
Cathleen M. Lutz
Jonathan C. Schisler
Lisa M. Tarantino
Folami Y. Ideraabdullah
Source :
Genetics: a periodical record of investigations bearing on heredity and variation, vol 216, iss 4, Genetics
Publication Year :
2020
Publisher :
eScholarship, University of California, 2020.

Abstract

The laboratory mouse is the most widely used animal model for biomedical research, due in part to its well-annotated genome, wealth of genetic resources, and the ability to precisely manipulate its genome. Despite the importance of genetics for mouse research, genetic quality control (QC) is not standardized, in part due to the lack of cost-effective, informative, and robust platforms. Genotyping arrays are standard tools for mouse research and remain an attractive alternative even in the era of high-throughput whole-genome sequencing. Here, we describe the content and performance of a new iteration of the Mouse Universal Genotyping Array (MUGA), MiniMUGA, an array-based genetic QC platform with over 11,000 probes. In addition to robust discrimination between most classical and wild-derived laboratory strains, MiniMUGA was designed to contain features not available in other platforms: (1) chromosomal sex determination, (2) discrimination between substrains from multiple commercial vendors, (3) diagnostic SNPs for popular laboratory strains, (4) detection of constructs used in genetically engineered mice, and (5) an easy-to-interpret report summarizing these results. In-depth annotation of all probes should facilitate custom analyses by individual researchers. To determine the performance of MiniMUGA, we genotyped 6899 samples from a wide variety of genetic backgrounds. The performance of MiniMUGA compares favorably with three previous iterations of the MUGA family of arrays, both in discrimination capabilities and robustness. We have generated publicly available consensus genotypes for 241 inbred strains including classical, wild-derived, and recombinant inbred lines. Here, we also report the detection of a substantial number of XO and XXY individuals across a variety of sample types, new markers that expand the utility of reduced complexity crosses to genetic backgrounds other than C57BL/6, and the robust detection of 17 genetic constructs. We provide preliminary evidence that the array can be used to identify both partial sex chromosome duplication and mosaicism, and that diagnostic SNPs can be used to determine how long inbred mice have been bred independently from the relevant main stock. We conclude that MiniMUGA is a valuable platform for genetic QC, and an important new tool to increase the rigor and reproducibility of mouse research.

Details

Database :
OpenAIRE
Journal :
Genetics: a periodical record of investigations bearing on heredity and variation, vol 216, iss 4, Genetics
Accession number :
edsair.doi.dedup.....2f021d31a7f2e88239f86551bdc6e73b