Source:http://linkedlifedata.com/resource/pubmed/id/20923982
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-12-15
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pubmed:abstractText |
Phenovariance may be obscured when genetic mapping is performed using highly divergent strains, and closely similar strains are preferred if adequate marker density can be established. We sequenced the C57BL/10J mouse genome using the Applied Biosystems SOLiD platform and here describe a genome-wide panel of informative markers that permits the mapping of mutations induced on the closely related C57BL/6J background by outcrossing to C57BL/10J, and backcrossing or intercrossing. The panel consists of 127 single nucleotide polymorphisms validated by capillary sequencing: 124 spaced at ?20-Mb intervals across the 19 autosomes, and three markers on the X chromosome. We determined the genetic relationship between four C57BL-derived substrains and used the panel to map two N-ethyl-N-nitrosourea (ENU)-induced mutations responsible for visible phenotypes in C57BL/6J mice through bulk segregation analysis. Capillary sequencing, with computation of relative chromatogram peak heights, was used to determine the proportion of alleles from each strain at each marker.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1943-2631
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pubmed:author |
pubmed-author:BeutlerBruceB,
pubmed-author:DayJ OJO,
pubmed-author:GoodnowChristopher CCC,
pubmed-author:KoziolJamesJ,
pubmed-author:LüZ BZB,
pubmed-author:La VineDianthaD,
pubmed-author:LeivaGabrielG,
pubmed-author:MorescoEva Marie YEM,
pubmed-author:RossCharlesC,
pubmed-author:VidalSilvia MSM,
pubmed-author:WhittleBelindaB,
pubmed-author:WiltshireSeanS,
pubmed-author:WonSungyongS,
pubmed-author:YowMM
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pubmed:issnType |
Electronic
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pubmed:volume |
186
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1139-46
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pubmed:dateRevised |
2011-10-16
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pubmed:meshHeading |
pubmed-meshheading:20923982-Alleles,
pubmed-meshheading:20923982-Animals,
pubmed-meshheading:20923982-Chromosomes,
pubmed-meshheading:20923982-Genetic Markers,
pubmed-meshheading:20923982-Genome,
pubmed-meshheading:20923982-Genomics,
pubmed-meshheading:20923982-Mice,
pubmed-meshheading:20923982-Mice, Inbred Strains,
pubmed-meshheading:20923982-Mutagenesis,
pubmed-meshheading:20923982-Mutation,
pubmed-meshheading:20923982-Phenotype,
pubmed-meshheading:20923982-Polymorphism, Single Nucleotide,
pubmed-meshheading:20923982-Sequence Analysis, DNA,
pubmed-meshheading:20923982-Species Specificity,
pubmed-meshheading:20923982-X Chromosome
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pubmed:year |
2010
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pubmed:articleTitle |
Bulk segregation mapping of mutations in closely related strains of mice.
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pubmed:affiliation |
Department of Genetics, The Scripps Research Institute, La Jolla, California 92037, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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