Detection and integration of genotyping errors in statistical genetics.
By E. Sobel, Jeanette C. Papp, Kenneth L. Lange. American Journal of Human Genetics, 2002
373 citations recorded by the source corpus.
Subfields: Genetics
View Paper: https://www.semanticscholar.org/paper/d653bf943aa3ace7f046dd6ca687bfee988ce00d
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In Genetics
- P. Taberlet
- E. Bellemain
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- F. Pompanon
- P. B. Eidesen
- Aurélie Bonin
- Jean Bousquet
- Peter J. Nürnberg
Citations in the corpus
- HomozygosityMapper—an interactive approach to homozygosity mapping (2009, methodology): “Especially for SNP markers, owing to their low informativity and hence the usually small number of informative meioses, this is mostly carried out with multipoint linkage analysis with software such as GENEHUNTER (4) or derivatives (5,6), Allegro (7), SIMWALK2 (8) or Merlin (9) under a recessive dis”
- Economic Importance, Breeding Objectives and Achievements (2011, background): “Various workers have since dealt with this issue (Sobel et al. 2002) and new SNP genotyping methods have shown to be highly accurate, with error rate below 1% (Pavy et al.”
- Revising how the computer program cervus accommodates genotyping error increases success in paternity assignment (2007, neutral): “2000; Sobel et al .”
- Close-Kin Mark-Recapture (2016, methodology): “Thompson (1975) used (5.2) to develop a general likelihood framework for estimating κ and inferring kij of a pair of individuals.”
- How to track and assess genotyping errors in population genetics studies (2004, background): “Unfortunately, as a logical corollary of this major breakthrough, the number of genotyping errors is expected to increase with the size of data sets (Sobel et al. 2002) and those errors often go undetected because they are generally”
- Genotyping errors: causes, consequences and solutions (2005, methodology): “It is also valuable to use methods that calculate the likelihood of obtained genotypes or pedigrees using a model of error occurrence, such as a uniform or empirical distribution of error”