期刊论文详细信息
BMC Genetics
Hypothesis testing of meiotic recombination rates from population genetic data
Junming Yin1 
[1] Department of Management Information Systems, Eller College of Management, University of Arizona, Tucson 85721, USA
关键词: Hypothesis testing;    Gene conversion;    Recombination rates;   
Others  :  1085198
DOI  :  10.1186/s12863-014-0122-7
 received in 2014-05-06, accepted in 2014-10-28,  发布年份 2014
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【 摘 要 】

Background

Meiotic recombination, one of the central biological processes studied in population genetics, comes in two known forms: crossovers and gene conversions. A number of previous studies have shown that when one of these two events is nonexistent in the genealogical model, the point estimation of the corresponding recombination rate by population genetic methods tends to be inflated. Therefore, it has become necessary to obtain statistical evidence from population genetic data about whether one of the two recombination events is absent.

Results

In this paper, we formulate this problem in a hypothesis testing framework and devise a testing procedure based on the likelihood ratio test (LRT). However, because the null value (i.e., zero) lies on the boundary of the parameter space, the regularity conditions for the large‐sample approximation to the distribution of the LRT statistic do not apply. In turn, the standard chi‐squared approximation is inaccurate. To address this critical issue, we propose a parametric bootstrap procedure to obtain an approximate p‐value for the observed test statistic. Coalescent simulations are conducted to show that our approach yields accurate null p‐values that closely follow the theoretical prediction while the estimated alternative p‐values tend to concentrate closer to zero. Finally, the method is demonstrated on a real biological data set from the telomere of the X chromosome of African Drosophila melanogaster.

Conclusions

Our methodology provides a necessary complement to the existing procedures of estimating meiotic recombination rates from population genetic data.

【 授权许可】

   
2014 Yin; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Wall JD: Close look at gene conversion hot spots. Nat Genet 2004, 36(2):114-115.
  • [2]Li N, Stephens M: Modeling linkage disequilibrium and identifying recombination hotspots using single‐nucleotide polymorphism data. Genetics 2003, 165(4):2213-2233.
  • [3]Gay JC, Myers S, McVean G: Estimating meiotic gene conversion rates from population genetic data. Genetics 2007, 177(2):881-894.
  • [4]Yin J, Jordan MI, Song YS: Joint estimation of gene conversion rates and mean conversion tract lengths from population SNP data. Bioinformatics 2009, 25(12):231-239.
  • [5]Wang Y, Rannala B: Population genomic inference of recombination rates and hotspots. Proc Natl Acad Sci 2009, 106(15):6215-6219.
  • [6]Padhukasahasram B, Rannala B: Bayesian population genomic inference of crossing over and gene conversion. Genetics 2011, 189(2):607-619.
  • [7]Yin J: Computational methods for meiotic recombination inference. PhD thesis, University of California, Berkeley, Berkeley, CA, 2010.
  • [8]Kingman JFC: The coalescent. Stochastic Processes Appl 1982, 13(3):235-248.
  • [9]Wiuf C, Hein J: The coalescent with gene conversion. Genetics 2000, 155(1):451-462.
  • [10]Wiuf C: A coalescence approach to gene conversion. Theor Popul Biol 2000, 57(4):357-367.
  • [11]Song YS, Lyngsø R, Hein J: Counting all possible ancestral configurations of sample sequences in population genetics. IEEE/ACM Trans Comput Biol Bioinform 2006, 3(3):239-251.
  • [12]Rabiner L: A tutorial on HMM and selected applications in speech recognition. Proc IEEE 1989, 77(2):257-286.
  • [13]Ghahramani Z, Jordan MI: Factorial hidden markov models. Mach Learn 1997, 29:245-273.
  • [14]Hilliker AJ, Harauz G, Reaume AG, Gray M, Clark SH, Chovnick A: Meiotic gene conversion tract length distribution within the rosy locus of drosophila melanogaster. Genetics 1994, 137(4):1019-1026.
  • [15]Jeffreys AJ, May CA: Intense and highly localized gene conversion activity in human meiotic crossover hot spots. Nat Genet 2004, 36(2):151-156.
  • [16]Nocedal J, Wright SJ: Numerical Optimization . Springer, New York; 2000.
  • [17]Hudson RR: Generating samples under the Wright‐Fisher neutral model of genetic variation. Bioinformatics 2002, 18(2):337-338.
  • [18]Ferguson T: A Course in Large Sample Theory. Chapman & Hall/CRC Texts in Statistical Science . Chapman and Hall/CRC, United Kingdom; 1996.
  • [19]Efron B, Tibshirani RJ: An Introduction to the Bootstrap. Chapman & Hall/CRC Monographs on Statistics & Applied Probability . Chapman and Hall/CRC, United Kingdom; 1994.
  • [20]Langley CH, Lazzaro BP, Phillips W, Heikkinen E, Braverman JM: Linkage disequilibria and the site frequency spectra in the su(s) and su ( wa) regions of the Drosophila melanogaster X chromosome. Genetics2000, 156:1837–1852.
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