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Multifactor dimensionality reduction (MDR) is a statistical approach, also used in machine learning automatic approaches, [1] for detecting and characterizing combinations of attributes or independent variables that interact to influence a dependent or class variable. [2] [3] [4] [5] [6] [7] [8] MDR was designed specifically to identify nonadditive interactions among discrete variables that influence a binary outcome and is considered a nonparametric and model-free alternative to traditional statistical methods such as logistic regression.

The basis of the MDR method is a constructive induction or feature engineering algorithm that converts two or more variables or attributes to a single attribute. [9] This process of constructing a new attribute changes the representation space of the data. [10] The end goal is to create or discover a representation that facilitates the detection of nonlinear or nonadditive interactions among the attributes such that prediction of the class variable is improved over that of the original representation of the data.

Illustrative example

Consider the following simple example using the exclusive OR (XOR) function. XOR is a logical operator that is commonly used in data mining and machine learning as an example of a function that is not linearly separable. The table below represents a simple dataset where the relationship between the attributes (X1 and X2) and the class variable (Y) is defined by the XOR function such that Y = X1 XOR X2.

Table 1

X1 X2 Y
0 0 0
0 1 1
1 0 1
1 1 0

A machine learning algorithm would need to discover or approximate the XOR function in order to accurately predict Y using information about X1 and X2. An alternative strategy would be to first change the representation of the data using constructive induction to facilitate predictive modeling. The MDR algorithm would change the representation of the data (X1 and X2) in the following manner. MDR starts by selecting two attributes. In this simple example, X1 and X2 are selected. Each combination of values for X1 and X2 are examined and the number of times Y=1 and/or Y=0 is counted. In this simple example, Y=1 occurs zero times and Y=0 occurs once for the combination of X1=0 and X2=0. With MDR, the ratio of these counts is computed and compared to a fixed threshold. Here, the ratio of counts is 0/1 which is less than our fixed threshold of 1. Since 0/1 < 1 we encode a new attribute (Z) as a 0. When the ratio is greater than one we encode Z as a 1. This process is repeated for all unique combinations of values for X1 and X2. Table 2 illustrates our new transformation of the data.

Table 2

Z Y
0 0
1 1
1 1
0 0

The machine learning algorithm now has much less work to do to find a good predictive function. In fact, in this very simple example, the function Y = Z has a classification accuracy of 1. A nice feature of constructive induction methods such as MDR is the ability to use any data mining or machine learning method to analyze the new representation of the data. Decision trees, neural networks, or a naive Bayes classifier could be used in combination with measures of model quality such as balanced accuracy [11] [12] and mutual information. [13]

Machine learning with MDR

As illustrated above, the basic constructive induction algorithm in MDR is very simple. However, its implementation for mining patterns from real data can be computationally complex. As with any machine learning algorithm there is always concern about overfitting. That is, machine learning algorithms are good at finding patterns in completely random data. It is often difficult to determine whether a reported pattern is an important signal or just chance. One approach is to estimate the generalizability of a model to independent datasets using methods such as cross-validation. [14] [15] [16] [17] Models that describe random data typically don't generalize. Another approach is to generate many random permutations of the data to see what the data mining algorithm finds when given the chance to overfit. Permutation testing makes it possible to generate an empirical p-value for the result. [18] [19] [20] [21] Replication in independent data may also provide evidence for an MDR model but can be sensitive to difference in the data sets. [22] [23] These approaches have all been shown to be useful for choosing and evaluating MDR models. An important step in a machine learning exercise is interpretation. Several approaches have been used with MDR including entropy analysis [9] [24] and pathway analysis. [25] [26] Tips and approaches for using MDR to model gene-gene interactions have been reviewed. [7] [27]

Extensions to MDR

Numerous extensions to MDR have been introduced. These include family-based methods, [28] [29] [30] fuzzy methods, [31] covariate adjustment, [32] odds ratios, [33] risk scores, [34] survival methods, [35] [36] robust methods, [37] methods for quantitative traits, [38] [39] and many others.

Applications of MDR

MDR has mostly been applied to detecting gene-gene interactions or epistasis in genetic studies of common human diseases such as atrial fibrillation, [40] [41] autism, [42] bladder cancer, [43] [44] [45] breast cancer, [46] cardiovascular disease, [14] hypertension, [47] [48] [49] obesity, [50] [51] pancreatic cancer, [52] prostate cancer [53] [54] [55] and tuberculosis. [56] It has also been applied to other biomedical problems such as the genetic analysis of pharmacology outcomes. [57] [58] [59] A central challenge is the scaling of MDR to big data such as that from genome-wide association studies (GWAS). [60] Several approaches have been used. One approach is to filter the features prior to MDR analysis. [61] This can be done using biological knowledge through tools such as BioFilter. [62] It can also be done using computational tools such as ReliefF. [63] Another approach is to use stochastic search algorithms such as genetic programming to explore the search space of feature combinations. [64] Yet another approach is a brute-force search using high-performance computing. [65] [66] [67]

Implementations

See also

References

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  56. ^ Collins, Ryan L.; Hu, Ting; Wejse, Christian; Sirugo, Giorgio; Williams, Scott M.; Moore, Jason H. (18 February 2013). "Multifactor dimensionality reduction reveals a three-locus epistatic interaction associated with susceptibility to pulmonary tuberculosis". BioData Mining. 6 (1): 4. doi: 10.1186/1756-0381-6-4. PMC  3618340. PMID  23418869.
  57. ^ Wilke, Russell A.; Reif, David M.; Moore, Jason H. (1 November 2005). "Combinatorial Pharmacogenetics". Nature Reviews Drug Discovery. 4 (11): 911–918. doi: 10.1038/nrd1874. ISSN  1474-1776. PMID  16264434. S2CID  11643026.
  58. ^ Motsinger, Alison A.; Ritchie, Marylyn D.; Shafer, Robert W.; Robbins, Gregory K.; Morse, Gene D.; Labbe, Line; Wilkinson, Grant R.; Clifford, David B.; D'Aquila, Richard T. (1 November 2006). "Multilocus genetic interactions and response to efavirenz-containing regimens: an adult AIDS clinical trials group study". Pharmacogenetics and Genomics. 16 (11): 837–845. doi: 10.1097/01.fpc.0000230413.97596.fa. ISSN  1744-6872. PMID  17047492. S2CID  26266170.
  59. ^ Ritchie, Marylyn D.; Motsinger, Alison A. (1 December 2005). "Multifactor dimensionality reduction for detecting gene-gene and gene-environment interactions in pharmacogenomics studies". Pharmacogenomics. 6 (8): 823–834. doi: 10.2217/14622416.6.8.823. ISSN  1462-2416. PMID  16296945. S2CID  10348021.
  60. ^ Moore, Jason H.; Asselbergs, Folkert W.; Williams, Scott M. (15 February 2010). "Bioinformatics challenges for genome-wide association studies". Bioinformatics. 26 (4): 445–455. doi: 10.1093/bioinformatics/btp713. ISSN  1367-4811. PMC  2820680. PMID  20053841.
  61. ^ Sun, Xiangqing; Lu, Qing; Mukherjee, Shubhabrata; Mukheerjee, Shubhabrata; Crane, Paul K.; Elston, Robert; Ritchie, Marylyn D. (1 January 2014). "Analysis pipeline for the epistasis search – statistical versus biological filtering". Frontiers in Genetics. 5: 106. doi: 10.3389/fgene.2014.00106. PMC  4012196. PMID  24817878.
  62. ^ Pendergrass, Sarah A.; Frase, Alex; Wallace, John; Wolfe, Daniel; Katiyar, Neerja; Moore, Carrie; Ritchie, Marylyn D. (30 December 2013). "Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development". BioData Mining. 6 (1): 25. doi: 10.1186/1756-0381-6-25. PMC  3917600. PMID  24378202.
  63. ^ Moore, Jason H. (1 January 2015). "Epistasis Analysis Using ReliefF". Epistasis. Methods in Molecular Biology. Vol. 1253. pp. 315–325. doi: 10.1007/978-1-4939-2155-3_17. ISBN  978-1-4939-2154-6. ISSN  1940-6029. PMID  25403540.
  64. ^ Moore, Jason H.; White, Bill C. (1 January 2007). "Genome-Wide Genetic Analysis Using Genetic Programming: The Critical Need for Expert Knowledge". In Riolo, Rick; Soule, Terence; Worzel, Bill (eds.). Genetic Programming Theory and Practice IV. Genetic and Evolutionary Computation. Springer US. pp. 11–28. doi: 10.1007/978-0-387-49650-4_2. ISBN  9780387333755. S2CID  55188394.
  65. ^ Greene, Casey S.; Sinnott-Armstrong, Nicholas A.; Himmelstein, Daniel S.; Park, Paul J.; Moore, Jason H.; Harris, Brent T. (1 March 2010). "Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS". Bioinformatics. 26 (5): 694–695. doi: 10.1093/bioinformatics/btq009. ISSN  1367-4811. PMC  2828117. PMID  20081222.
  66. ^ Bush, William S.; Dudek, Scott M.; Ritchie, Marylyn D. (1 September 2006). "Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene-gene interactions". Bioinformatics. 22 (17): 2173–2174. doi: 10.1093/bioinformatics/btl347. ISSN  1367-4811. PMC  4939609. PMID  16809395.
  67. ^ Sinnott-Armstrong, Nicholas A.; Greene, Casey S.; Cancare, Fabio; Moore, Jason H. (24 July 2009). "Accelerating epistasis analysis in human genetics with consumer graphics hardware". BMC Research Notes. 2: 149. doi: 10.1186/1756-0500-2-149. ISSN  1756-0500. PMC  2732631. PMID  19630950.
  68. ^ Winham, Stacey J.; Motsinger-Reif, Alison A. (16 August 2011). "An R package implementation of multifactor dimensionality reduction". BioData Mining. 4 (1): 24. doi: 10.1186/1756-0381-4-24. ISSN  1756-0381. PMC  3177775. PMID  21846375.
  69. ^ Calle, M. Luz; Urrea, Víctor; Malats, Núria; Van Steen, Kristel (1 September 2010). "mbmdr: an R package for exploring gene-gene interactions associated with binary or quantitative traits". Bioinformatics. 26 (17): 2198–2199. doi: 10.1093/bioinformatics/btq352. ISSN  1367-4811. PMID  20595460.

Further reading

  • Michalski, R. S., "Pattern Recognition as Knowledge-Guided Computer Induction," Department of Computer Science Reports, No. 927, University of Illinois, Urbana, June 1978.
From Wikipedia, the free encyclopedia

Multifactor dimensionality reduction (MDR) is a statistical approach, also used in machine learning automatic approaches, [1] for detecting and characterizing combinations of attributes or independent variables that interact to influence a dependent or class variable. [2] [3] [4] [5] [6] [7] [8] MDR was designed specifically to identify nonadditive interactions among discrete variables that influence a binary outcome and is considered a nonparametric and model-free alternative to traditional statistical methods such as logistic regression.

The basis of the MDR method is a constructive induction or feature engineering algorithm that converts two or more variables or attributes to a single attribute. [9] This process of constructing a new attribute changes the representation space of the data. [10] The end goal is to create or discover a representation that facilitates the detection of nonlinear or nonadditive interactions among the attributes such that prediction of the class variable is improved over that of the original representation of the data.

Illustrative example

Consider the following simple example using the exclusive OR (XOR) function. XOR is a logical operator that is commonly used in data mining and machine learning as an example of a function that is not linearly separable. The table below represents a simple dataset where the relationship between the attributes (X1 and X2) and the class variable (Y) is defined by the XOR function such that Y = X1 XOR X2.

Table 1

X1 X2 Y
0 0 0
0 1 1
1 0 1
1 1 0

A machine learning algorithm would need to discover or approximate the XOR function in order to accurately predict Y using information about X1 and X2. An alternative strategy would be to first change the representation of the data using constructive induction to facilitate predictive modeling. The MDR algorithm would change the representation of the data (X1 and X2) in the following manner. MDR starts by selecting two attributes. In this simple example, X1 and X2 are selected. Each combination of values for X1 and X2 are examined and the number of times Y=1 and/or Y=0 is counted. In this simple example, Y=1 occurs zero times and Y=0 occurs once for the combination of X1=0 and X2=0. With MDR, the ratio of these counts is computed and compared to a fixed threshold. Here, the ratio of counts is 0/1 which is less than our fixed threshold of 1. Since 0/1 < 1 we encode a new attribute (Z) as a 0. When the ratio is greater than one we encode Z as a 1. This process is repeated for all unique combinations of values for X1 and X2. Table 2 illustrates our new transformation of the data.

Table 2

Z Y
0 0
1 1
1 1
0 0

The machine learning algorithm now has much less work to do to find a good predictive function. In fact, in this very simple example, the function Y = Z has a classification accuracy of 1. A nice feature of constructive induction methods such as MDR is the ability to use any data mining or machine learning method to analyze the new representation of the data. Decision trees, neural networks, or a naive Bayes classifier could be used in combination with measures of model quality such as balanced accuracy [11] [12] and mutual information. [13]

Machine learning with MDR

As illustrated above, the basic constructive induction algorithm in MDR is very simple. However, its implementation for mining patterns from real data can be computationally complex. As with any machine learning algorithm there is always concern about overfitting. That is, machine learning algorithms are good at finding patterns in completely random data. It is often difficult to determine whether a reported pattern is an important signal or just chance. One approach is to estimate the generalizability of a model to independent datasets using methods such as cross-validation. [14] [15] [16] [17] Models that describe random data typically don't generalize. Another approach is to generate many random permutations of the data to see what the data mining algorithm finds when given the chance to overfit. Permutation testing makes it possible to generate an empirical p-value for the result. [18] [19] [20] [21] Replication in independent data may also provide evidence for an MDR model but can be sensitive to difference in the data sets. [22] [23] These approaches have all been shown to be useful for choosing and evaluating MDR models. An important step in a machine learning exercise is interpretation. Several approaches have been used with MDR including entropy analysis [9] [24] and pathway analysis. [25] [26] Tips and approaches for using MDR to model gene-gene interactions have been reviewed. [7] [27]

Extensions to MDR

Numerous extensions to MDR have been introduced. These include family-based methods, [28] [29] [30] fuzzy methods, [31] covariate adjustment, [32] odds ratios, [33] risk scores, [34] survival methods, [35] [36] robust methods, [37] methods for quantitative traits, [38] [39] and many others.

Applications of MDR

MDR has mostly been applied to detecting gene-gene interactions or epistasis in genetic studies of common human diseases such as atrial fibrillation, [40] [41] autism, [42] bladder cancer, [43] [44] [45] breast cancer, [46] cardiovascular disease, [14] hypertension, [47] [48] [49] obesity, [50] [51] pancreatic cancer, [52] prostate cancer [53] [54] [55] and tuberculosis. [56] It has also been applied to other biomedical problems such as the genetic analysis of pharmacology outcomes. [57] [58] [59] A central challenge is the scaling of MDR to big data such as that from genome-wide association studies (GWAS). [60] Several approaches have been used. One approach is to filter the features prior to MDR analysis. [61] This can be done using biological knowledge through tools such as BioFilter. [62] It can also be done using computational tools such as ReliefF. [63] Another approach is to use stochastic search algorithms such as genetic programming to explore the search space of feature combinations. [64] Yet another approach is a brute-force search using high-performance computing. [65] [66] [67]

Implementations

See also

References

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  43. ^ Andrew, Angeline S.; Nelson, Heather H.; Kelsey, Karl T.; Moore, Jason H.; Meng, Alexis C.; Casella, Daniel P.; Tosteson, Tor D.; Schned, Alan R.; Karagas, Margaret R. (1 May 2006). "Concordance of multiple analytical approaches demonstrates a complex relationship between DNA repair gene SNPs, smoking and bladder cancer susceptibility". Carcinogenesis. 27 (5): 1030–1037. doi: 10.1093/carcin/bgi284. ISSN  0143-3334. PMID  16311243.
  44. ^ Andrew, Angeline S.; Karagas, Margaret R.; Nelson, Heather H.; Guarrera, Simonetta; Polidoro, Silvia; Gamberini, Sara; Sacerdote, Carlotta; Moore, Jason H.; Kelsey, Karl T. (1 January 2008). "DNA Repair Polymorphisms Modify Bladder Cancer Risk: A Multi-factor Analytic Strategy". Human Heredity. 65 (2): 105–118. doi: 10.1159/000108942. ISSN  0001-5652. PMC  2857629. PMID  17898541.
  45. ^ Andrew, Angeline S.; Hu, Ting; Gu, Jian; Gui, Jiang; Ye, Yuanqing; Marsit, Carmen J.; Kelsey, Karl T.; Schned, Alan R.; Tanyos, Sam A. (1 January 2012). "HSD3B and gene-gene interactions in a pathway-based analysis of genetic susceptibility to bladder cancer". PLOS ONE. 7 (12): e51301. Bibcode: 2012PLoSO...751301A. doi: 10.1371/journal.pone.0051301. ISSN  1932-6203. PMC  3526593. PMID  23284679.
  46. ^ Cao, Jingjing; Luo, Chenglin; Yan, Rui; Peng, Rui; Wang, Kaijuan; Wang, Peng; Ye, Hua; Song, Chunhua (1 December 2016). "rs15869 at miRNA binding site in BRCA2 is associated with breast cancer susceptibility". Medical Oncology. 33 (12): 135. doi: 10.1007/s12032-016-0849-2. ISSN  1357-0560. PMID  27807724. S2CID  26042128.
  47. ^ Williams, Scott M.; Ritchie, Marylyn D.; III, John A. Phillips; Dawson, Elliot; Prince, Melissa; Dzhura, Elvira; Willis, Alecia; Semenya, Amma; Summar, Marshall (1 January 2004). "Multilocus Analysis of Hypertension: A Hierarchical Approach". Human Heredity. 57 (1): 28–38. doi: 10.1159/000077387. ISSN  0001-5652. PMID  15133310. S2CID  21079485.
  48. ^ Sanada, Hironobu; Yatabe, Junichi; Midorikawa, Sanae; Hashimoto, Shigeatsu; Watanabe, Tsuyoshi; Moore, Jason H.; Ritchie, Marylyn D.; Williams, Scott M.; Pezzullo, John C. (1 March 2006). "Single-Nucleotide Polymorphisms for Diagnosis of Salt-Sensitive Hypertension". Clinical Chemistry. 52 (3): 352–360. doi: 10.1373/clinchem.2005.059139. ISSN  0009-9147. PMID  16439609.
  49. ^ Moore, Jason H.; Williams, Scott M. (1 January 2002). "New strategies for identifying gene-gene interactions in hypertension". Annals of Medicine. 34 (2): 88–95. doi: 10.1080/07853890252953473. ISSN  0785-3890. PMID  12108579. S2CID  25398042.
  50. ^ De, Rishika; Verma, Shefali S.; Holzinger, Emily; Hall, Molly; Burt, Amber; Carrell, David S.; Crosslin, David R.; Jarvik, Gail P.; Kuivaniemi, Helena (1 February 2017). "Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts" (PDF). Human Genetics. 136 (2): 165–178. doi: 10.1007/s00439-016-1738-7. ISSN  1432-1203. PMID  27848076. S2CID  24702049.
  51. ^ De, Rishika; Verma, Shefali S.; Drenos, Fotios; Holzinger, Emily R.; Holmes, Michael V.; Hall, Molly A.; Crosslin, David R.; Carrell, David S.; Hakonarson, Hakon (1 January 2015). "Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)". BioData Mining. 8: 41. doi: 10.1186/s13040-015-0074-0. PMC  4678717. PMID  26674805.
  52. ^ Duell, Eric J.; Bracci, Paige M.; Moore, Jason H.; Burk, Robert D.; Kelsey, Karl T.; Holly, Elizabeth A. (1 June 2008). "Detecting pathway-based gene-gene and gene-environment interactions in pancreatic cancer". Cancer Epidemiology, Biomarkers & Prevention. 17 (6): 1470–1479. doi: 10.1158/1055-9965.EPI-07-2797. ISSN  1055-9965. PMC  4410856. PMID  18559563.
  53. ^ Xu, Jianfeng; Lowey, James; Wiklund, Fredrik; Sun, Jielin; Lindmark, Fredrik; Hsu, Fang-Chi; Dimitrov, Latchezar; Chang, Baoli; Turner, Aubrey R. (1 November 2005). "The Interaction of Four Genes in the Inflammation Pathway Significantly Predicts Prostate Cancer Risk". Cancer Epidemiology, Biomarkers & Prevention. 14 (11): 2563–2568. doi: 10.1158/1055-9965.EPI-05-0356. ISSN  1055-9965. PMID  16284379.
  54. ^ Lavender, Nicole A.; Rogers, Erica N.; Yeyeodu, Susan; Rudd, James; Hu, Ting; Zhang, Jie; Brock, Guy N.; Kimbro, Kevin S.; Moore, Jason H. (30 April 2012). "Interaction among apoptosis-associated sequence variants and joint effects on aggressive prostate cancer". BMC Medical Genomics. 5: 11. doi: 10.1186/1755-8794-5-11. ISSN  1755-8794. PMC  3355002. PMID  22546513.
  55. ^ Lavender, Nicole A.; Benford, Marnita L.; VanCleave, Tiva T.; Brock, Guy N.; Kittles, Rick A.; Moore, Jason H.; Hein, David W.; Kidd, La Creis R. (16 November 2009). "Examination of polymorphic glutathione S-transferase (GST) genes, tobacco smoking and prostate cancer risk among men of African descent: a case-control study". BMC Cancer. 9: 397. doi: 10.1186/1471-2407-9-397. ISSN  1471-2407. PMC  2783040. PMID  19917083.
  56. ^ Collins, Ryan L.; Hu, Ting; Wejse, Christian; Sirugo, Giorgio; Williams, Scott M.; Moore, Jason H. (18 February 2013). "Multifactor dimensionality reduction reveals a three-locus epistatic interaction associated with susceptibility to pulmonary tuberculosis". BioData Mining. 6 (1): 4. doi: 10.1186/1756-0381-6-4. PMC  3618340. PMID  23418869.
  57. ^ Wilke, Russell A.; Reif, David M.; Moore, Jason H. (1 November 2005). "Combinatorial Pharmacogenetics". Nature Reviews Drug Discovery. 4 (11): 911–918. doi: 10.1038/nrd1874. ISSN  1474-1776. PMID  16264434. S2CID  11643026.
  58. ^ Motsinger, Alison A.; Ritchie, Marylyn D.; Shafer, Robert W.; Robbins, Gregory K.; Morse, Gene D.; Labbe, Line; Wilkinson, Grant R.; Clifford, David B.; D'Aquila, Richard T. (1 November 2006). "Multilocus genetic interactions and response to efavirenz-containing regimens: an adult AIDS clinical trials group study". Pharmacogenetics and Genomics. 16 (11): 837–845. doi: 10.1097/01.fpc.0000230413.97596.fa. ISSN  1744-6872. PMID  17047492. S2CID  26266170.
  59. ^ Ritchie, Marylyn D.; Motsinger, Alison A. (1 December 2005). "Multifactor dimensionality reduction for detecting gene-gene and gene-environment interactions in pharmacogenomics studies". Pharmacogenomics. 6 (8): 823–834. doi: 10.2217/14622416.6.8.823. ISSN  1462-2416. PMID  16296945. S2CID  10348021.
  60. ^ Moore, Jason H.; Asselbergs, Folkert W.; Williams, Scott M. (15 February 2010). "Bioinformatics challenges for genome-wide association studies". Bioinformatics. 26 (4): 445–455. doi: 10.1093/bioinformatics/btp713. ISSN  1367-4811. PMC  2820680. PMID  20053841.
  61. ^ Sun, Xiangqing; Lu, Qing; Mukherjee, Shubhabrata; Mukheerjee, Shubhabrata; Crane, Paul K.; Elston, Robert; Ritchie, Marylyn D. (1 January 2014). "Analysis pipeline for the epistasis search – statistical versus biological filtering". Frontiers in Genetics. 5: 106. doi: 10.3389/fgene.2014.00106. PMC  4012196. PMID  24817878.
  62. ^ Pendergrass, Sarah A.; Frase, Alex; Wallace, John; Wolfe, Daniel; Katiyar, Neerja; Moore, Carrie; Ritchie, Marylyn D. (30 December 2013). "Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development". BioData Mining. 6 (1): 25. doi: 10.1186/1756-0381-6-25. PMC  3917600. PMID  24378202.
  63. ^ Moore, Jason H. (1 January 2015). "Epistasis Analysis Using ReliefF". Epistasis. Methods in Molecular Biology. Vol. 1253. pp. 315–325. doi: 10.1007/978-1-4939-2155-3_17. ISBN  978-1-4939-2154-6. ISSN  1940-6029. PMID  25403540.
  64. ^ Moore, Jason H.; White, Bill C. (1 January 2007). "Genome-Wide Genetic Analysis Using Genetic Programming: The Critical Need for Expert Knowledge". In Riolo, Rick; Soule, Terence; Worzel, Bill (eds.). Genetic Programming Theory and Practice IV. Genetic and Evolutionary Computation. Springer US. pp. 11–28. doi: 10.1007/978-0-387-49650-4_2. ISBN  9780387333755. S2CID  55188394.
  65. ^ Greene, Casey S.; Sinnott-Armstrong, Nicholas A.; Himmelstein, Daniel S.; Park, Paul J.; Moore, Jason H.; Harris, Brent T. (1 March 2010). "Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS". Bioinformatics. 26 (5): 694–695. doi: 10.1093/bioinformatics/btq009. ISSN  1367-4811. PMC  2828117. PMID  20081222.
  66. ^ Bush, William S.; Dudek, Scott M.; Ritchie, Marylyn D. (1 September 2006). "Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene-gene interactions". Bioinformatics. 22 (17): 2173–2174. doi: 10.1093/bioinformatics/btl347. ISSN  1367-4811. PMC  4939609. PMID  16809395.
  67. ^ Sinnott-Armstrong, Nicholas A.; Greene, Casey S.; Cancare, Fabio; Moore, Jason H. (24 July 2009). "Accelerating epistasis analysis in human genetics with consumer graphics hardware". BMC Research Notes. 2: 149. doi: 10.1186/1756-0500-2-149. ISSN  1756-0500. PMC  2732631. PMID  19630950.
  68. ^ Winham, Stacey J.; Motsinger-Reif, Alison A. (16 August 2011). "An R package implementation of multifactor dimensionality reduction". BioData Mining. 4 (1): 24. doi: 10.1186/1756-0381-4-24. ISSN  1756-0381. PMC  3177775. PMID  21846375.
  69. ^ Calle, M. Luz; Urrea, Víctor; Malats, Núria; Van Steen, Kristel (1 September 2010). "mbmdr: an R package for exploring gene-gene interactions associated with binary or quantitative traits". Bioinformatics. 26 (17): 2198–2199. doi: 10.1093/bioinformatics/btq352. ISSN  1367-4811. PMID  20595460.

Further reading

  • Michalski, R. S., "Pattern Recognition as Knowledge-Guided Computer Induction," Department of Computer Science Reports, No. 927, University of Illinois, Urbana, June 1978.

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