Relating HIV-1 Sequence Variation to Replication Capacity via Trees and Forests
Gespeichert in:
Verfasser / Beitragende:
[Mark R Segal, Jason D Barbour, Robert M Grant]
Ort, Verlag, Jahr:
2004
Enthalten in:
Statistical Applications in Genetics and Molecular Biology, 3/1(2004-02-12), 1-18
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.2202/1544-6115.1031 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.2202/1544-6115.1031 | ||
| 245 | 0 | 0 | |a Relating HIV-1 Sequence Variation to Replication Capacity via Trees and Forests |h [Elektronische Daten] |c [Mark R Segal, Jason D Barbour, Robert M Grant] |
| 520 | 3 | |a The problem of relating genotype (as represented by amino acid sequence) to phenotypes is distinguished from standard regression problems by the nature of sequence data. Here we investigate an instance of such a problem where the phenotype of interest is HIV-1 replication capacity and contiguous segments of protease and reverse transcriptase sequence constitutes genotype. A variety of data analytic methods have been proposed in this context. Shortcomings of select techniques are contrasted with the advantages afforded by tree-structured methods. However, tree-structured methods, in turn, have been criticized on grounds of only enjoying modest predictive performance. A number of ensemble approaches (bagging, boosting, random forests) have recently emerged, devised to overcome this deficiency. We evaluate random forests as applied in this setting, and detail why prediction gains obtained in other situations are not realized. Other approaches including logic regression, support vector machines and neural networks are also applied. We interpret results in terms of HIV-1 reverse transcriptase structure and function. | |
| 540 | |a ©2011 Walter de Gruyter GmbH & Co. KG, Berlin/Boston | ||
| 690 | 7 | |a Multivariate Analysis |2 nationallicence | |
| 690 | 7 | |a Protease |2 nationallicence | |
| 690 | 7 | |a Random Forests |2 nationallicence | |
| 690 | 7 | |a Reverse Transcriptase |2 nationallicence | |
| 690 | 7 | |a Tree-Structured Methods |2 nationallicence | |
| 700 | 1 | |a Segal |D Mark R. |u University of California, San Francisco |4 aut | |
| 700 | 1 | |a Barbour |D Jason D. |u University of California, San Francisco |4 aut | |
| 700 | 1 | |a Grant |D Robert M. |u University of California, San Francisco |4 aut | |
| 773 | 0 | |t Statistical Applications in Genetics and Molecular Biology |d De Gruyter |g 3/1(2004-02-12), 1-18 |q 3:1<1 |1 2004 |2 3 |o sagmb | |
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| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.2202/1544-6115.1031 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Segal |D Mark R. |u University of California, San Francisco |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Barbour |D Jason D. |u University of California, San Francisco |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Grant |D Robert M. |u University of California, San Francisco |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Statistical Applications in Genetics and Molecular Biology |d De Gruyter |g 3/1(2004-02-12), 1-18 |q 3:1<1 |1 2004 |2 3 |o sagmb | ||
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| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||