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- Publisher Website: 10.1186/1471-2156-14-82
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Article: An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data.(Methodology article)(Report)
Title | An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data.(Methodology article)(Report) |
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Authors | |
Keywords | Expectation-maximization Algorithm -- Usage Genetic Research -- Methods Haplotypes -- Research |
Issue Date | 2013 |
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcgenet/ |
Citation | BMC Genetics, 2013, v. 14, p. 82-82 How to Cite? |
Abstract | Background Pooling is a cost effective way to collect data for genetic association studies, particularly for rare genetic variants. It is of interest to estimate the haplotype frequencies, which contain more information than single locus statistics. By viewing the pooled genotype data as incomplete data, the expectation-maximization (EM) algorithm is the natural algorithm to use, but it is computationally intensive. A recent proposal to reduce the computational burden is to make use of database information to form a list of frequently occurring haplotypes, and to restrict the haplotypes to come from this list only in implementing the EM algorithm. There is, however, the danger of using an incorrect list, and there may not be enough database information to form a list externally in some applications. Results We investigate the possibility of creating an internal list from the data at hand. One way to form such a list is to collapse the observed total minor allele frequencies to ?zero? or ?at least one?, which is shown to have the desirable effect of amplifying the haplotype frequencies. To improve coverage, we propose ways to add and remove haplotypes from the list, and a benchmarking method to determine the frequency threshold for removing haplotypes. Simulation results show that the EM estimates based on a suitably augmented and trimmed collapsed data list (ATCDL) perform satisfactorily. In two scenarios involving 25 and 32 loci respectively, the EM-ATCDL estimates outperform the EM estimates based on other lists as well as the collapsed data maximum likelihood estimates. Conclusions The proposed augmented and trimmed CD list is a useful list for the EM algorithm to base upon in estimating the haplotype distributions of rare variants. It can handle more markers and larger pool size than existing methods, and the resulting EM-ATCDL estimates are more efficient than the EM estimates based on other lists. |
Persistent Identifier | http://hdl.handle.net/10722/221673 |
ISSN | 2022 Impact Factor: 2.9 2020 SCImago Journal Rankings: 0.856 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Kuk, AYC | - |
dc.contributor.author | Li, X | - |
dc.contributor.author | Xu, J | - |
dc.date.accessioned | 2015-12-04T15:29:00Z | - |
dc.date.available | 2015-12-04T15:29:00Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | BMC Genetics, 2013, v. 14, p. 82-82 | - |
dc.identifier.issn | 1471-2156 | - |
dc.identifier.uri | http://hdl.handle.net/10722/221673 | - |
dc.description.abstract | Background Pooling is a cost effective way to collect data for genetic association studies, particularly for rare genetic variants. It is of interest to estimate the haplotype frequencies, which contain more information than single locus statistics. By viewing the pooled genotype data as incomplete data, the expectation-maximization (EM) algorithm is the natural algorithm to use, but it is computationally intensive. A recent proposal to reduce the computational burden is to make use of database information to form a list of frequently occurring haplotypes, and to restrict the haplotypes to come from this list only in implementing the EM algorithm. There is, however, the danger of using an incorrect list, and there may not be enough database information to form a list externally in some applications. Results We investigate the possibility of creating an internal list from the data at hand. One way to form such a list is to collapse the observed total minor allele frequencies to ?zero? or ?at least one?, which is shown to have the desirable effect of amplifying the haplotype frequencies. To improve coverage, we propose ways to add and remove haplotypes from the list, and a benchmarking method to determine the frequency threshold for removing haplotypes. Simulation results show that the EM estimates based on a suitably augmented and trimmed collapsed data list (ATCDL) perform satisfactorily. In two scenarios involving 25 and 32 loci respectively, the EM-ATCDL estimates outperform the EM estimates based on other lists as well as the collapsed data maximum likelihood estimates. Conclusions The proposed augmented and trimmed CD list is a useful list for the EM algorithm to base upon in estimating the haplotype distributions of rare variants. It can handle more markers and larger pool size than existing methods, and the resulting EM-ATCDL estimates are more efficient than the EM estimates based on other lists. | - |
dc.language | eng | - |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcgenet/ | - |
dc.relation.ispartof | BMC Genetics | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Expectation-maximization Algorithm -- Usage | - |
dc.subject | Genetic Research -- Methods | - |
dc.subject | Haplotypes -- Research | - |
dc.title | An EM algorithm based on an internal list for estimating haplotype distributions of rare variants from pooled genotype data.(Methodology article)(Report) | - |
dc.type | Article | - |
dc.identifier.email | Xu, J: xujf@hku.hk | - |
dc.identifier.authority | Xu, J=rp02086 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/1471-2156-14-82 | - |
dc.identifier.pmid | 24034507 | - |
dc.identifier.pmcid | PMC3847674 | - |
dc.identifier.scopus | eid_2-s2.0-84884357445 | - |
dc.identifier.volume | 14 | - |
dc.identifier.spage | 82 | - |
dc.identifier.epage | 82 | - |
dc.identifier.isi | WOS:000324519500001 | - |
dc.identifier.issnl | 1471-2156 | - |