Evidence map›Paper›PMID 24618466›Full record

ArticleBioinformatics (Oxford, England)2014

FISH: fast and accurate diploid genotype imputation via segmental hidden Markov model.

Lei Zhang, Yu-Fang Pei, Xiaoying Fu, Yong Lin, Yu-Ping Wang, Hong-Wen Deng

Erratum issuedAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 9 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 9 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Four pleiotropic loci associated with fat mass and lean mass.International journal of obesity (2005) · 2020
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  8. Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
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  12. Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2020
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  15. Genome-wide identification of mOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2018
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  16. Genome-Wide Identification of NFrontiers in genetics · 2018
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors.

Lei ZhangSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, ChinaSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.
Yu-Fang PeiSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, ChinaSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.
Xiaoying FuSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.
Yong LinSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.
Yu-Ping WangSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.
Hong-Wen DengSchool of Public Health, Xi'an Jiaotong University, Shaanxi, China, Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, USA and Center of System Biomedical Sciences, University of Shanghai for Science and Technology, Shanghai, China.

Funding

Proteome-wide Expression Study of Osteogenic CellsP50AR055081 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2007 to 2012
$5.0M
ROBUST AND POWERFUL TEST OF CANDIDATE GENES TO BONE MASSR01AR050496 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2004 to 2013
$3.8M
Epigenomewide DNA Methylation Study for Osteoporosis RiskR01AR059781 · NIAMS · TULANE UNIVERSITY OF LOUISIANA · PI DENG, HONG-WEN · 2012 to 2016
$3.1M
Identification of Proteins Important for Male OsteoporosisR01AR057049 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2009 to 2013
$2.4M
Genomic search for bone mass QTLsR01AG026564 · NIA · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2007 to 2010
$2.3M
Genome-wide association study of periodontitisRC2DE020756 · NIDCR · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN, GENCO, ROBERT J · 2009 to 2009
$173k
Genetics of Osteoporotic Fractures in ChineseR03TW008221 · FIC · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2009 to 2011
$171k
FIC NIH HHS R03 TW008221FIC NIH HHS R03TW008221NIAMS NIH HHS P50 AR055081NIAMS NIH HHS P50AR055081NIAMS NIH HHS R01 AR050496NIAMS NIH HHS R01AR050496NIAMS NIH HHS R01 AR057049NIAMS NIH HHS R01AR057049NIAMS NIH HHS R01 AR059781NIA NIH HHS R01 AG026564NIA NIH HHS R01AG026564NIDCR NIH HHS RC2 DE020756NIDCR NIH HHS RC2DE020756
6 · The paper itself

Abstract

motivationFast and accurate genotype imputation is necessary for facilitating gene-mapping studies, especially with the ever increasing numbers of both common and rare variants generated by high-throughput-sequencing experiments. However, most of the existing imputation approaches suffer from either inaccurate results or heavy computational demand.

resultsIn this article, aiming to perform fast and accurate genotype-imputation analysis, we propose a novel, fast and yet accurate method to impute diploid genotypes. Specifically, we extend a hidden Markov model that is widely used to describe haplotype structures. But we model hidden states onto single reference haplotypes rather than onto pairs of haplotypes. Consequently the computational complexity is linear to size of reference haplotypes. We further develop an algorithm 'merge-and-recover (MAR)' to speed up the calculation. Working on compact representation of segmental reference haplotypes, the MAR algorithm always calculates an exact form of transition probabilities regardless of partition of segments. Both simulation studies and real-data analyses demonstrated that our proposed method was comparable to most of the existing popular methods in terms of imputation accuracy, but was much more efficient in terms of computation. The MAR algorithm can further speed up the calculation by several folds without loss of accuracy. The proposed method will be useful in large-scale imputation studies with a large number of reference subjects. AVAILABILITY: The implemented multi-threading software FISH is freely available for academic use at https://sites.google.com/site/lzhanghomepage/FISH.

Indexed as

DiploidyAlgorithmsGenotypeHaplotypesHigh-Throughput Nucleotide SequencingMarkov ChainsSoftware

Identifiers

PMID24618466
PMCPMC4071209

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