Resampling-based tests for Lasso in genome-wide association studies.

Abstract:

BACKGROUND:Genome-wide association studies involve detecting association between millions of genetic variants and a trait, which typically use univariate regression to test association between each single variant and the phenotype. Alternatively, Lasso penalized regression allows one to jointly model the relationship between all genetic variants and the phenotype. However, it is unclear how to best conduct inference on the individual Lasso coefficients, especially in high-dimensional settings. METHODS:We consider six methods for testing the Lasso coefficients: two permutation (Lasso-Ayers, Lasso-PL) and one analytic approach (Lasso-AL) to select the penalty parameter for type-1-error control, residual bootstrap (Lasso-RB), modified residual bootstrap (Lasso-MRB), and a permutation test (Lasso-PT). Methods are compared via simulations and application to the Minnesota Center for Twins and Family Study. RESULTS:We show that for finite sample sizes with increasing number of null predictors, Lasso-RB, Lasso-MRB, and Lasso-PT fail to be viable methods of inference. However, Lasso-PL and Lasso-AL remain fast and powerful tools for conducting inference with the Lasso, even in high-dimensions. CONCLUSION:Our results suggest that the proposed permutation selection procedure (Lasso-PL) and the analytic selection method (Lasso-AL) are fast and powerful alternatives to the standard univariate analysis in genome-wide association studies.

journal_name

BMC Genet

journal_title

BMC genetics

authors

Arbet J,McGue M,Chatterjee S,Basu S

doi

10.1186/s12863-017-0533-3

subject

Has Abstract

pub_date

2017-07-24 00:00:00

pages

70

issue

1

issn

1471-2156

pii

10.1186/s12863-017-0533-3

journal_volume

18

pub_type

杂志文章
  • Correction to: Landraces of snake melon, an ancient Middle Eastern crop, reveal extensive morphological and DNA diversity for potential genetic improvement.

    abstract::Following publication of the original article [1], the authors reported the need for a more detailed acknowledgement of the source of the samples that were analyzed and their coordinates, which are discussed in the 'Methods' section of the article. This Correction provides an addition to the 'Methods' section, and a s...

    journal_title:BMC genetics

    pub_type: 杂志文章,已发布勘误

    doi:10.1186/s12863-018-0632-9

    authors: Omari S,Kamenir Y,Benichou JIC,Pariente S,Sela H,Perl-Treves R

    更新日期:2018-07-12 00:00:00

  • Genome-enabled predictions for binomial traits in sugar beet populations.

    abstract:BACKGROUND:Genomic information can be used to predict not only continuous but also categorical (e.g. binomial) traits. Several traits of interest in human medicine and agriculture present a discrete distribution of phenotypes (e.g. disease status). Root vigor in sugar beet (B. vulgaris) is an example of binomial trait ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-15-87

    authors: Biscarini F,Stevanato P,Broccanello C,Stella A,Saccomani M

    更新日期:2014-07-22 00:00:00

  • Towards systems genetic analyses in barley: Integration of phenotypic, expression and genotype data into GeneNetwork.

    abstract:BACKGROUND:A typical genetical genomics experiment results in four separate data sets; genotype, gene expression, higher-order phenotypic data and metadata that describe the protocols, processing and the array platform. Used in concert, these data sets provide the opportunity to perform genetic analysis at a systems le...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-9-73

    authors: Druka A,Druka I,Centeno AG,Li H,Sun Z,Thomas WT,Bonar N,Steffenson BJ,Ullrich SE,Kleinhofs A,Wise RP,Close TJ,Potokina E,Luo Z,Wagner C,Schweizer GF,Marshall DF,Kearsey MJ,Williams RW,Waugh R

    更新日期:2008-11-18 00:00:00

  • Cytoplasm affects grain weight and filled-grain ratio in indica rice.

    abstract:BACKGROUND:Cytoplasmic effects on agronomic traits--involving cytoplasmic and nuclear genomes of either different species or different cultivars--are well documented in wheat but have seldom been demonstrated in rice (Oryza sativa L.). To detect cytoplasmic effects, we introgressed the nuclear genomes of three indica c...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-12-53

    authors: Tao D,Xu P,Zhou J,Deng X,Li J,Deng W,Yang J,Yang G,Li Q,Hu F

    更新日期:2011-06-01 00:00:00

  • P53 codon 72 polymorphism, human papillomavirus infection, and their interaction to oral carcinoma susceptibility.

    abstract:BACKGROUND:Tumor suppressor gene p53 plays an important role in the maintenance of the genomic integrity, and mutation in the gene may alter an individual's susceptibility to various carcinomas. P53 Arg72Pro or codon 72 polymorphism has been indicated to increase the risk of developing certain cancers such as bladder c...

    journal_title:BMC genetics

    pub_type: 杂志文章,meta分析

    doi:10.1186/s12863-015-0235-7

    authors: Hou J,Gu Y,Hou W,Wu S,Lou Y,Yang W,Zhu L,Hu Y,Sun M,Xue H

    更新日期:2015-06-30 00:00:00

  • A multi-marker test based on family data in genome-wide association study.

    abstract:BACKGROUND:Complex diseases are believed to be the results of many genes and environmental factors. Hence, multi-marker methods that can use the information of markers from different genes are appropriate for mapping complex disease genes. There already have been several multi-marker methods proposed for case-control s...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-8-65

    authors: Zhang Z,Zhang S,Sha Q

    更新日期:2007-09-25 00:00:00

  • Whole genome scan reveals the genetic signature of African Ankole cattle breed and potential for higher quality beef.

    abstract:BACKGROUND:Africa is home to numerous cattle breeds whose diversity has been shaped by subtle combinations of human and natural selection. African Sanga cattle are an intermediate type of cattle resulting from interbreeding between Bos taurus and Bos indicus subspecies. Recently, research has asserted the potential of ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-016-0467-1

    authors: Taye M,Kim J,Yoon SH,Lee W,Hanotte O,Dessie T,Kemp S,Mwai OA,Caetano-Anolles K,Cho S,Oh SJ,Lee HK,Kim H

    更新日期:2017-02-09 00:00:00

  • Multiple telophase arrest bypassed (tab) mutants alleviate the essential requirement for Cdc15 in exit from mitosis in S. cerevisiae.

    abstract:BACKGROUND:The Mitotic Exit Network (MEN) proteins - including the protein kinase Cdc15 and the protein phosphatase Cdc14 - are essential for exit from mitosis in Saccharomyces cerevisiae. To identify downstream targets of the MEN, we sought telophase arrest bypassed (tab) mutations that bypassed the essential requirem...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-3-4

    authors: Shou W,Deshaies RJ

    更新日期:2002-03-12 00:00:00

  • Bivariate linkage analysis of cholesterol and triglyceride levels in the Framingham Heart Study.

    abstract::We performed a bivariate analysis on cholesterol and triglyceride levels on data from the Framingham Heart Study using a new score statistic developed for the detection of potential pleiotropic, or cluster, genes. Univariate score statistics were also computed for each trait. At a significance level 0.001, linkage sig...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-4-S1-S62

    authors: Zhang X,Wang K,Framingham Heart Study.

    更新日期:2003-12-31 00:00:00

  • The effect of rare alleles on estimated genomic relationships from whole genome sequence data.

    abstract:BACKGROUND:Relationships between individuals and inbreeding coefficients are commonly used for breeding decisions, but may be affected by the type of data used for their estimation. The proportion of variants with low Minor Allele Frequency (MAF) is larger in whole genome sequence (WGS) data compared to Single Nucleoti...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-015-0185-0

    authors: Eynard SE,Windig JJ,Leroy G,van Binsbergen R,Calus MP

    更新日期:2015-03-12 00:00:00

  • Impact of the diagnosis definition on linkage detection.

    abstract::Previous genome scan linkage analyses of the disease Kofendrerd Personality Disorder (KPD) with microsatellites led to detect some regions on chromosomes 1, 3, 5, and 9 that were identical for the three populations AI, KA, and DA but with large differences in significance levels. These differences in results may be ex...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-S1-S140

    authors: Dizier MH,Génin E,Babron MC,Bourgain C

    更新日期:2005-12-30 00:00:00

  • Genome-wide analysis of long non-coding RNAs in Catalpa bungei and their potential function in floral transition using high-throughput sequencing.

    abstract:BACKGROUND:Long non-coding RNAs (lncRNAs) have crucial roles in various biological regulatory processes. However, the study of lncRNAs is limited in woody plants. Catalpa bungei is a valuable ornamental tree with a long cultivation history in China, and a deeper understanding of the floral transition mechanism in C. bu...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-018-0671-2

    authors: Wang Z,Zhu T,Ma W,Wang N,Qu G,Zhang S,Wang J

    更新日期:2018-09-20 00:00:00

  • Consomic mouse strain selection based on effect size measurement, statistical significance testing and integrated behavioral z-scoring: focus on anxiety-related behavior and locomotion.

    abstract:BACKGROUND:Selecting chromosome substitution strains (CSSs, also called consomic strains/lines) used in the search for quantitative trait loci (QTLs) consistently requires the identification of the respective phenotypic trait of interest and is simply based on a significant difference between a consomic and host strain...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-016-0411-4

    authors: Labots M,Laarakker MC,Ohl F,van Lith HA

    更新日期:2016-06-29 00:00:00

  • Interval estimation of disease loci: development and applications of new linkage methods.

    abstract::Three variants of the confidence set inference (CSI) procedure were proposed and applied to both the simulated and the Collaborative Study on the Genetics of Alcoholism (COGA) data. For each of the two applications, we first performed a preliminary genome scan study based on the microsatellite markers using the GENEHU...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-S1-S21

    authors: Papachristou C,Lin S

    更新日期:2005-12-30 00:00:00

  • Conserved genomic organisation of Group B Sox genes in insects.

    abstract:BACKGROUND:Sox domain containing genes are important metazoan transcriptional regulators implicated in a wide rage of developmental processes. The vertebrate B subgroup contains the Sox1, Sox2 and Sox3 genes that have early functions in neural development. Previous studies show that Drosophila Group B genes have been f...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-26

    authors: McKimmie C,Woerfel G,Russell S

    更新日期:2005-05-19 00:00:00

  • Characterization of the late embryogenesis abundant (LEA) proteins family and their role in drought stress tolerance in upland cotton.

    abstract:BACKGROUND:Late embryogenesis abundant (LEA) proteins are large groups of hydrophilic proteins with major role in drought and other abiotic stresses tolerance in plants. In-depth study and characterization of LEA protein families have been carried out in other plants, but not in upland cotton. The main aim of this rese...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-017-0596-1

    authors: Magwanga RO,Lu P,Kirungu JN,Lu H,Wang X,Cai X,Zhou Z,Zhang Z,Salih H,Wang K,Liu F

    更新日期:2018-01-15 00:00:00

  • Comparison of the accuracy of methods of computational haplotype inference using a large empirical dataset.

    abstract:BACKGROUND:Analyses of genetic data at the level of haplotypes provide increased accuracy and power to infer genotype-phenotype correlations and evolutionary history of a locus. However, empirical determination of haplotypes is expensive and laborious. Therefore, several methods of inferring haplotypes from unphased ge...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-5-22

    authors: Adkins RM

    更新日期:2004-08-03 00:00:00

  • The transcription of MGAT4A glycosyl transferase is increased in white cells of peripheral blood of type 2 diabetes patients.

    abstract:BACKGROUND:Human glycosylase IV is involved in GLUT2 transporter regulation in pancreatic beta cells. A KO of this gene along with a high fat diet in a mice model has been associated with the development of type 2 diabetes (T2D). The aims of this study were to measure and compare the MGAT4A mRNA levels in white blood c...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-8-73

    authors: López-Orduña E,Cruz M,García-Mena J

    更新日期:2007-10-22 00:00:00

  • Comparing self-reported ethnicity to genetic background measures in the context of the Multi-Ethnic Study of Atherosclerosis (MESA).

    abstract:BACKGROUND:Questions remain regarding the utility of self-reported ethnicity (SRE) in genetic and epidemiologic research. It is not clear whether conditioning on SRE provides adequate protection from inflated type I error rates due to population stratification and admixture. We address this question using data obtained...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-12-28

    authors: Divers J,Redden DT,Rice KM,Vaughan LK,Padilla MA,Allison DB,Bluemke DA,Young HJ,Arnett DK

    更新日期:2011-03-04 00:00:00

  • Molecular mechanism of estrogen-mediated neuroprotection in the relief of brain ischemic injury.

    abstract:BACKGROUND:This study aimed to explore the molecular mechanism of estrogen-mediated neuroprotection in the relief of cerebral ischemic injury. The gene expression profiles were downloaded from Gene Expression Omnibus database, and differentially expressed genes (DEGs) were identified using limma package in R software. ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-018-0630-y

    authors: He J,Gao Y,Wu G,Lei X,Zhang Y,Pan W,Yu H

    更新日期:2018-07-20 00:00:00

  • Quantitative trait loci for variation in immune response to a Foot-and-Mouth Disease virus peptide.

    abstract:BACKGROUND:Infectious disease of livestock continues to be a cause of substantial economic loss and has adverse welfare consequences in both the developing and developed world. New solutions to control disease are needed and research focused on the genetic loci determining variation in immune-related traits has the pot...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-11-107

    authors: Leach RJ,Craigmile SC,Knott SA,Williams JL,Glass EJ

    更新日期:2010-12-07 00:00:00

  • PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle.

    abstract:BACKGROUND:Non-synonymous polymorphisms within the prion protein gene (PRNP) influence the susceptibility and incubation time for transmissible spongiform encephalopathies (TSE) in some species such as sheep and humans. In cattle, none of the known polymorphisms within the PRNP coding region has a major influence on su...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-8-15

    authors: Haase B,Doherr MG,Seuberlich T,Drögemüller C,Dolf G,Nicken P,Schiebel K,Ziegler U,Groschup MH,Zurbriggen A,Leeb T

    更新日期:2007-04-16 00:00:00

  • Family-based approaches: design, imputation, analysis, and beyond.

    abstract::Participants in the family-based analysis group at Genetic Analysis Workshop 19 addressed diverse topics, all of which used the family data. Topics addressed included questions of study design and data quality control (QC), genotype imputation to augment available sequence data, and linkage and/or association analyses...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-015-0318-5

    authors: Wijsman EM

    更新日期:2016-02-03 00:00:00

  • The distribution of mitochondrial DNA haplogroup H in southern Iberia indicates ancient human genetic exchanges along the western edge of the Mediterranean.

    abstract:BACKGROUND:The structure of haplogroup H reveals significant differences between the western and eastern edges of the Mediterranean, as well as between the northern and southern regions. Human populations along the westernmost Mediterranean coasts, which were settled by individuals from two continents separated by a re...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-017-0514-6

    authors: Hernández CL,Dugoujon JM,Novelletto A,Rodríguez JN,Cuesta P,Calderón R

    更新日期:2017-05-19 00:00:00

  • Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history.

    abstract:BACKGROUND:The N-acetyltransferase 2 (NAT2) gene plays a crucial role in the metabolism of many drugs and xenobiotics. As it represents a likely target of population-specific selection pressures, we fully sequenced the NAT2 coding region in 97 Mandenka individuals from Senegal, and compared these sequences to extant da...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-9-21

    authors: Sabbagh A,Langaney A,Darlu P,Gérard N,Krishnamoorthy R,Poloni ES

    更新日期:2008-02-27 00:00:00

  • Tissue expression profiles unveil the gene interaction of hepatopancreas, eyestalk, and ovary in the precocious female Chinese mitten crab, Eriocheir sinensis.

    abstract:BACKGROUND:Sexual precocity is a common biological phenomenon in animal species. A large number of precocity individuals were identified in Chinese mitten crab Eriocheir sinensis, which caused huge economic loss annually. However, the underlying genetic basis of precocity in E. sinensis remains unclear to date. RESULT...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/s12863-019-0716-1

    authors: Chen X,Wang J,Hou X,Yue W,Huang S,Wang C

    更新日期:2019-01-25 00:00:00

  • Microsatellites versus single-nucleotide polymorphisms in linkage analysis for quantitative and qualitative measures.

    abstract:BACKGROUND:Genetic maps based on single-nucleotide polymorphisms (SNP) are increasingly being used as an alternative to microsatellite maps. This study compares linkage results for both types of maps for a neurophysiology phenotype and for an alcohol dependence phenotype. Our analysis used two SNP maps on the Illumina ...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-6-S1-S122

    authors: Dunn G,Hinrichs AL,Bertelsen S,Jin CH,Kauwe JS,Suarez BK,Bierut LJ

    更新日期:2005-12-30 00:00:00

  • Reassessment of the function of somatolactin alpha in lipid metabolism using medaka mutant and transgenic strains.

    abstract:BACKGROUND:Somatolactin alpha (SLa) is a fish-specific peptide hormone secreted from the pituitary. In medaka, SLa functions to darken the skin color and lack of SLa makes it pale. Transcription of SLa is enhanced or suppressed when fish are kept in dark or bright conditions, respectively, indicating SLa's important ro...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-13-64

    authors: Sasano Y,Yoshimura A,Fukamachi S

    更新日期:2012-07-24 00:00:00

  • Genome-wide association and systems genetic analyses of residual feed intake, daily feed consumption, backfat and weight gain in pigs.

    abstract:BACKGROUND:Feed efficiency is one of the major components determining costs of animal production. Residual feed intake (RFI) is defined as the difference between the observed and the expected feed intake given a certain production. Residual feed intake 1 (RFI1) was calculated based on regression of individual daily fee...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-15-27

    authors: Do DN,Ostersen T,Strathe AB,Mark T,Jensen J,Kadarmideen HN

    更新日期:2014-02-17 00:00:00

  • Molecular organization and chromosomal localization of 5S rDNA in Amazonian Engystomops (Anura, Leiuperidae).

    abstract:BACKGROUND:For anurans, knowledge of 5S rDNA is scarce. For Engystomops species, chromosomal homeologies are difficult to recognize due to the high level of inter- and intraspecific cytogenetic variation. In an attempt to better compare the karyotypes of the Amazonian species Engystomops freibergi and Engystomops peter...

    journal_title:BMC genetics

    pub_type: 杂志文章

    doi:10.1186/1471-2156-13-17

    authors: Rodrigues DS,Rivera M,Lourenço LB

    更新日期:2012-03-20 00:00:00