Literature DB >> 16368771

FLOSS: flexible ordered subset analysis for linkage mapping of complex traits.

B L Browning1.   

Abstract

The FLOSS software package is a flexible framework for ordered subset analysis. FLOSS is specifically designed for use with the Merlin linkage analysis package, but FLOSS can be used with any linkage analysis software package that reports NPL Z-scores for each locus and family. When FLOSS is used with the Merlin linkage analysis package, one can use either non-parametric Z-scores or Kong and Cox linear allele sharing model LOD scores. Monte Carlo P-values are calculated using a permutation test with an efficient Besag-Clifford sequential stopping rule. FLOSS also has a flexible tool for assigning family covariate scores from Merlin input files. FLOSS includes user documentation and is written in Java for easy portability. The FLOSS source code is documented and designed to be extensible.

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Year:  2005        PMID: 16368771     DOI: 10.1093/bioinformatics/btk012

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  14 in total

1.  A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins.

Authors:  Jodie N Painter; Gonneke Willemsen; Dale Nyholt; Chantal Hoekstra; David L Duffy; Anjali K Henders; Leanne Wallace; Sue Healey; Lisa A Cannon-Albright; Mark Skolnick; Nicholas G Martin; Dorret I Boomsma; Grant W Montgomery
Journal:  Hum Reprod       Date:  2010-04-08       Impact factor: 6.918

2.  Ordered subset analysis identifies loci influencing lung cancer risk on chromosomes 6q and 12q.

Authors:  Shenying Fang; Susan M Pinney; Joan E Bailey-Wilson; Mariza A de Andrade; Yafang Li; Elena Kupert; Ming You; Ann G Schwartz; Ping Yang; Marshall W Anderson; Christopher I Amos
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2010-10-28       Impact factor: 4.254

3.  Ordered subset linkage analysis based on admixture proportion identifies new linkage evidence for alcohol dependence in African-Americans.

Authors:  Shizhong Han; Joel Gelernter; Henry R Kranzler; Bao-Zhu Yang
Journal:  Hum Genet       Date:  2012-12-13       Impact factor: 4.132

4.  Genome-wide high-density SNP linkage search for glioma susceptibility loci: results from the Gliogene Consortium.

Authors:  Sanjay Shete; Ching C Lau; Richard S Houlston; Elizabeth B Claus; Jill Barnholtz-Sloan; Rose Lai; Dora Il'yasova; Joellen Schildkraut; Siegal Sadetzki; Christoffer Johansen; Jonine L Bernstein; Sara H Olson; Robert B Jenkins; Ping Yang; Nicholas A Vick; Margaret Wrensch; Faith G Davis; Bridget J McCarthy; Eastwood Hon-chiu Leung; Caleb Davis; Rita Cheng; Fay J Hosking; Georgina N Armstrong; Yanhong Liu; Robert K Yu; Roger Henriksson; Beatrice S Melin; Melissa L Bondy
Journal:  Cancer Res       Date:  2011-10-28       Impact factor: 12.701

5.  Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve.

Authors:  Robert B Hinton; Lisa J Martin; Smitha Rame-Gowda; Meredith E Tabangin; Linda H Cripe; D Woodrow Benson
Journal:  J Am Coll Cardiol       Date:  2009-03-24       Impact factor: 24.094

6.  Ordered subsets linkage analysis of antisocial behavior in substance use disorder among participants in the Collaborative Study on the Genetics of Alcoholism.

Authors:  Kristen C Jacobson; Cheryl L Beseler; Jessica Lasky-Su; Stephen V Faraone; Stephen J Glatt; William S Kremen; Michael J Lyons; Ming T Tsuang
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-10-05       Impact factor: 3.568

7.  Evidence for gene-smoking interactions for hearing loss and deafness in Japanese American families.

Authors:  Jia Y Wan; Christina Cataby; Andrew Liem; Emily Jeffrey; Trina M Norden-Krichmar; Deborah Goodman; Stephanie A Santorico; Karen L Edwards
Journal:  Hear Res       Date:  2019-12-24       Impact factor: 3.208

8.  Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.

Authors:  J A Badner; D Koller; T Foroud; H Edenberg; J I Nurnberger; P P Zandi; V L Willour; F J McMahon; J B Potash; M Hamshere; D Grozeva; E Green; G Kirov; I Jones; L Jones; N Craddock; D Morris; R Segurado; M Gill; D Sadovnick; R Remick; P Keck; J Kelsoe; M Ayub; A MacLean; D Blackwood; C-Y Liu; E S Gershon; W McMahon; G J Lyon; R Robinson; J Ross; W Byerley
Journal:  Mol Psychiatry       Date:  2011-07-19       Impact factor: 15.992

9.  Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.

Authors:  J L McCauley; R L Zuvich; Y Bradford; S J Kenealy; N Schnetz-Boutaud; S G Gregory; S L Hauser; J R Oksenberg; D P Mortlock; M A Pericak-Vance; J L Haines
Journal:  Genes Immun       Date:  2009-07-23       Impact factor: 2.676

10.  Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

Authors:  Xiao-Qing Liu; Andrew D Paterson; Peter Szatmari
Journal:  Biol Psychiatry       Date:  2008-07-16       Impact factor: 13.382

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