Literature DB >> 8330881

A procedure for combining two-point lod scores into a summary multipoint map.

D Curtis1, H Gurling.   

Abstract

Multipoint linkage analysis can be extremely demanding in terms of computer time and memory, and these requirements rise exponentially with the number of markers used. A method is described for producing a rapid approximation to a multipoint analysis from the supplied results of two-point analyses with each marker. The method depends on regarding the lod scores as if they were obtained from a number of independent phase-known meioses, and making estimates concerning the proportion of all meioses which are likely to be informative for each marker. It then becomes possible to estimate the amount of information from each marker or pair of markers which is independent of information from other markers. The lod scores arising from independent contributions may then be summed to approximate the true multipoint lod score. The method has been implemented in a computer program called FASTMAP which is freely available. It has been tested on a variety of simulated and real data. In most circumstances it performs well, with a high correlation between the estimated and true multipoint lod score and little bias. However occasionally the results of the estimate deviate markedly from the multipoint lod score, especially at map positions very close to the markers. The overall usefulness of the method will therefore need to be further evaluated, but it does seem adequate at least for building exclusion maps and carrying out preliminary and exploratory analyses.

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Year:  1993        PMID: 8330881     DOI: 10.1159/000154174

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  16 in total

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2.  Efficient multipoint mapping: making use of dominant repulsion-phase markers.

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3.  Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genes.

Authors:  S J Hasstedt; M Hoffman; M F Leppert; S C Elbein
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4.  A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3.

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5.  GRAMA: genetic mapping analysis of temperature gradient capillary electrophoresis data.

Authors:  Philip M Maher; Hui-Hsien Chou; Elizabeth Hahn; Tsui-Jung Wen; Patrick S Schnable
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Review 6.  Software for genetic linkage analysis: an update.

Authors:  S P Bryant
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7.  Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.

Authors:  F V Elmslie; M P Williamson; M Rees; M Kerr; M J Kjeldsen; K A Pang; A Sundqvist; M L Friis; A Richens; D Chadwick; W P Whitehouse; R M Gardiner
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

Review 8.  Programs, databases, and expert systems for human geneticists--a survey.

Authors:  C Fischer; S Schweigert; C Spreckelsen; F Vogel
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

Review 9.  Genetics of diabetic nephropathy in the Pima Indians.

Authors:  G Imperatore; W C Knowler; R G Nelson; R L Hanson
Journal:  Curr Diab Rep       Date:  2001-12       Impact factor: 4.810

10.  Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Authors:  W P Whitehouse; M Rees; D Curtis; A Sundqvist; K Parker; E Chung; D Baralle; R M Gardiner
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

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