Literature DB >> 16326825

Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs.

E Rampersaud1, W K Scott, E R Hauser, M C Speer.   

Abstract

Multipoint linkage analysis in complex diseases requires the use of fast algorithms that can handle many markers and a large number of moderately sized pedigrees with unknown mode of inheritance. This need has led to the development of several competitive software programs. We recently completed a genomic screen of neural tube defects using GENEHUNTER-PLUS and the more recent ALLEGRO. The ALLEGRO software was found to offer expanded power for linkage studies, particularly for childhood onset diseases like neural tube defects, though the results must be treated with caution.

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Year:  2005        PMID: 16326825      PMCID: PMC1735966          DOI: 10.1136/jmg.2005.032029

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  3 in total

1.  Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum.

Authors:  A B Ekici; D Hilfinger; M Jatzwauk; C T Thiel; D Wenzel; I Lorenz; E Boltshauser; T W Goecke; G Staatz; D J Morris-Rosendahl; H Sticht; U Hehr; A Reis; A Rauch
Journal:  Mol Syndromol       Date:  2010-09-14

2.  NEK1 mutations cause short-rib polydactyly syndrome type majewski.

Authors:  Christian Thiel; Kristin Kessler; Andreas Giessl; Arno Dimmler; Stavit A Shalev; Sigrun von der Haar; Martin Zenker; Diana Zahnleiter; Hartmut Stöss; Ernst Beinder; Rami Abou Jamra; Arif B Ekici; Nadja Schröder-Kress; Thomas Aigner; Thomas Kirchner; André Reis; Johann H Brandstätter; Anita Rauch
Journal:  Am J Hum Genet       Date:  2011-01-07       Impact factor: 11.025

3.  Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.

Authors:  Kristen L Deak; Deborah G Siegel; Timothy M George; Simon Gregory; Allison Ashley-Koch; Marcy C Speer
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2008-10
  3 in total

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