Literature DB >> 9634505

PedCheck: a program for identification of genotype incompatibilities in linkage analysis.

J R O'Connell1, D E Weeks.   

Abstract

Prior to performance of linkage analysis, elimination of all Mendelian inconsistencies in the pedigree data is essential. Often, identification of erroneous genotypes by visual inspection can be very difficult and time consuming. In fact, sometimes the errors are not recognized until the stage of running linkage-analysis software. The effort then required to find the erroneous genotypes and to cross-reference pedigree and marker data that may have been recoded and renumbered can be not only tedious but also quite daunting, in the case of very large pedigrees. We have implemented four error-checking algorithms in a new computer program, PedCheck, which will assist researchers in identifying all Mendelian inconsistencies in pedigree data and will provide them with useful and detailed diagnostic information to help resolve the errors. Our program, which uses many of the algorithms implemented in VITESSE, handles large data sets quickly and efficiently, accepts a variety of input formats, and offers various error-checking algorithms that match the subtlety of the pedigree error. These algorithms range from simple parent-offspring-compatibility checks to a single-locus likelihood-based statistic that identifies and ranks the individuals most likely to be in error. We use various real data sets to illustrate the power and effectiveness of our program.

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Mesh:

Year:  1998        PMID: 9634505      PMCID: PMC1377228          DOI: 10.1086/301904

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  15 in total

1.  A test statistic to detect errors in sib-pair relationships.

Authors:  M Ehm; M Wagner
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

2.  Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE.

Authors:  K Lange; D Weeks; M Boehnke
Journal:  Genet Epidemiol       Date:  1988       Impact factor: 2.135

3.  Efficient computation of lod scores: genotype elimination, genotype redefinition, and hybrid maximum likelihood algorithms.

Authors:  K Lange; D E Weeks
Journal:  Ann Hum Genet       Date:  1989-01       Impact factor: 1.670

4.  An algorithm for automatic genotype elimination.

Authors:  K Lange; T M Goradia
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

5.  Detecting marker inconsistencies in human gene mapping.

Authors:  J Ott
Journal:  Hum Hered       Date:  1993 Jan-Feb       Impact factor: 0.444

6.  Evaluating pedigree data. II. Identifying the cause of error in families with inconsistencies.

Authors:  G M Lathrop; J W Huntsman; A B Hooper; R H Ward
Journal:  Hum Hered       Date:  1983       Impact factor: 0.444

7.  Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping.

Authors:  G M Lathrop; A B Hooper; J W Huntsman; R H Ward
Journal:  Am J Hum Genet       Date:  1983-03       Impact factor: 11.025

8.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

9.  Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

Authors:  G M Lathrop; J M Lalouel; R L White
Journal:  Genet Epidemiol       Date:  1986       Impact factor: 2.135

10.  The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance.

Authors:  J R O'Connell; D E Weeks
Journal:  Nat Genet       Date:  1995-12       Impact factor: 38.330

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  931 in total

1.  An optimal algorithm for automatic genotype elimination.

Authors:  J R O'Connell; D E Weeks
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Authors:  J A Douglas; M Boehnke; K Lange
Journal:  Am J Hum Genet       Date:  2000-03-28       Impact factor: 11.025

3.  High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12.

Authors:  R H Duerr; M M Barmada; L Zhang; R Pfützer; D E Weeks
Journal:  Am J Hum Genet       Date:  2000-04-03       Impact factor: 11.025

4.  A genomic scan of families with prostate cancer identifies multiple regions of interest.

Authors:  M Gibbs; J L Stanford; G P Jarvik; M Janer; M Badzioch; M A Peters; E L Goode; S Kolb; L Chakrabarti; M Shook; R Basom; E A Ostrander; L Hood
Journal:  Am J Hum Genet       Date:  2000-05-19       Impact factor: 11.025

5.  A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.

Authors:  A Leal; B Morera; D Heuss; C Kayser; M Berghoff; R Villegas; E Hernández; M Méndez; H C Hennies; B Neundörfer; R Barrantes; A Reis; B Rautenstrauss
Journal:  Am J Hum Genet       Date:  2000-12-07       Impact factor: 11.025

6.  The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn disease.

Authors:  M Parkes; M M Barmada; J Satsangi; D E Weeks; D P Jewell; R H Duerr
Journal:  Am J Hum Genet       Date:  2000-11-10       Impact factor: 11.025

7.  Identification and analysis of error types in high-throughput genotyping.

Authors:  K R Ewen; M Bahlo; S A Treloar; D F Levinson; B Mowry; J W Barlow; S J Foote
Journal:  Am J Hum Genet       Date:  2000-08-02       Impact factor: 11.025

8.  Genomewide linkage analysis of celiac disease in Finnish families.

Authors:  Jianjun Liu; Suh-Hang Juo; Päivi Holopainen; Joseph Terwilliger; Xiaomei Tong; Adina Grunn; Miguel Brito; Peter Green; Kirsi Mustalahti; Markku Mäki; T Conrad Gilliam; Jukka Partanen
Journal:  Am J Hum Genet       Date:  2001-11-19       Impact factor: 11.025

9.  Mutation patterns at dinucleotide microsatellite loci in humans.

Authors:  Qing-Yang Huang; Fu-Hua Xu; Hui Shen; Hong-Yi Deng; Yong-Jun Liu; Yao-Zhong Liu; Jin-Long Li; Robert R Recker; Hong-Wen Deng
Journal:  Am J Hum Genet       Date:  2002-01-15       Impact factor: 11.025

10.  Detection and integration of genotyping errors in statistical genetics.

Authors:  Eric Sobel; Jeanette C Papp; Kenneth Lange
Journal:  Am J Hum Genet       Date:  2002-01-08       Impact factor: 11.025

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