Literature DB >> 7920657

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping.

P W Reed1, J L Davies, J B Copeman, S T Bennett, S M Palmer, L E Pritchard, S C Gough, Y Kawaguchi, H J Cordell, K M Balfour.   

Abstract

To facilitate large-scale genetic mapping of the human genome, we have developed chromosome-specific sets of microsatellite marker loci suitable for use with a fluorescence-based automated DNA fragment analyser. We present 254 dinucleotide repeat marker loci (80% from the Généthon genetic linkage map) arranged into 39 sets, covering all 22 autosomes and the X chromosome. The average distance between adjacent markers is 13 centiMorgans, and less than 4% of the genome lies more than 20 cM from the nearest marker. Each set of microsatellites consists of up to nine marker loci, with allele size ranges that do not overlap. We selected marker loci on the basis of their reliability in the polymerase chain reaction, polymorphism content, map position and the accuracy with which alleles can be scored automatically by the Genotyper program.

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Year:  1994        PMID: 7920657     DOI: 10.1038/ng0794-390

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  72 in total

1.  Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate loci.

Authors:  C D Veal; R L Clough; R C Barber; S Mason; D Tillman; B Ferry; A B Jones; M Ameen; N Balendran; S H Powis; A D Burden; J N Barker; R C Trembath
Journal:  J Med Genet       Date:  2001-01       Impact factor: 6.318

2.  A novel X-linked dominant condition: X-linked congenital isolated ptosis.

Authors:  T F McMullan; A R Collins; A G Tyers; D O Robinson
Journal:  Am J Hum Genet       Date:  2000-03-14       Impact factor: 11.025

Review 3.  Gene mapping by linkage and association analysis.

Authors:  R E March
Journal:  Mol Biotechnol       Date:  1999-12-01       Impact factor: 2.695

4.  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

5.  Genomewide scans of complex human diseases: true linkage is hard to find.

Authors:  J Altmüller; L J Palmer; G Fischer; H Scherb; M Wjst
Journal:  Am J Hum Genet       Date:  2001-09-14       Impact factor: 11.025

6.  Loss of heterozygosity analysis using whole genome amplification, cell sorting, and fluorescence-based PCR.

Authors:  T G Paulson; P C Galipeau; B J Reid
Journal:  Genome Res       Date:  1999-05       Impact factor: 9.043

7.  Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism.

Authors:  Jan Fullerton; Matthew Cubin; Hemant Tiwari; Chenxi Wang; Amarjit Bomhra; Stuart Davidson; Sue Miller; Christopher Fairburn; Guy Goodwin; Michael C Neale; Simon Fiddy; Richard Mott; David B Allison; Jonathan Flint
Journal:  Am J Hum Genet       Date:  2003-02-20       Impact factor: 11.025

8.  Comparison of genome screens for two independent cohorts provides replication of suggestive linkage of bone mineral density to 3p21 and 1p36.

Authors:  S G Wilson; P W Reed; A Bansal; M Chiano; M Lindersson; M Langdown; R L Prince; D Thompson; E Thompson; M Bailey; P W Kleyn; P Sambrook; M M Shi; T D Spector
Journal:  Am J Hum Genet       Date:  2002-12-11       Impact factor: 11.025

Review 9.  Genetics of hypertension. Therapeutic implications.

Authors:  S O'Byrne; M Caulfield
Journal:  Drugs       Date:  1998-08       Impact factor: 9.546

Review 10.  Mapping the mouse genome: current status and future prospects.

Authors:  W F Dietrich; N G Copeland; D J Gilbert; J C Miller; N A Jenkins; E S Lander
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-21       Impact factor: 11.205

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