Literature DB >> 7795601

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome.

J Dubovsky1, V C Sheffield, G M Duyk, J L Weber.   

Abstract

For the purpose of initial screening of the human genome in linkage mapping, two overlapping sets of high quality short tandem repeat polymorphisms (STRPs) which span the autosomes have been assembled. The higher density set contains a total of 363 markers with an average heterozygosity of 79% and an average sex-equal genetic distance between markers of 10.5 cM. The lower density set, which is a subset of the other, contains 156 markers with an average heterozygosity of 80% and an average spacing of 26.5 cM. Tri- and tetranucleotide STRPs comprised 47 and 63%, respectively, of the markers within the higher and lower density sets. Markers within the screening sets were selected to have maximum quality, where quality was defined as a blend of high informativeness, strong amplification under standard PCR conditions, low amplification background, and ease in scoring. The screening sets along with combinations of STRPs which can be amplified and electrophoresed simultaneously are available electronically through anonymous ftp.

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Year:  1995        PMID: 7795601     DOI: 10.1093/hmg/4.3.449

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  23 in total

1.  Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

Authors:  S Goobie; M Popovic; J Morrison; L Ellis; H Ginzberg; G R Boocock; N Ehtesham; C Bétard; C G Brewer; N M Roslin; T J Hudson; K Morgan; T M Fujiwara; P R Durie; J M Rommens
Journal:  Am J Hum Genet       Date:  2001-03-15       Impact factor: 11.025

2.  Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array.

Authors:  Hajime Matsuzaki; Halina Loi; Shoulian Dong; Ya-Yu Tsai; Joy Fang; Jane Law; Xiaojun Di; Wei-Min Liu; Geoffrey Yang; Guoying Liu; Jing Huang; Giulia C Kennedy; Thomas B Ryder; Gregory A Marcus; P Sean Walsh; Mark D Shriver; Jennifer M Puck; Keith W Jones; Rui Mei
Journal:  Genome Res       Date:  2004-03       Impact factor: 9.043

3.  Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Authors:  C Bétard; A Rasquin-Weber; C Brewer; E Drouin; S Clark; A Verner; C Darmond-Zwaig; J Fortin; J Mercier; P Chagnon; T M Fujiwara; K Morgan; A Richter; T J Hudson; G A Mitchell
Journal:  Am J Hum Genet       Date:  2000-05-11       Impact factor: 11.025

4.  Genomewide search for genes influencing percent body fat in Pima Indians: suggestive linkage at chromosome 11q21-q22. Pima Diabetes Gene Group.

Authors:  R A Norman; D B Thompson; T Foroud; W T Garvey; P H Bennett; C Bogardus; E Ravussin
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

5.  Improved set of short-tandem-repeat polymorphisms for screening the human genome.

Authors:  B Yuan; D Vaske; J L Weber; J Beck; V C Sheffield
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

6.  Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q.

Authors:  C D Fenske; S Jeffery; J L Weber; R S Houlston; J V Leonard; P J Lee
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

7.  [A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter].

Authors:  D Bönsch; C-M Schmidt; P Scheer; J Bohlender; C Neumann; A Am Zehnhoff-Dinnesen; T Deufel
Journal:  HNO       Date:  2009-04       Impact factor: 1.284

8.  Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

Authors:  M Piantanida; E Buscarini; C Dellavecchia; A Minelli; A Rossi; L Buscarini; C Danesino
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

9.  [A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].

Authors:  D Bönsch; C M Schmidt; P Scheer; J Bohlender; C Neumann; A am Zehnhoff-Dinnesen; T Deufel
Journal:  HNO       Date:  2008-02       Impact factor: 1.284

10.  A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.

Authors:  S C Wildenberg; W S Oetting; C Almodóvar; M Krumwiede; J G White; R A King
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

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