Literature DB >> 8023845

Rapid and efficient resolution of parentage by amplification of short tandem repeats.

R L Alford1, H A Hammond, I Coto, C T Caskey.   

Abstract

Short tandem repeat (STR) loci are highly informative polymorphic loci that are gaining popularity for identity testing. We have conducted parentage testing by using nine STR loci on 50 paternity trios that had been previously tested using VNTR loci. These nine unlinked STR loci are amplified in three multiplex reactions and, when examined for genetic informativeness, provide a combined average power of exclusion of 99.73% (Caucasian data). The informative value of the selected loci is based on extensive STR typing of four racial/ethnic populations. In 37 of the 50 cases, paternity could not be excluded by any of the loci. In the remaining 13 cases, paternity was excluded by at least two of the STR markers. The probability of paternity calculated for the alleged father of each matching trio was > 99% in 36 of the 37 inclusion cases. All data agreed with the results reported using VNTR loci and conventional Southern technology. Our studies validate the use of DNA typing with STR loci for parentage testing, thus providing an accurate, highly sensitive, and rapid assay.

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Year:  1994        PMID: 8023845      PMCID: PMC1918214     

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


  19 in total

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Authors:  R Chakraborty
Journal:  Genetics       Date:  1981-06       Impact factor: 4.562

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Journal:  Genomics       Date:  1992-02       Impact factor: 5.736

4.  Biostatistical evaluation of evidence from continuous allele frequency distribution deoxyribonucleic acid (DNA) probes in reference to disputed paternity and identity.

Authors:  J W Morris; A I Sanda; J Glassberg
Journal:  J Forensic Sci       Date:  1989-11       Impact factor: 1.832

5.  Hypervariability of simple sequences as a general source for polymorphic DNA markers.

Authors:  D Tautz
Journal:  Nucleic Acids Res       Date:  1989-08-25       Impact factor: 16.971

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Journal:  Nucleic Acids Res       Date:  1988-03-11       Impact factor: 16.971

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Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Mar 7-13       Impact factor: 49.962

8.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

Authors:  J L Weber; P E May
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

9.  Allele frequency distribution of two highly polymorphic DNA sequences in three ethnic groups and its application to the determination of paternity.

Authors:  M Baird; I Balazs; A Giusti; L Miyazaki; L Nicholas; K Wexler; E Kanter; J Glassberg; F Allen; P Rubinstein
Journal:  Am J Hum Genet       Date:  1986-10       Impact factor: 11.025

10.  Evaluation of 13 short tandem repeat loci for use in personal identification applications.

Authors:  H A Hammond; L Jin; Y Zhong; C T Caskey; R Chakraborty
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

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  12 in total

1.  Analysis of short tandem repeat polymorphisms by electrospray ion trap mass spectrometry.

Authors:  S Hahner; A Schneider; A Ingendoh; J Mosner
Journal:  Nucleic Acids Res       Date:  2000-09-15       Impact factor: 16.971

2.  Extraction of high quality DNA from bloodstains using diatoms.

Authors:  S Günther; J Herold; D Patzelt
Journal:  Int J Legal Med       Date:  1995       Impact factor: 2.686

3.  Evaluation of new primers for CSF1PO.

Authors:  K Yoshida; K Sekiguchi; K Kasai; H Sato; S Seta; G F Sensabaugh
Journal:  Int J Legal Med       Date:  1997       Impact factor: 2.686

4.  Technical note: multi-alleles at the DYS385ab locus with high frequency in a Han Chinese population from southwestern China.

Authors:  Jiewen Fu; Shangyi Fu; Shiqiang Yin; Jingliang Cheng; Xiaoyan Liu; Zeming Jin; Tao He; Junjiang Fu
Journal:  Int J Legal Med       Date:  2021-04-12       Impact factor: 2.686

5.  Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.

Authors:  Koji M Nishiguchi; James S Friedman; Michael A Sandberg; Anand Swaroop; Eliot L Berson; Thaddeus P Dryja
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-09       Impact factor: 11.205

6.  Pitfalls of paternity testing based solely on PCR typing of minisatellites and microsatellites.

Authors:  S D Pena
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

7.  Population data for the STR systems HumTH01, HumVWA and FES/FPS in a population sample from lower Franconia.

Authors:  S Günther; D Patzelt
Journal:  Int J Legal Med       Date:  1996       Impact factor: 2.686

8.  Gonadal mosaicism for incontinentia pigmenti in a healthy male.

Authors:  T T Kirchman; M L Levy; R A Lewis; M H Kanzler; D L Nelson; A E Scheuerle
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

9.  Application of microsatellite loci on the chromosome X for rapid prenatal detection of the chromosome X numerical abnormalities.

Authors:  Kristina Crkvenac Gornik; Zorana Grubić; Katarina Stingl; Ivana Tonković Durisević; Davor Begović
Journal:  Croat Med J       Date:  2011-06       Impact factor: 1.351

10.  A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Authors:  D Lorenzetti; D Pareyson; A Sghirlanzoni; B B Roa; N E Abbas; M Pandolfo; S Di Donato; J R Lupski
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

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