Literature DB >> 16894467

Establishment of the 1st International Genetic Reference Panel for Factor V Leiden, human gDNA.

Elaine Gray1, J Ross Hawkins, Marion Morrison, Malcolm Hawkins, Ed Byrne, Steve Kitchen, Ian Jennings, Mike Makris, F Eric Preston, Paul Metcalfe.   

Abstract

Forty-one laboratories participated in an international collaborative study to assess the suitability of a panel of three genomic DNA samples as the 1st International Genetic Reference Panel for the Factor V Leiden (FVL) variant. The code numbers of the materials were 03/254 (FV wild type), 03/260 (FVL homozygote) and 03/248 (FVL heterozygote). The participants evaluated the panel against their in-house controls which were known patient samples and commercial controls. In total, 859 genotype tests were carried out on the panel, with an error rate of 0.7%. The errors were not related to specific samples of the panel or to any specific techniques. The findings of this study have indicated that this panel is suitable to be used as a reference material for genotyping of factor V Leiden. It was therefore recommended that the three genomic DNA samples be established as the 1st International Genetic Reference Panel for Factor V Leiden, Human gDNA, 04/224. This recommendation was approved by the Scientific and Standardization Committee (SSC) of the ISTH (International Society on Thrombosis and Haemostasis) in June 2004 and the Expert Committee on Biological Standardization (ECBS) of the World Health Organization (WHO) in November 2004.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16894467

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  4 in total

1.  Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome.

Authors:  Malcolm Hawkins; Jennifer Boyle; Kathleen E Wright; Rob Elles; Simon C Ramsden; Anna O'Grady; Michael Sweeney; David E Barton; Trent Burgess; Melanie Moore; Chris Burns; Glyn Stacey; Elaine Gray; Paul Metcalfe; J Ross Hawkins
Journal:  Eur J Hum Genet       Date:  2010-08-25       Impact factor: 4.246

2.  Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes.

Authors:  Jennifer Boyle; Malcolm Hawkins; David E Barton; Karen Meaney; Miriam Guitart; Anna O'Grady; Simon Tobi; Simon C Ramsden; Rob Elles; Elaine Gray; Paul Metcalfe; J Ross Hawkins
Journal:  Eur J Hum Genet       Date:  2011-05-18       Impact factor: 4.246

3.  Evolving methods for single nucleotide polymorphism detection: Factor V Leiden mutation detection.

Authors:  Herin Oh; Cassandra L Smith
Journal:  J Clin Lab Anal       Date:  2011       Impact factor: 2.352

4.  Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia.

Authors:  Rola F Turki; Mourad Assidi; Huda A Banni; Hanan A Zahed; Sajjad Karim; Hans-Juergen Schulten; Muhammad Abu-Elmagd; Abdulrahim A Rouzi; Osama Bajouh; Hassan S Jamal; Mohammed H Al-Qahtani; Adel M Abuzenadah
Journal:  BMC Med Genet       Date:  2016-10-10       Impact factor: 2.103

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.