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BMC Pregnancy and Childbirth

, 11:71

First Online: 12 October 2011Received: 15 April 2011Accepted: 12 October 2011

Abstract

Preterm birth is the leading cause of neonatal mortality and perinatal morbidity. The etiology of preterm is multi-factorial and still unclear. As evidence increases for a genetic contribution to PTB, so does the need to explore genomics, transcriptomics, proteomics and metabolomics in its study. This review suggests research guidelines for the conduct of high throughput systems biology investigations into preterm birth with the expectation that this will facilitate the sharing of samples and data internationally through consortia, generating the power needed to study preterm birth using integrated -omics- technologies. The issues to be addressed include: 1 integrated -omics- approaches, 2 phenotyping, 3 sample collection, 4 data management-integrative databases, 5 international consortia and 6 translational feasibility. This manuscript is the product of discussions initiated by the -Omics- Working Group at the Preterm Birth International Collaborative Meeting held at the World Health Organization, Geneva, Switzerland in April 2009.

Electronic supplementary materialThe online version of this article doi:10.1186-1471-2393-11-71 contains supplementary material, which is available to authorized users.

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Author: Sara Gracie - Craig Pennell - Gunvor Ekman-Ordeberg - Stephen Lye - James McManaman - Scott Williams - Lyle Palmer - Mauree

Source: https://link.springer.com/







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