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Translating multi-omics into healthcare: requisites for scalable and equitable implementation.

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Title: Translating multi-omics into healthcare: requisites for scalable and equitable implementation.
Authors: Tumiene B; Faculty of Medicine, Institute of Biomedical Sciences, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania., Adams DR; National Human Genome Research Institute, National Institutes of Health, Bethesda, USA., Allaway R; Sage Bionetworks, Seattle, USA., Barrero MJ; Institute of Rare Diseases Research (IIER), Spanish National Institute of Health Carlos III (ISCIII), Madrid, Spain., Chan CH; Sanford Research, Sioux Falls, USA., Faundes V; Laboratorio de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile., Fear VS; The Kids Research Institute Australia, Nedlands, Australia., Glezer P; Chan Zuckerberg Initiative, Redwood City, CA, USA., Fuchs C; EURORDIS, Rare Diseases Europe, Paris, France., Groza T; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.; KK Women's and Children's Hospital, Singapore, Singapore.; Rare Care Centre, Perth Children's Hospital and Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Subiaco, Australia.; Agency for Science, Technology and Research (A*STAR), Bioinformatics Institute (BII), Singapore, Singapore., Houwink EJF; Department of Family Medicine, Mayo Clinic, Rochester, MN, USA., Jamuar SS; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.; KK Women's and Children's Hospital, Singapore, Singapore., Letinturier MCV; IRDiRC Scientific Secretariat, French National Institute of Health and Medical Research (Inserm), Ivry-sur-Seine, France., Lomash RM; National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Maryland, USA., Puri RD; Sir Ganga Ram Hospital, New Delhi, India., Reichardt JKV; Australian Institute of Tropical Health and Medicine, James Cook University, Douglas, Australia., Mehrian-Shai R; The Scojen Institute for Synthetic Biology, Reichman University, Herzliya, Israel., van der Westhuizen FH; Biomedical and Molecular Metabolism Research (BioMMet), North-West University, Potchefstroom, South Africa., Varshney GK; Genes and Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, USA., Yamamoto S; Baylor College of Medicine, Houston, USA., Baynam G; Rare Care Centre, Perth Children's Hospital and Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Subiaco, Australia. gareth.baynam@health.wa.gov.au.
Source: Human genomics [Hum Genomics] 2026 Mar 25; Vol. 20 (1). Date of Electronic Publication: 2026 Mar 25.
Publication Type: Journal Article; Review
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364 (Electronic) Linking ISSN: 14739542 NLM ISO Abbreviation: Hum Genomics Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Translating multi-omics into healthcare: requisites for scalable and equitable implementation.
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  Data: <searchLink fieldCode="AU" term="%22Tumiene+B%22">Tumiene B</searchLink>; Faculty of Medicine, Institute of Biomedical Sciences, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania.<br /><searchLink fieldCode="AU" term="%22Adams+DR%22">Adams DR</searchLink>; National Human Genome Research Institute, National Institutes of Health, Bethesda, USA.<br /><searchLink fieldCode="AU" term="%22Allaway+R%22">Allaway R</searchLink>; Sage Bionetworks, Seattle, USA.<br /><searchLink fieldCode="AU" term="%22Barrero+MJ%22">Barrero MJ</searchLink>; Institute of Rare Diseases Research (IIER), Spanish National Institute of Health Carlos III (ISCIII), Madrid, Spain.<br /><searchLink fieldCode="AU" term="%22Chan+CH%22">Chan CH</searchLink>; Sanford Research, Sioux Falls, USA.<br /><searchLink fieldCode="AU" term="%22Faundes+V%22">Faundes V</searchLink>; Laboratorio de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Fear+VS%22">Fear VS</searchLink>; The Kids Research Institute Australia, Nedlands, Australia.<br /><searchLink fieldCode="AU" term="%22Glezer+P%22">Glezer P</searchLink>; Chan Zuckerberg Initiative, Redwood City, CA, USA.<br /><searchLink fieldCode="AU" term="%22Fuchs+C%22">Fuchs C</searchLink>; EURORDIS, Rare Diseases Europe, Paris, France.<br /><searchLink fieldCode="AU" term="%22Groza+T%22">Groza T</searchLink>; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.; KK Women's and Children's Hospital, Singapore, Singapore.; Rare Care Centre, Perth Children's Hospital and Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Subiaco, Australia.; Agency for Science, Technology and Research (A*STAR), Bioinformatics Institute (BII), Singapore, Singapore.<br /><searchLink fieldCode="AU" term="%22Houwink+EJF%22">Houwink EJF</searchLink>; Department of Family Medicine, Mayo Clinic, Rochester, MN, USA.<br /><searchLink fieldCode="AU" term="%22Jamuar+SS%22">Jamuar SS</searchLink>; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.; KK Women's and Children's Hospital, Singapore, Singapore.<br /><searchLink fieldCode="AU" term="%22Letinturier+MCV%22">Letinturier MCV</searchLink>; IRDiRC Scientific Secretariat, French National Institute of Health and Medical Research (Inserm), Ivry-sur-Seine, France.<br /><searchLink fieldCode="AU" term="%22Lomash+RM%22">Lomash RM</searchLink>; National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Puri+RD%22">Puri RD</searchLink>; Sir Ganga Ram Hospital, New Delhi, India.<br /><searchLink fieldCode="AU" term="%22Reichardt+JKV%22">Reichardt JKV</searchLink>; Australian Institute of Tropical Health and Medicine, James Cook University, Douglas, Australia.<br /><searchLink fieldCode="AU" term="%22Mehrian-Shai+R%22">Mehrian-Shai R</searchLink>; The Scojen Institute for Synthetic Biology, Reichman University, Herzliya, Israel.<br /><searchLink fieldCode="AU" term="%22van+der+Westhuizen+FH%22">van der Westhuizen FH</searchLink>; Biomedical and Molecular Metabolism Research (BioMMet), North-West University, Potchefstroom, South Africa.<br /><searchLink fieldCode="AU" term="%22Varshney+GK%22">Varshney GK</searchLink>; Genes and Human Disease Research Program, Oklahoma Medical Research Foundation, Oklahoma City, USA.<br /><searchLink fieldCode="AU" term="%22Yamamoto+S%22">Yamamoto S</searchLink>; Baylor College of Medicine, Houston, USA.<br /><searchLink fieldCode="AU" term="%22Baynam+G%22">Baynam G</searchLink>; Rare Care Centre, Perth Children's Hospital and Western Australian Register of Developmental Anomalies, King Edward Memorial Hospital, Subiaco, Australia. gareth.baynam@health.wa.gov.au.
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  Data: <searchLink fieldCode="JN" term="%22101202210%22">Human genomics</searchLink> [Hum Genomics] 2026 Mar 25; Vol. 20 (1). <i>Date of Electronic Publication: </i>2026 Mar 25.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101202210 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1479-7364 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214739542%22">14739542 </searchLink><i>NLM ISO Abbreviation: </i>Hum Genomics <i>Subsets: </i>MEDLINE
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