<p>Many human diseases are the result of early developmental defects. As most paediatric diseases and disorders are rare, children are critically underrepresented in research. Functional genomics studies primarily rely on adult tissues and lack critical cell states in specific developmental windows. In parallel, little is known about the conservation of developmental programmes across non-human primate (NHP) species, with implications for human evolution. Here we introduce the developmental Genotype-Tissue Expression (dGTEx) projects, which span humans and NHPs and aim to integrate gene expression, regulation and genetics data across development and species. The dGTEx cohort will consist of 74 tissue sites across 120 human donors from birth to adulthood, and developmentally matched NHP age groups, with additional prenatal and adult animals, with 126 rhesus macaques (<i>Macaca mulatta</i>) and 72 common marmosets (<i>Callithrix jacchus</i>). The data will comprise whole-genome sequencing, extensive bulk, single-cell and spatial gene expression profiles, and chromatin accessibility data across tissues and development. Through community engagement and donor diversity, the human dGTEx study seeks to address disparities in genomic research. Thus, dGTEx will provide a reference human and NHP dataset and tissue bank, enabling research into developmental changes in expression and gene regulation, childhood disorders and the effect of genetic variation on development.</p>

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The human and non-human primate developmental GTEx projects

  • Tim H. H. Coorens,
  • Amy Guillaumet-Adkins,
  • Rothem Kovner,
  • Rebecca L. Linn,
  • Victoria H. J. Roberts,
  • Amrita Sule,
  • Patrick M. Van Hoose,
  • Thomas Bell,
  • Thomas Blanchard,
  • Raquel Hernandez,
  • Rebecca Linn,
  • Deanne Taylor,
  • Melissa VonDran,
  • Taha M. Ahooyi,
  • Danette Beitra,
  • Anas Bernieh,
  • Meghan Delaney,
  • Melissa Faith,
  • Emmanouel Fattahi,
  • Dana Footer,
  • Michelle Gilbert,
  • Simoné Guambaña,
  • Sam Gulino,
  • Jade Hanson,
  • Emilie Hattrell,
  • Casie Heinemann,
  • Joseph Kreeb,
  • Daniel Leino,
  • Laurel Mcdevitt,
  • Abigail Palmieri,
  • Mary Pfeiffer,
  • Gloria Pryhuber,
  • Chrisopher Rossi,
  • Immanuel Rasool,
  • Russell Roberts,
  • Ahmad Salehi,
  • Emmitt A. Savannah,
  • Kristen Stachowicz,
  • David Stokes,
  • Lawrence Suplee,
  • Patrick Van Hoose,
  • Benjamin J. Wilkins,
  • Schawnte’ Williams-Taylor,
  • Shiping Zhang,
  • Kristin G. Ardlie,
  • Gad Getz,
  • Tuuli Lappalainen,
  • Stephen B. Montgomery,
  • François Aguet,
  • Lisa Anderson,
  • Brad Bernstein,
  • Abhishek Choudhary,
  • Laura Domenech,
  • Elizabeth Gaskell,
  • Matthew Johnson,
  • Qiuyue Liu,
  • Andrew R. Marderstein,
  • Jared Nedzel,
  • Joseph Okonda,
  • Evin M. Padhi,
  • MaryKate Rosano,
  • Andrew J. C. Russell,
  • Brady Walker,
  • Nenad Sestan,
  • Mark Gerstein,
  • Aleksandar Milosavljevic,
  • Beatrice Borsari,
  • Hyesun Cho,
  • Declan Clarke,
  • Ashley Deveau,
  • Timur Galeev,
  • Kevin Gobeske,
  • Irbaz Hameed,
  • Anita Huttner,
  • Matthew Jensen,
  • Yunzhe Jiang,
  • Jiaqi Li,
  • Jia Liu,
  • Yuting Liu,
  • Jay Ma,
  • Shrikant Mane,
  • Ran Meng,
  • Anandita Nadkarni,
  • Pengyu Ni,
  • Saejeong Park,
  • Varduhi Petrosyan,
  • Sirisha Pochareddy,
  • Iva Salamon,
  • Yan Xia,
  • Chris Yates,
  • Menglei Zhang,
  • Hongyu Zhao,
  • Donald F. Conrad,
  • Guoping Feng,
  • Fritzie Brady,
  • Magalie Boucher,
  • Lucia Carbone,
  • Jenna Castro,
  • Ricardo del Rosario,
  • Madison Held,
  • Jon Hennebold,
  • Ariah Lacey,
  • Anne Lewis,
  • Ana Cristina Lima,
  • Eisa Mahyari,
  • Samantha Moore,
  • Mariam Okhovat,
  • Victoria Roberts,
  • Samia Silva de Castro,
  • Brady Wessel,
  • Heather Zaniewski,
  • Qiangge Zhang,
  • Alexander Arguello,
  • Jacob J. Baroch,
  • Jyoti Dayal,
  • Adam Felsenfeld,
  • John V. Ilekis,
  • Sheethal Jose,
  • Nicole C. Lockhart,
  • Daniel Miller,
  • Mollie Minear,
  • Melissa Parisi,
  • Amanda Price,
  • Erin Ramos,
  • Sige Zou

摘要

Many human diseases are the result of early developmental defects. As most paediatric diseases and disorders are rare, children are critically underrepresented in research. Functional genomics studies primarily rely on adult tissues and lack critical cell states in specific developmental windows. In parallel, little is known about the conservation of developmental programmes across non-human primate (NHP) species, with implications for human evolution. Here we introduce the developmental Genotype-Tissue Expression (dGTEx) projects, which span humans and NHPs and aim to integrate gene expression, regulation and genetics data across development and species. The dGTEx cohort will consist of 74 tissue sites across 120 human donors from birth to adulthood, and developmentally matched NHP age groups, with additional prenatal and adult animals, with 126 rhesus macaques (Macaca mulatta) and 72 common marmosets (Callithrix jacchus). The data will comprise whole-genome sequencing, extensive bulk, single-cell and spatial gene expression profiles, and chromatin accessibility data across tissues and development. Through community engagement and donor diversity, the human dGTEx study seeks to address disparities in genomic research. Thus, dGTEx will provide a reference human and NHP dataset and tissue bank, enabling research into developmental changes in expression and gene regulation, childhood disorders and the effect of genetic variation on development.