RT Journal A1 Tassy, Olivier A1 Dauga, Delphine A1 Daian, Fabrice A1 Sobral, Daniel A1 Robin, François A1 Khoueiry, Pierre A1 Salgado, David A1 Fox, Vanessa A1 Caillol, Danièle A1 Schiappa, Renaud A1 Laporte, Baptiste A1 Rios, Anne A1 Luxardi, Guillaume A1 Kusakabe, Takehiro A1 Joly, Jean-Stéphane A1 Darras, Sébastien A1 Christiaen, Lionel A1 Contensin, Magali A1 Auger, Hélène A1 Lamy, Clément A1 Hudson, Clare A1 Rothbächer, Ute A1 Gilchrist, Michael J. A1 Makabe, Kazuhiro W. A1 Hotta, Kohji A1 Fujiwara, Shigeki A1 Satoh, Nori A1 Satou, Yutaka A1 Lemaire, Patrick T1 The ANISEED database: Digital representation, formalization, and elucidation of a chordate developmental program JF Genome Research JO Genome Research YR 2010 FD October 01 VO 20 IS 10 SP 1459 OP 1468 DO 10.1101/gr.108175.110 UL http://genome.cshlp.org/content/20/10/1459.abstract AB Developmental biology aims to understand how the dynamics of embryonic shapes and organ functions are encoded in linear DNA molecules. Thanks to recent progress in genomics and imaging technologies, systemic approaches are now used in parallel with small-scale studies to establish links between genomic information and phenotypes, often described at the subcellular level. Current model organism databases, however, do not integrate heterogeneous data sets at different scales into a global view of the developmental program. Here, we present a novel, generic digital system, NISEED, and its implementation, ANISEED, to ascidians, which are invertebrate chordates suitable for developmental systems biology approaches. ANISEED hosts an unprecedented combination of anatomical and molecular data on ascidian development. This includes the first detailed anatomical ontologies for these embryos, and quantitative geometrical descriptions of developing cells obtained from reconstructed three-dimensional (3D) embryos up to the gastrula stages. Fully annotated gene model sets are linked to 30,000 high-resolution spatial gene expression patterns in wild-type and experimentally manipulated conditions and to 528 experimentally validated cis-regulatory regions imported from specialized databases or extracted from 160 literature articles. This highly structured data set can be explored via a Developmental Browser, a Genome Browser, and a 3D Virtual Embryo module. We show how integration of heterogeneous data in ANISEED can provide a system-level understanding of the developmental program through the automatic inference of gene regulatory interactions, the identification of inducing signals, and the discovery and explanation of novel asymmetric divisions.