A bioimage informatics platform for high-throughput embryo phenotyping

被引:8
|
作者
Brown, James M. [1 ]
Horner, Neil R. [1 ]
Lawson, Thomas N.
Fiegel, Tanja
Greenaway, Simon
Morgan, Hugh
Ring, Natalie
Santos, Luis
Sneddon, Duncan
Teboul, Lydia
Vibert, Jennifer
Yaikhom, Gagarine
Westerberg, Henrik [2 ]
Mallon, Ann-Marie [3 ]
机构
[1] MRC Harwell Inst, Harwell Campus, Didcot OX11 0RD, Oxon, England
[2] MRC Harwell Inst, Bioimage Informat BioComp, Didcot, Oxon, England
[3] MRC Harwell Inst, BioComp, Didcot, Oxon, England
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
bioimage informatics; image processing; embryonic phenotyping; automated analysis; high-throughput; software tools; MAMMALIAN GENE-FUNCTION; EXPERIMENTAL BIOLOGY; MOUSE; CONSORTIUM; ATLAS; SEGMENTATION; MICROSCOPY; MANAGEMENT; DISCOVERY; FRAMEWORK;
D O I
10.1093/bib/bbw101
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High-throughput phenotyping is a cornerstone of numerous functional genomics projects. In recent years, imaging screens have become increasingly important in understanding gene-phenotype relationships in studies of cells, tissues and whole organisms. Three-dimensional (3D) imaging has risen to prominence in the field of developmental biology for its ability to capture whole embryo morphology and gene expression, as exemplified by the International Mouse Phenotyping Consortium (IMPC). Large volumes of image data are being acquired by multiple institutions around the world that encompass a range of modalities, proprietary software and metadata. To facilitate robust downstream analysis, images and metadata must be standardized to account for these differences. As an open scientific enterprise, making the data readily accessible is essential so that members of biomedical and clinical research communities can study the images for themselves without the need for highly specialized software or technical expertise. In this article, we present a platform of software tools that facilitate the upload, analysis and dissemination of 3D images for the IMPC. Over 750 reconstructions from 80 embryonic lethal and subviable lines have been captured to date, all of which are openly accessible at mousephenotype. org. Although designed for the IMPC, all software is available under an open-source licence for others to use and develop further. Ongoing developments aim to increase throughput and improve the analysis and dissemination of image data. Furthermore, we aim to ensure that images are searchable so that users can locate relevant images associated with genes, phenotypes or human diseases of interest.
引用
收藏
页码:41 / 51
页数:11
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