4.7 Article

Combination of novel and public RNA-seq datasets to generate an mRNA expression atlas for the domestic chicken

Journal

BMC GENOMICS
Volume 19, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12864-018-4972-7

Keywords

Chicken; Gallus gallus; Expression atlas; RNA-seq; Network graph

Funding

  1. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/M011925/1]
  2. institute strategic program grant 'Farm Animal Genomics' [BBS/E/D/20211550]
  3. institute strategic program grant 'Transcriptomes, Networks and Systems' [BBS/E/D/20211552]
  4. Rural and Environmental Science and Analytical Sciences Division of the Scottish Government
  5. BBSRC LINK project
  6. Aviagen Ltd. [BB/J006815/1]
  7. BBSRC [BB/J004243/1]
  8. Natural Environmental Research Council [R8/H10/56]
  9. Medical Research Council [MR/K001744/1]
  10. BBSRC [BB/J006815/1, BBS/E/D/20320000, BBS/E/D/20211552, BBS/E/D/20310000, BBS/E/D/20211550, BB/M011925/1] Funding Source: UKRI
  11. MRC [MR/K001744/1] Funding Source: UKRI

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Background: The domestic chicken (Gallus gallus) is widely used as a model in developmental biology and is also an important livestock species. We describe a novel approach to data integration to generate an mRNA expression atlas for the chicken spanning major tissue types and developmental stages, using a diverse range of publicly-archived RNA-seq datasets and new data derived from immune cells and tissues. Results: Randomly down-sampling RNA-seq datasets to a common depth and quantifying expression against a reference transcriptome using the mRNA quantitation tool Kallisto ensured that disparate datasets explored comparable transcriptomic space. The network analysis tool Graphia was used to extract clusters of co-expressed genes from the resulting expression atlas, many of which were tissue or cell-type restricted, contained transcription factors that have previously been implicated in their regulation, or were otherwise associated with biological processes, such as the cell cycle. The atlas provides a resource for the functional annotation of genes that currently have only a locus ID. We cross-referenced the RNA-seq atlas to a publicly available embryonic Cap Analysis of Gene Expression (CAGE) dataset to infer the developmental time course of organ systems, and to identify a signature of the expansion of tissue macrophage populations during development. Conclusion: Expression profiles obtained from public RNA-seq datasets-despite being generated by different laboratories using different methodologies - can be made comparable to each other. This meta-analytic approach to RNA-seq can be extended with new datasets from novel tissues, and is applicable to any species.

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