E-MTAB-4026 - *Gastrulation* Single-cell RNA sequencing of mouse embryos with Tal1 (Scl) knockout - Bertie Göttgens (Gastrulation_RNA_Seq-sc-3711)

Submitted on 25 March 2015, released on 8 July 2016, last updated on 9 February 2017
Mus musculus
Samples (768)
Protocols (6)
Tracing early mammalian lineage decisions by single cell genomics. Lewis Wolpert famously called gastrulation the most important time in your life. During this fascinating process, a pluripotent stem cell population in the early embryo gives rise to the three germ layers from which all organ systems develop. Cell signalling and transcriptional networks are known to regulate aspects of gastrulation, but the precise mechanisms have not been investigated at the single cell level. Thus, new principles remain to be discovered that govern the exit from naïve pluripotency, epigenetic priming, stochasticity in transcriptional programmes, symmetry breaking, and acquisition of heritable transcriptome patterns. We have brought together a consortium of experts in single cell genomics, mammalian postimplantation development, and computational biology to comprehensively tackle this challenge. We will apply recently established single cell genomics techniques for DNA, RNA, and DNA methylation to profile the majority of the cells in mouse postimplantation embryos. This will result in epigenetic and gene expression maps of most cells together with experimentally determined lineage relationships, hence populating a Waddingtonian landscape. Based on such maps, combinations of transcription factors and epigenetic modifiers will be used to experimentally direct differentiation in human iPS cells.
Experiment types
RNA-seq of coding RNA from single cells, cell type comparison design, genetic modification design
Exp. designProtocolsVariablesProcessedSeq. reads
Investigation descriptionE-MTAB-4026.idf.txt
Sample and data relationshipE-MTAB-4026.sdrf.txt
Additional data (1)E-MTAB-4026.additional.1.zip