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pmid:27275414

Combined sequencing of mRNA and DNA from human embryonic stem cells.

Florian Mertes · Heiner Kuhl · Wasco Wruck · Hans Lehrach · James Adjaye

Genomics data · 2016 doi:10.1016/j.gdata.2016.04.014

Paper

complete

Experiment

complete

Data

partial

Analysis

absent

Execution

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title
Combined sequencing of mRNA and DNA from human embryonic stem cells.
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10.1016/j.gdata.2016.04.014
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Florian Mertes
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Heiner Kuhl
[2]
Wasco Wruck
[3]
Hans Lehrach
[4]
James Adjaye
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Genomics data
year
2016
abstract
Combined transcriptome and whole genome sequencing of the same ultra-low input sample down to single cells is a rapidly evolving approach for the analysis of rare cells. Besides stem cells, rare cells originating from tissues like tumor or biopsies, circulating tumor cells and cells from early embryonic development are under investigation. Herein we describe a universal method applicable for the analysis of minute amounts of sample material (150 to 200 cells) derived from sub-colony structures from human embryonic stem cells. The protocol comprises the combined isolation and separate amplification of poly(A) mRNA and whole genome DNA followed by next generation sequencing. Here we present a detailed description of the method developed and an overview of the results obtained for RNA and whole genome sequencing of human embryonic stem cells, sequencing data is available in the Gene Expression Omnibus (GEO) database under accession number GSE69471.
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Combined ultra-low input mRNA and whole-genome sequencing from human embryonic stem cells
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