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Status |
Public on Jun 05, 2018 |
Title |
High-Resolution temporal profiling of developing pancreas uncovers the mechanisms of endocrine cell fate determination [Drop-seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
|
Summary |
Drop-sequencing of the whole e14.5 and e16.5 mouse pancreas
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Overall design |
Three litters and 39 mouse embryonic day 14.5 pancreata was dissociated to single cells. 15,228 single cells were sequenced using Drop-seq. For e16.5, three litters and 31 embryos were used and 2,006 transcriptomes were recovered by Drop-seq.
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Contributor(s) |
Hill M, Scavuzzo M, Borowiak M, Martin J |
Citation(s) |
30135482 |
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Submission date |
Jun 28, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Malgorzata Borowiak |
E-mail(s) |
borowiak@bcm.edu
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Organization name |
Baylor College of Medicine
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Street address |
1 Baylor Plaza
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City |
Houston |
ZIP/Postal code |
77030 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (2) |
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This SubSeries is part of SuperSeries: |
GSE100622 |
High-Resolution temporal profiling of developing pancreas uncovers the mechanisms of endocrine cell fate determination |
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Relations |
BioProject |
PRJNA392311 |
SRA |
SRP110702 |