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Status |
Public on Feb 09, 2020 |
Title |
Single cell RNA-seq of mouse dorsal raphe Pet1 neurons |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Here we use high-throughput and DR subdomain-targeted single-cell transcriptomics and intersectional genetic tools to map molecular and anatomical diversity of DR-Pet1 neurons. We describe up to fourteen neuron subtypes, many showing biased cell body distributions across the DR.
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Overall design |
Single cell RNA-seq libraries prepared from genetically labeled Pet1 neurons in two different ways: (1) automated fluorescence-based cell sorting (using the On-Chip Sort) followed by 10X Genomics Chromium Single Cell 3’ v3 protocol (samples 71-72), or (2) DR subdomain-targeted manual cell sorting, followed by SMART-Seq v4 Ultra Low Input cDNA amplification and Nextera XT library preparation (samples 1-70).
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Contributor(s) |
Okaty BW, Sturrock N |
Citation(s) |
32568072 |
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Submission date |
Feb 08, 2020 |
Last update date |
Jun 29, 2020 |
Contact name |
Benjamin Okaty |
E-mail(s) |
bokaty@genetics.med.harvard.edu
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Organization name |
Harvard Medical School
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Street address |
77 Avenue Louis Pasteur
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
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Platforms (2) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (72)
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Relations |
BioProject |
PRJNA605552 |
SRA |
SRP247768 |