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Sample GSM7476129 Query DataSets for GSM7476129
Status Public on Jun 20, 2023
Title tail, 0 DPA
Sample type SRA
 
Source name tail
Organism Anolis carolinensis
Characteristics tissue: tail
age: 9-12 months old
time: 0 days post amputation
Extracted molecule total RNA
Extraction protocol Lizard tails were anesthetized by exposing tails to a spray of ethyl chloride for 10 seconds and amputated with a sterile scalpel blade to begin regeneration. Tail samples were collected in Hank’s balanced salt solution (HBSS) supplemented with 100 units/mL penicillin and 100 µg/mL streptomycin (HBSS with P/S). Samples were collected at 0, 1, 3, 7, 14, 21, and 28 days after initial amputation or days post-amputation (DPA) for cell dissociation. Longer tail samples (14, 21 and 28 DPA) were further split into two portions at the original amputation plane using a sterile scalpel. Three tail samples per time point were cut to 3-5 mm pieces in length and each piece was cut into 1/8ths. Tail pieces were added to gentleMACS™ C tubes (Miltenyi Biotec, PN: 130-093-237) containing 2.5 mL Dulbecco’s modified Eagle media (DMEM), 100 µL proprietary Enzyme D, 50 µL Enzyme R and 12.5 µL Enzyme A from Multi Tissue Dissociation Kit 1 (Miltenyi Biotec, PN: 130-110-201). Tubes were inverted and placed onto gentleMACS™ OctoDissociator with sleeve (Miltenyi Biotec, PN: 130-096-427) and a fibroblast dissociation protocol was run for 1 hour. Enzymatic activity was inactivated with DMEM supplemented with 10% fetal bovine serum (FBS). Cells were gently resuspended via pipetting and run through MACS® 70 µm SmartStrainer (Miltenyi Biotec, PN: 130-098-462), followed by filtration via Scienceware FlowMi® 40 µM Cell Strainers for p1000 pipettes (Sigma Aldrich, PN: H13680-0040). Cells were pelleted and washed with DMEM with 10% FBS. Cells were resuspended in HBSS with 0.04% bovine serum albumin (BSA) prior to library preparation.
Isolated cells were counted on a hemocytometer and prepared using the 10x Genomics Chromium Single-Cell Gene Expression kit (V2, PN: 120267) according to manufacturer’s recommendations. Cells were encapsulated into droplets via gel bead-in emulsion (GEM) method for barcoding using the 10x Genomics Chromium controller (PN: 1000202). GEMs were incubated for cDNA synthesis, followed by amplification and library construction, according to manufacturer’s instructions.
 
Library strategy RNA-Seq
Library source transcriptomic single cell
Library selection cDNA
Instrument model Illumina MiSeq
 
Description 10x Genomics
Data processing Demultiplexing, barcode processing, feature counting and aggregation was performed using Cell Ranger pipeline (10x Genomics, v3.1.2)
Assembly: Green anole (A. carolinensis) genome FASTA and GTF files (v2.105) were used to generate a reference genome for indexing by Cell Ranger mkref function (v3.1.2, 10x Genomics). The reference genome FASTA and GTF files were sourced from the Ensembl database for green anole, AnoCar2.0v2 (GCA_000090745.2), ensembl release 105. (http://dec2021.archive.ensembl.org/Anolis_carolinensis/Info/Index).
Supplementary files format and content: Tab-separated values files and matrices
 
Submission date Jun 13, 2023
Last update date Jun 20, 2023
Contact name Thomas P Lozito
E-mail(s) lozito@usc.edu
Organization name University of Southern California
Department Orthopaedic Surgery
Street address 1450 Biggy St NRT4513
City Los Angeles
State/province CA
ZIP/Postal code 90033
Country USA
 
Platform ID GPL23678
Series (1)
GSE234876 Gene expression profile at single-cell level of regenerating lizard (Anolis carolinensis) tail
Relations
BioSample SAMN35726180
SRA SRX20672640

Supplementary file Size Download File type/resource
GSM7476129_D0barcodes.tsv.gz 28.0 Kb (ftp)(http) TSV
GSM7476129_D0features.tsv.gz 177.2 Kb (ftp)(http) TSV
GSM7476129_D0matrix.mtx.gz 9.9 Mb (ftp)(http) MTX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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