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Sample GSM7018754 Query DataSets for GSM7018754
Status Public on Jun 07, 2023
Title SCHW00051
Sample type SRA
 
Source name brain
Organism Mus musculus
Characteristics tissue: brain
cell type: Dbh-Cre; Ai14 Neuron
Extracted molecule total RNA
Extraction protocol Fresh brain tissue was placed in ice-cold aCSF (2.5 mM KCl, 7 mM MgCl2, 0.5 mM CaCl2, 1.3 mM NaH2PO4, 110 mM choline chloride, 25 mM NaHCO3, 1.3 mM sodium ascorbate, 20 mM glucose, 0.6 mM sodium pyruvate, bubbled in 95% O2 /5%CO2). 200 μm coronal slices that included the LC were collected. Slices were transferred to a 32°C holding chamber containing oxygenated aCSF, where they recovered for at least 1 hour. tdTomato-expressing LC neurons were manually extracted from the slice using glass pipettes pulled from borosilicate glass (World Precision Instruments) to create an ~50 µm tip. The ends of glass pipette tips containing picked cells were snapped into individual wells of a 96 well plate containing 4µl lysis buffer: 0.1µl RNase inhibitor (Thermo Scientific), 0.1µl ERCC RNA spike-in (Invitrogen), 0.02µl 10% Triton (Sigma), 1µl 10mM dNTP (Invitrogen), 0.1µl 100µM dT (IDT; 5'-AAGCAGTGGTATCAACGCAGAGTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTVN), and 2.68µl H2O.
Samples underwent primer annealing (72℃ for 3min) before placing on ice. Next, 6µl reverse transcription reagent was added to each sample: 0.14µl H2O, 0.25µl RNase inhibitor, 2µl 5X First Strand Buffer (Clontech), 0.5µl 100mM DTT (Invitrogen), 2µl 5M Betaine (Sigma), 0.06µl 1M MgCl2 (Invitrogen), 0.1µl 100µM TSO (Qiagen; 5'-AAGCAGTGGTATCAACGCAGAGTACATrGrG+G), 0.95µl SmartScribe enzyme (Clontech). Samples were incubated at 42℃ for 90min, 70℃ for 5min, then held at 4℃. DNA preamplification solution (15µl) was next added to each sample: 2.1375µl H2O, 12.5µl 2X Kapa HiFi Hot Start Ready Mix (Kapa Biosystems), 0.25µl 10µM IS_PCR Primer (IDT; 5'-AAGCAGTGGTATCAACGCAGAGT), 0.1125µl Lambda Exonuclease (NEB). Samples were incubated at 37℃ for 30min, 95℃ for 3min, 21 cycles of [98℃ for 20s, 67℃ for 15sec, 72℃ for 4min], 72℃ for 5min, and then held at 4℃. DNA cleanup, quantification, dilution, tagmentation, and barcoding were performed by the Hartwell Center at St. Jude Children’s Research Hospital using standard methods.
Smart-seq2
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Sequences were de-multiplexed using bcl2fastq and aligned to mouse mm10 genome (with Cre and tdTomato genes added).
Paired-end reads from Illumina were trimmed for adapters by cutadapt(v1.15) and aligned to mm9 (MGSCv37, NCBI) by STAR(v2.5.2b, parameters "--outFilterType BySJout --outFilterMultimapNmax 20 --alignSJoverhangMin 8 --alignSJDBoverhangMin 1 --outFilterMismatchNmax 999 --alignIntronMin 20 --alignIntronMax 1000000 --alignMatesGapMax 1000000 --outFileNamePrefix SCHW00296. --outSAMstrandField intronMotif --genomeLoad NoSharedMemory --outSAMattributes NH HI NM MD AS nM XS --outSAMunmapped Within KeepPairs --outSAMtype BAM SortedByCoordinate --twopassMode Basic --outFilterScoreMinOverLread 0.33 --outFilterMatchNminOverLread 0.33 --outReadsUnmapped Fastx").
LiftOver was performed on GENCODE(vM9) gene database (from mm10 to mm9) by CrossMap(v0.1.5) to improve gene annotation.
Aligned reads were then counted by HTSEQ (v 0.6.1p1) for genes annotated in GENCODE database. Trimmed reads were also run through FastQ Screen(v0.9.5) against Human, Mouse, Adapters, Univec databases (Dec 2016) to check for contamination and doublets. Samples with larger unique hits to human over mouse genomes were considered putative doublets and excluded from analysis. We further excluded samples with less than 1M reads and those that did not express Dbh.
Assembly: mm9
Supplementary files format and content: raw counts table and quality control matrix
 
Submission date Feb 01, 2023
Last update date Jun 07, 2023
Contact name Beisi Xu
E-mail(s) beisi.xu@stjude.org
Organization name St Jude Children's Research Hosipital
Department Center for Applied Bioinformatics
Street address 262 Danny Thomas Pl
City Memphis
State/province Tennessee
ZIP/Postal code 38105
Country USA
 
Platform ID GPL24247
Series (1)
GSE224285 A Novel Single Vector Intersectional AAV Strategy for Interrogating Cellular Diversity and Brain Function
Relations
BioSample SAMN33010007
SRA SRX19250164

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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