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Sample GSM4766506 Query DataSets for GSM4766506
Status Public on Oct 02, 2020
Title Single cell TCR sequencing of CD4+ Tcells
Sample type SRA
Source name CD4 T Cells
Organism Mus musculus
Characteristics strain: Foxp3eGFP-CreERT2 Rosa26|s|-td-Tomato x Foxp3-GFP
Extracted molecule total RNA
Extraction protocol Single cells were index-sorted using a FACS Aria into 96-well plates containing 5μL of lysis buffer (TCL buffer, Qiagen 1031576) supplemented with 1% β-mercaptoethanol) and frozen in -80°C prior to RT-PCR.
RNA and RT-PCRs for TCRa and TCRb were prepared as previously described (Dash et al., 2011). PCR products for TCRa and TCRb were either subjected to Sanger sequencing or multiplexed with barcodes and submitted to MiSeq sequencing (Han et al., 2014) using True Seq Nano kit (Illumina).
Library strategy OTHER
Library source transcriptomic
Library selection other
Instrument model Illumina MiSeq
Data processing Library strategy: Amplicon-seq
Raw fastq files derived from our RNA-seq libraries were processed with cellranger count (v3.1.0) using the 10x Genomics prebuilt mouse reference (v3.0.0 mm10). Our libraries were processed independently and merged into a single experiment at the analysis level using Seurat (v3.1.1) (Stuart et al., 2019). Quality control was performed by removing cells with high (> 5%) mitochondrial UMI content. Cells having more than 4000 or less than 200 genes were excluded from our analysis. TCR contigs and annotation were performed with the Cellranger vdj workflow from 10x Genomics and the prebuild mouse reference (v3.1.0 mm10). Paired TCR clones were defined by the V, (D), J and CDR3 nucleotide composition for alpha and beta chains. TCR clone sharing was assigned to cells expressing identical V, (D), J, and CDR3 nucleotide and amino acid sequences.  
Raw fastq files were processed by using the mouse transcriptome (gencode M23) with the kallisto (v0.46) software (Bray et al., 2016). Analysis of transcript quantification was performed at the gene level by using the sleuth (v0.30) package for R (Pimentel et al., 2017). Shortly, we modeled batch effect and our experimental design using the sleuth_fit function and detected differentially expressed genes between all groups by the likelihood ratio test (lrt). To spot significantly expressed genes between group pairs, we used the wald-test function. Genes with false discovery rate less than 0.05 and 1 log2 fold-change were used in downstream analysis. Gene set enrichment analysis (GSEA) was performed by using signature gene sets in gmt format and a pre-ranked gene list by log2 fold-change between two groups as input for the fgsea package/R (Korotkevich et al., 2019). Gene ontology (GO) analysis was executed by comparing all detected genes as our background and the lists of differentially expressed genes against the biological processes gene sets by using topGO/R (Alexa and Rahnenfuhrer, 2019; Carlson M, 2019). 
For Miseq data, fastq files were de-multiplexed and paired-end reads were assembled at their overlapping region using PANDASEQ (Masella et al., 2012) and FASTAX toolkit. Demultiplexed and collapsed reads were assigned to wells according to barcodes. Fasta files from both Sanger and Miseq sequences were aligned and analyzed on IMGT ( (Brochet et al., 2008). Cells with identical TCRb CDR3 nucleotide sequences were considered as the same clones. Clonality was confirmed by sequencing TCRa of the expanded clones as assessed by TCRb sequencing for mice shown in Figure S2F and H. Clonality was assigned based on paired TCRab for mice shown in Figure 2 and S2C. Only in frame junction sequences of TCRb were included in the analysis. For fixed-Vb6 mice shown in Figure 2 and S2, each TCRa CDR3 was considered a clone.
Genome_build: mm10
Submission date Sep 03, 2020
Last update date Oct 03, 2020
Contact name Tiago Castro
Organization name The Rockefeller University
Lab Laboratory of Mucosal Immunology
Street address 1230 York Avenue
City New York
State/province New York
ZIP/Postal code 10065
Country USA
Platform ID GPL16417
Series (1)
GSE157453 T cell receptor is required for differentiation but not maintenance of intestinal CD4+ intraepithelial lymphocytes
BioSample SAMN16055582
SRA SRX9072482

Supplementary file Size Download File type/resource
GSM4766506_180110-AB-12p-TCRa.fasta.gz 4.4 Kb (ftp)(http) FASTA
GSM4766506_AB-9p-TCRb.fasta.gz 78.7 Mb (ftp)(http) FASTA
GSM4766506_AB12pTCRb.fasta.gz 136.8 Kb (ftp)(http) FASTA
GSM4766506_TCRa_IMGT.xlsx 410.6 Kb (ftp)(http) XLSX
GSM4766506_TCRb_IMGT.xlsx 746.1 Kb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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