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Sample GSM4700366 Query DataSets for GSM4700366
Status Public on Apr 15, 2021
Title E11-C-10A
Sample type SRA
 
Source name embryo cell
Organism Macaca fascicularis
Characteristics tissue: embryo
development stage: E11
lineage: EPI
Extracted molecule total RNA
Extraction protocol The single-cell was washed in 30µL micro-drop of PBS-BSA solution and individual cells were picked into 0.2mL PCR tubes by micropipette for modified Smart2-seq,all the cDNA were quantified on a 2100 Bioanalyzer (Agilent) and Qubit 3.0.
The scRNA-seq libraries were generated using the TruePrepTM DNA Library Prep Kit V2 for Illumina®(Vazyme) . Briefly, we use 5-50ng cDNA constructing the libraries according to the manufacturer’s instructions. cDNA molecules were preamplified and pooled followed by library construction. All libraries were quantified on a 2100 Bioanalyzer (Agilent) and realtime quantitative PCR, and then subjected to 150 bp paired-end sequencing on an Illumina Xten platform (sequenced by Novogene and Annoroad).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Description Chimera embryo cell of Macaca fascicularis
Data processing fastp was used to cut adapters and quality control
human and monkey cells were identified by two ways using the clean data. One way is to compare the number of identical hits of sequencing reads from each cell by blastp with the random selected 10000 reads against the human and monkey genome (Ensembl Homo_sapiens.GRCh38 and Macaca_fascicularis_5.0), respectively. Another way is to compare the reads counts of sequencing reads mapped to tdTomato vector.
hisat2 was used to map sequencing reads to the human or monkey genome with the default parameters.
The program stringtie with default parameters was used to assembly alignments into potential transcripts
Quantify the gene expression as transcripts per million mapped reads (TPM) value by the program stringtie
Genome_build: Homo_sapiens.GRCh38 and Macaca_fascicularis_5.0
Supplementary_files_format_and_content: tab-delimited text file include TPM matrix for all samples
 
Submission date Jul 29, 2020
Last update date Apr 15, 2021
Contact name shaoxing Dai
E-mail(s) daishx08@gmail.com
Phone 15287145159
Organization name Kunming University of Science and Technology
Street address No.1 boda road chenggong, Kunming 650500 Yunnan,China
City 昆明市
State/province 云南
ZIP/Postal code 650500
Country China
 
Platform ID GPL28212
Series (1)
GSE155381 Chimeric contribution of human extended pluripotent stem cells to monkey embryos
Relations
BioSample SAMN15671356
SRA SRX8846200

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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