NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4322679 Query DataSets for GSM4322679
Status Public on Apr 17, 2020
Title single cell from LSK-SLAM-13.22 [LIB021528_GEN00057132_S77_R1]
Sample type SRA
 
Source name Fetal liver (FL)
Organism Mus musculus
Characteristics tissue: embryonic tissue
strain: C57BL/6
Extracted molecule total RNA
Extraction protocol Embryos were harvested from the uterus and dissected in cold dissecting buffer (Dulbecco’s phosphate buffered saline with 10% fetal bovine serum and antibiotics). Dissected tissues were dissociated in 0.125% collagenase type I (Sigma-Aldrich) and 1 U Dispase (Stemcell Technologies) at 37°C for 30 min. The samples were reduced to single cell suspension by mechanical trituration, washed with dissecting media, and passed through 40mm cell strainer. FACS was used to enrich single cell population of interest
Cells were lysed and single cell libraries prepared by the C1 System using the SMARTer Ultra Low RNA Kit (Clontech) and protocols provided by Fluidigm.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description LIB021528_GEN00057132_S77_R1
Data processing We only use R1 from the pair-end sequence reads. Sequence reads were trimmed to a final length of 40 bases using Trimming software Cutadapt (Martin, 2011).
Salmon (Patro et al., 2017) was used to quasi-map trimmed reads to the reference transcriptome (ENSEMBL (Zerbino et al., 2018) GRCh38.80), including 6511 non-coding RNAs (scaRNAs, lincRNAs, snRNAs, and snoRNAs), to estimate transcript abundances. The number of reads mapping to the transcriptome ranged from 7.7 to 12.0 million. Read counts per gene were derived by summing the counts per transcript across all transcripts associated with the gene
For quality control measures, 0.1% of reads were randomly sampled from each FASTQ and directly aligned to ENSEMBL GRC Release 80 (ftp://ftp.ensembl.org/pub/release-80/gtf/) reference genomes using HISAT2 (Kim et al., 2015) to determine percentage alignment to H. Sapiens, M. Musculus, S. Cerevisiae, E. Coli, and D. Rerio genomes, as well as overlaps with genomic features (including rRNA, mtRNA, protein-coding regions), ambiguous and non-unique alignments, and unaligned reads.
Genome_build: GRCm38
Supplementary_files_format_and_content: comma delimited files containing metadata and count matrix for all samples
 
Submission date Feb 20, 2020
Last update date Apr 17, 2020
Contact name Yuqi Tan
Organization name Johns Hopkins University
Street address 733 North Broadway, MRB 653
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL17021
Series (1)
GSE145638 Transcriptome dynamics of hematopoietic stem cell formation revealed using a combinatorial Runx1/Ly6a reporter system
Relations
BioSample SAMN14146380
SRA SRX7760507

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

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap