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SRX4637902: GSM3374612: lna_cell_mousehuman_resampled; Homo sapiens; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 9.2M spots, 2.8G bases, 1Gb downloads

Submitted by: NCBI (GEO)
Study: Recovery and analysis of transcriptome subsets from pooled single-cell RNA-seq libraries
show Abstracthide Abstract
Single-cell RNA sequencing (scRNA-seq) methods generate sparse gene expression profiles for thousands of single cells in a single experiment. The information in these profiles is sufficient to classify cell types by distinct expression patterns but the high complexity of scRNA-seq libraries prevents full characterization of transcriptomes from individual cells. To generate more focused gene expression information from scRNA-seq libraries, we developed a strategy to physically recover the DNA molecules comprising transcriptome subsets, enabling deeper interrogation of the isolated molecules by another round of DNA sequencing. We applied the method in both a cell-centric and gene-centric mode to isolate mRNA fragments from scRNA-seq libraries. Overall design: targeted resequencing and original untargeted datasets of various scRNA-Seq libraries from the 10x genomics and wafergen platform
Sample: lna_cell_mousehuman_resampled
SAMN09951390 • SRS3736569 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: 10x Illumina libraries at 2nM concentration were diluted 20 fold and PCR amplified with Truseq Pcr F and R oligo for 14 cycles with 1 unit of Phusion. PCR results were confirmed by gel electrophoresis and the remaining sample was Ampure XP purified at a ratio of 1.8x bead/pcr volume. Samples were eluted in 10µl and molarity was determined using a Qubit. 10µl of 100nM library was mixed with 1 µl of 10µM LNA molecule in anneallng buffer (10mM Tris 8.0, 50mM NaCl) and heated to 98˚ for 10 minutes followed by slow cooling to 59˚-64˚ depending on the LNA and held O/N at the annealing temperature. Annealed DNA was added in equal volume to washed Dynabead M270 streptavidin beads at the annealing temperature. Beads were incubated for 15 minutes with gentle shaking. Beads were washed 5x in bind and wash buffer at the annealing temperature. Beads were eluted in 20 µl of elution solution (50mM NaCl, .1mM EDTA) heated for 10 minutes at 100˚ and centrifuged briefly to pellet the streptavidin-bound LNA molecules which inhibit PCR, this elution was done 2 times to ensure all the DNA was removed from the LNA. 10µl of streptavidin purified input DNA was added to PCR using Truseq Pcr F and R for 8 cycles. PCR products were ampure purified, confirmed on the Tapestation D1000, and quantified by the Qubit and submitted for sequencing. Read 1 positions 1-16 contain the 16bp cell barcode, and positions 17-26 contain a 10bp UMI. Read 2 contains the cDNA.
Experiment attributes:
GEO Accession: GSM3374612
Links:
Runs: 1 run, 9.2M spots, 2.8G bases, 1Gb
Run# of Spots# of BasesSizePublished
SRR77828029,200,9802.8G1Gb2018-09-11

ID:
6265288

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