|
Status |
Public on May 25, 2020 |
Title |
Bulk Exponential Wild-Type E. coli |
Sample type |
SRA |
|
|
Source name |
Liquid Culture
|
Organism |
Escherichia coli |
Characteristics |
library prep: Bulk growth stage: Exponential fixed: Yes
|
Growth protocol |
Cells were diluted 1:100 or 1:50 into fresh media from an overnight culture and grown 2 hours (exponential) or 5 hours (stationary)
|
Extracted molecule |
total RNA |
Extraction protocol |
PETRI-seq libraries were subjected to in situ RT and ligations followed by cell lysis with detergent and proteinase K; Bulk libraries were prepared from fixed cells after lysis with detergent and proteinase K Double-stranded cDNA was made by second strand synthesis. Libraries were tagmented and amplified using the Nextera XT kit
|
|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
cDNA prepared from the same cells as SB442 SB432_SB433_FC
|
Data processing |
Barcode demultiplexing with cutadapt 1.18 UMIs extracted with UMI-tools version 0.5.5 Reads aligned with bwa version 0.7.17 Features called with featureCounts version 1.6.3 Final matrix generated by collapsing reads by UMI with a custom script in python 2.7.15 Genome_build: Genbank U00096; Genbank CP000255.1 Supplementary_files_format_and_content: tab-delimited txt
|
|
|
Submission date |
Apr 21, 2020 |
Last update date |
May 25, 2020 |
Contact name |
Sydney B Blattman |
E-mail(s) |
sb3292@columbia.edu
|
Organization name |
Columbia University
|
Lab |
Tavazoie Lab
|
Street address |
1150 St. Nicholas Ave
|
City |
New York |
State/province |
NY |
ZIP/Postal code |
10032 |
Country |
USA |
|
|
Platform ID |
GPL21222 |
Series (1) |
GSE141018 |
Prokaryotic Single-Cell RNA Sequencing by In Situ Combinatorial Indexing |
|
Relations |
BioSample |
SAMN14655909 |
SRA |
SRX8151655 |