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Sample GSM4876111 Query DataSets for GSM4876111
Status Public on Nov 23, 2021
Title tRNA_Seq RNC1
Sample type SRA
 
Source name tRNA_RNC1
Organism Escherichia coli
Characteristics strain: MG1655
Extracted molecule total RNA
Extraction protocol MNase footprinting, ribosome pelleting, RNA extraction, preadenylated linker ligation, rRNA depeletion, reverse transcription, cDNA circularization, PCR amplification (for ribosome profiling) or deacylation reaction, preadenylated linker ligation, rRNA depeletion, reverse transcription, cDNA circularization, PCR amplification (for tRNA-seq)
 
Library strategy ncRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina HiSeq 4000
 
Description tRNA-seq
Data processing Basecalling with Illumina Casava 1.8 software
3' adapter trimming with FastX-toolkit
Library sorting based on sample barcode sequence with custom script
Random barcode triming with custom script
rRNA and other non-coding RNA alignment with bowtie2 v2.1.0
Alignment with bowtie2 v2.1.0
Read quantitation using custom scripts
Genome_build: NC_000913.2
Supplementary_files_format_and_content: text files contain three columns: 1. transcript name;2. CDS region (nt) used for read counting;3. read counts
 
Submission date Nov 02, 2020
Last update date Nov 23, 2021
Contact name tomoya fujita
E-mail(s) tomoya.fujita.at.riken@gmail.com
Organization name RIKEN
Department Cluster for Pioneering Research
Lab RNA Systems Biochemistry Laboratory
Street address 2-1, Hirosawa
City Wako
State/province Saitama
ZIP/Postal code 3510198
Country Japan
 
Platform ID GPL21433
Series (1)
GSE160623 Bacterial ribosome pause sites surveyed by an integration of ribosome profiling and nascent chain profiling
Relations
BioSample SAMN16623552
SRA SRX9417096

Supplementary file Size Download File type/resource
GSM4876111_tRNA_RNC1.txt.gz 490 b (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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