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Sample GSM1506226 Query DataSets for GSM1506226
Status Public on Sep 18, 2014
Title F172 GJ
Sample type SRA
 
Source name stomach_uncultured_bacteria
Organism human gut metagenome
Characteristics host organism: Human
host tissue: stomach
host tissue subsection: gastric juice
biopsy type: gastric juice
helicobacter pylori status: HP positive control
Extracted molecule genomic DNA
Extraction protocol Two pieces of gastric mucosa and gastric juice (500 ul) were excised and subjected to bacterial genomic DNA (gDNA) extraction using a commercial kit (iNtRON Biotechnology, Gyeonggi, Korea). Briefly, the tissues were treated with lysozyme at 37°C for 15 min and lysed with a buffer containing proteinase K and RNase A at 65°C for 15 min. The lysates were subsequently mixed with binding buffer and the gDNA was purified using resin columns.
PCR amplification was performed using primers targeting the V1 to V3 regions of the 16S rRNA gene with extracted DNA. For bacterial amplification, barcoded primer of 9F (5’-CCTATCCCCTGTGTGCCTTGGCAGTC-TCAG-AC-AGAGTTTGATCMTGGCTCAG-3’; underlined sequence indicates the target region primer) and 541R (5’-CCATCTCATCCCTGCGTGTCTCCGAC-TCAG-X-AC-ATTACCGCGGCTGCTGG-3’; ‘X’ indicates the unique barcode for each subject). Pyrosequencing was performed on GS Junior Sequencing system; Chunlab, Inc., Seoul, Korea.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model 454 GS Junior
 
Description Pyrosequencing
Data processing Pyrosequencing analysis was conducted according to the methods described in the previous studies (Hur M, Kim Y, Song HR, et al. Effect of genetically modified poplars on soil microbial communities during the phytoremediation of waste mine tailings. Appl Environ Microbiol 2011;77:7611-9.).
Any reads containing two or more ambiguous nucleotides, reads with low quality score (average score < 25), or reads shorter than 300 base pairs, were discarded. Potential chimeric sequences were detected by the Bellerophon method, which compares the BLASTN search results between the forward half and reverse half sequences.
The taxonomic classification of each read was assigned against the EzTaxon-e database (http://eztaxon-e.ezbiocloud.net), which contains the 16S rRNA gene sequence of type strains that have valid published names and representative species level phylotypes of either cultured or uncultured entries in GenBank public database with complete hierarchical taxonomic classification from the phylum to the species.
The species richness of samples was determined by the abundance-based coverage estimator (ACE), Chao1 estimator and Jackknife estimator. In addition, Simpson diversity index, Shannon diversity index, and Good's library coverage were calculated in the CLcommunity program (Chunlab Inc., Seoul, Korea).
Random subsampling was conducted to equalize the read size of samples for comparing different read sizes among samples. To compare the operational taxonomic units (OTUs) between samples, shared OTUs were obtained with the XOR analysis of the CLcommunity program.
Genome_build: EzTaxon-e database (http://eztaxon-e.ezbiocloud.net)
Supplementary_files_format_and_content: tab-delimited text files include ‘microbial phylotypes classification’ for each sample
 
Submission date Sep 17, 2014
Last update date May 15, 2019
Contact name Jung Min Kim
E-mail(s) jmkim2010@korea.com
Phone 82-10-3459-4776
Organization name NAR Center, Inc. & Genoplan, Inc.
Department Department of Health Genomics
Lab Genetics & Genomics
Street address Gangnam-gu Teheran-ro 216
City Seoul
ZIP/Postal code 06221
Country South Korea
 
Platform ID GPL20020
Series (1)
GSE61493 Analysis of gastric microbiota by pyrosequencing in Korea
Relations
BioSample SAMN03072003
SRA SRX702692

Supplementary file Size Download File type/resource
GSM1506226_F172_GJ.txt.gz 3.9 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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