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SRX24123692: Residue microbiotas exposed to natural environment
1 ILLUMINA (Illumina NovaSeq X) run: 63,298 spots, 26.6M bases, 11Mb downloads

Design: The total DNA of all samples (including initial waste materials, residue samples, and larval gut samples) was extracted using the DNeasy PowerSoil Kit (PowerSoil, QIAGEN, Hilden, Germany) according to the manufacturers instructions. Once extracted, the DNA sample was tested by 1% agarose gel electrophoresis. We used the general bacterial primer pair 515F (5-ACTCCTACG GGAGGCAGCAG-3) and 806R (5-GGACTACHVGGGTWTCTAAT-3) to amplify the V4 hypervariable region of the bacterial 16S rRNA gene. PCR was used to amplify the intact DNA samples and then the PCR products were detected by 2% agarose gel electrophoresis. Use the AxyPrep DNA Gel Extraction Kit (AXYGEN Co. Ltd.) to isolate the PCR products. Illumina Novaseq PE250 platform was selected for double-end sequencing with an average of 50,071 raw reads. The raw data of high-through sequencing were available at the NCBI Sequence Read Archive (SRA) database under the accession.
Submitted by: Zhejiang University
Study: Residue and larval gut microbiotas during BSFL bioconversion under two strategies
show Abstracthide Abstract
This study combined a laboratory-scale experiment and a case study to explore the BSFL bioconversion of agri-food waste (chicken manure and food waste) generated in Gaoqiao Subdistrict, China under the independent and co-treatment strategies.
Sample: not provided
SAMN40650000 • SRS20909221 • All experiments • All runs
Organism: gut metagenome
Library:
Name: CG10_r3
Instrument: Illumina NovaSeq X
Strategy: AMPLICON
Source: GENOMIC
Selection: PCR
Layout: SINGLE
Runs: 1 run, 63,298 spots, 26.6M bases, 11Mb
Run# of Spots# of BasesSizePublished
SRR2852278163,29826.6M11Mb2024-04-06

ID:
32434194

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