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SRX10498016: viral metagenomic of pig tissuses:Pig93
1 ILLUMINA (Illumina HiSeq 3000) run: 124,774 spots, 62.6M bases, 41.4Mb downloads

Design: For viral metagenomic analysis, 94 different tissues specimens were collected from 94 diseased pigs from Anhui province during Sep 2017 to Sep 2018. The tissue samples of each pig were pooled into the same pool, a total of 94 pools were generated. Those pools were individually homogenized with a mortar and pestle, resuspended in 1 mL DPBS, and then frozen and thawed rapidly three times on dry-ice. The supernatants were then collected after centrifugation (10 min, 15,000 g). Supernatants were filtered through a 0.45-mm filter (Millipore) to remove eukaryotic- and bacterial cell-sized particles, and 200 uL of supernatant from each pool was then subjected to a mixture of nuclease enzymes to reduce the concentration of free (non-viral encapsidated) nucleic acids. Remaining total nucleic acid was then isolated using QIAamp MinElute Virus Spin Kit according to manufacturer's protocol. 94 libraries were then constructed using Nextera XT DNA Sample Preparation Kit (Illumina) and sequenced using the HiSeq Illumina platform with 250 bases paired ends with dual barcoding for each pool.
Submitted by: Jiangsu University
Study: Viral metagenomics of pig tissues
show Abstracthide Abstract
For viral metagenomic analysis, 94 different tissues specimens were collected from 94 diseased pigs from Anhui province during Sep 2017 to Sep 2018. The tissue samples of each pig were pooled into the same pool, a total of 94 pools were generated. Those pools were individually homogenized with a mortar and pestle, resuspended in 1 mL DPBS, and then frozen and thawed rapidly three times on dry-ice. The supernatants were then collected after centrifugation (10 min, 15,000 g). Supernatants were filtered through a 0.45-mm filter (Millipore) to remove eukaryotic- and bacterial cell-sized particles, and 200 uL of supernatant from each pool was then subjected to a mixture of nuclease enzymes to reduce the concentration of free (non-viral encapsidated) nucleic acids. Remaining total nucleic acid was then isolated using QIAamp MinElute Virus Spin Kit according to manufacturer's protocol. 94 libraries were then constructed using Nextera XT DNA Sample Preparation Kit (Illumina) and sequenced using the HiSeq Illumina platform with 250 bases paired ends with dual barcoding for each pool.
Sample:
SAMN18499083 • SRS8600825 • All experiments • All runs
Organism: pig metagenome
Library:
Name: Pig93
Instrument: Illumina HiSeq 3000
Strategy: WGS
Source: METAGENOMIC
Selection: RANDOM PCR
Layout: PAIRED
Runs: 1 run, 124,774 spots, 62.6M bases, 41.4Mb
Run# of Spots# of BasesSizePublished
SRR14127787124,77462.6M41.4Mb2021-04-01

ID:
13931789

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