U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX15678236: WGS of African Swine Fever Virus: Dominican Republic Swine (Nanopore)
1 OXFORD_NANOPORE (GridION) run: 274,084 spots, 1.2G bases, 1Gb downloads

Design: The best reference from the NCBI RefSeq database was determined by aligning reads against all references and selecting the reference genome with the closest identity and breadth of coverage. The closest reference genome by identity was Georgia 2007/1 (NC_044959.2). Reference-guided alignment was performed using BWA-MEM (0.7.17-r1188) for Illumina data and Minimap2 (version 2.21-r1071) for Oxford Nanopore data. Variant calling against the Georgia 2007/1 reference was performed using Freebayes (version 1.3.4) against the population of samples. Variants were filtered based on quality score, depth, and log-odds ratio to remove low-confidence variants. This produced a sample set with 21 total variant sites, all of which were single nucleotide polymorphisms. These variants were applied to the Georgia 2007/1 genome to produce the final consensuses. Annotations were transferred from the Georgia 2007/1 genome, and changes in gene coding sequences were modified accordingly. The samples in this BioProject include raw data files and genome consensus sequences against Georgia 2007/1 based on reference-guided assembly.
Submitted by: USDA/APHIS/FADDL
Study: Genome Sequences and Sequence Data of African Swine Fever virus from the Dominican Republic 2021
show Abstracthide Abstract
Diagnostic samples from swine were provided to the USDA Foreign Animal Disease Diagnostic Laboratory (FADDL) for testing originating from the Dominican Republic. Initial tests indicated the presence of African Swine Fever virus, which was subsequently submitted for whole genome sequencing for confirmation and characterization. Samples were provided as blood and tissue obtained from affected swine in May through early August 2021. Samples were sequenced on the Oxford Nanopore PromethION and the Illumina MiSeq platforms. The best reference from the NCBI RefSeq database was determined by aligning reads against all references and selecting the reference genome with the closest identity and breadth of coverage. The closest reference genome by identity was Georgia 2007/1 (NC_044959.2). Reference-guided alignment was performed using BWA-MEM (0.7.17-r1188) for Illumina data and Minimap2 (version 2.21-r1071) for Oxford Nanopore data. Variant calling against the Georgia 2007/1 reference was performed using Freebayes (version 1.3.4) against the population of samples. Variants were filtered based on quality score, depth, and log-odds ratio to remove low-confidence variants. This produced a sample set with 21 total variant sites, all of which were single nucleotide polymorphisms. These variants were applied to the Georgia 2007/1 genome to produce the final consensuses. Annotations were transferred from the Georgia 2007/1 genome, and changes in gene coding sequences were modified accordingly. The BioSamples in this BioProject include raw data files and genome consensus sequences against Georgia 2007/1 based on reference-guided assembly. These genomes have not been finished and may contain additional structural variations that were not detected by the sequencing performed here.
Sample: 9903495
SAMN28980129 • SRS13376255 • All experiments • All runs
Library:
Name: ASFV_DR2021_065_nanopore
Instrument: GridION
Strategy: WGS
Source: METAGENOMIC
Selection: other
Layout: SINGLE
Runs: 1 run, 274,084 spots, 1.2G bases, 1Gb
Run# of Spots# of BasesSizePublished
SRR19627684274,0841.2G1Gb2022-07-29

ID:
22303212

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...