Simulated metagenomic DNA sequencing reads for complete NCBI RefSeq virus sequences

This dataset comprises simulated DNA sequencing reads in FASTQ format for 17,900 complete NCBI RefSeq virus sequences downloaded on 2025-02-05. Included are simulated long Oxford Nanopore Technologies R10.4 reads with ~4% error rate and simulated short (2x150bp) Illumina reads with 1% error rate. The source reference sequences are provided as rsviruses17900.fa.gz.

Simulated long reads (Oxford Nanopore Technologies)

rsviruses17900.fastq.gz

Measured empirical error rate: ~4%

Simulator: PBSIM 3.0.4 (https://academic.oup.com/nargab/article/4/4/lqac092/6855700)

Model: ERRHMM-ONT-HQ

Depth: 10x

Mean read length: 1,000bp

Max read length: 10,000bp

Mean accuracy: 0.98

Random seed: 1

Command used:

for fasta in rsviruses17900/*.fa; do    acc=$(basename "$fasta" .fa)   pbsim --seed 1 --strategy wgs --method errhmm --errhmm pbsim3/data/ERRHMM-ONT-HQ.model --depth 10 --genome ${fasta} --prefix ${acc} --id-prefix ${acc}__ --length-mean 1000 --length-max 10000 --accuracy-mean 0.98; cat ${acc}*.fastq | pigz > ${acc}.fastq.gzdone

Simulated short reads (Illumina)

rsviruses17900.r1.fastq.gz and rsviruses17900.r2.fastq.gz

Measured empirical error rate: 1%

Simulator: dwgsim 0.1.14; conda package version 1.1.14, (https://github.com/nh13/DWGSIM)

Read length: 2x150bp (paired)

Depth: 10x

Random read probability (-y): 0

Error rate (-e and -E): 0.01

Mutation rate (-r): 0.0

Of which low frequency somatic mutations (-F): 0.0

Random seed (-z): 1

Command used:

for fasta in rsviruses17900/*.fa; do    acc=$(basename "$fasta" .fa)   dwgsim -C 10 -1 150 -2 150 -y 0.0 -o 1 -z 1 -F 0.0 -r 0.0 -e 0.01 -E 0.01 "$fasta" "$acc"done