nextclade
Bioinformatics tool for virus genome alignment, clade assignment, and qc checks. tldr-pages
On several platforms
Several platforms
Align sequences to user provided reference, outputting the alignment to a file
nextclade run path/to/sequences.fa --input-ref path/to/reference.fa --output-fasta path/to/alignment.faIdentifyCreate a TSV report, auto-downloading the latest dataset
nextclade run path/to/fasta --dataset-name dataset_name --output-tsv path/to/report.tsvIdentifyList all available datasets
nextclade dataset listIdentifyDownload the latest SARS-CoV-2 dataset
nextclade dataset get --name sars-cov-2 --output-dir path/to/directoryIdentifyUse a downloaded dataset, producing all outputs
nextclade run --input-dataset path/to/dataset_directory --output-all path/to/output_directory path/to/sequences.fastaIdentifyRun on multiple files
nextclade run --dataset-name dataset_name --output-tsv path/to/output_tsv -- path/to/input_fasta_1 path/to/input_fasta_2 ...IdentifyTry reverse complement if sequence does not align
nextclade run --retry-reverse-complement --dataset-name dataset_name --output-tsv path/to/output_tsv path/to/input_fastaIdentify