N.B. The versions of pangolin and nextclade are indicated in the footer of this report. Because of the fast moving nature of the pandemic these versions may not be the most recent, but we check daily for new versions. More details are provided here.

Read Quality control

This section displays basic QC metrics indicating read data quality.

Sequence summaries

Artic Analysis status

The panel below lists samples which failed to produce results from the primary ARTIC analysis. Samples not listed here were analysed successfully, but may still contain inconclusive or invalid results. See the following sections for further indications of failed or inconclusive results.

All samples analysed successfully

Genome coverage

Plots below indicate depth of coverage from data used within the Artic analysis coloured by amplicon pool. Variant filtering during the ARTIC analysis mandates a minimum coverage of at least 20X at variant/genotyping loci for a call to be made.

NB: To better display all possible data, the depth axes of the plots below are not tied between plots for different samples. Care should be taken in comparing depth across samples.

Variant call summaries

The following tables and figures are derived from the output of bcftools stats.

Variant counts:

sample MNPs SNPs indels multiallelic SNP sites multiallelic sites no-ALTs others records
SRR12447502.pass.named.stats 0 7 0 0 0 0 0 7
SRR12480552.pass.named.stats 0 7 0 0 0 0 0 7

Transitions and tranversions:

sample ts tv ts/tv ts (1st ALT) tv (1st ALT) ts/tv (1st ALT)
SRR12447502.pass.named.stats 6 1 6.00 6 1 6.00
SRR12480552.pass.named.stats 6 1 6.00 6 1 6.00

Substitution types

Base substitutions aggregated across all samples (symmetrised by pairing)

Indel lengths

Insertion and deletion lengths aggregated across all samples.

No indels to report.

NextClade analysis

The following view is produced by the nextclade software.

The table shows errors, warnings or failed genes per sample:

index Sample Name clade Failed CDS Warnings Errors
0 SRR12447502 MN908947.3 20C None None None
1 SRR12480552 MN908947.3 20C None None None

Lineage

The table below reports the lineage of each sample as calculated by pangolin.

taxon lineage conflict ambiguity_score scorpio_call scorpio_support scorpio_conflict scorpio_notes version pangolin_version scorpio_version constellation_version is_designated qc_status qc_notes note
SRR12447502 MN908947.3 B.1.319 0.0 NaN NaN NaN NaN NaN PANGO-v1.29 4.3.1 0.3.19 v0.1.12 True pass Ambiguous_content:0.02 Assigned from designation hash.
SRR12480552 MN908947.3 B.1 0.0 NaN NaN NaN NaN NaN PUSHER-v1.29 4.3.1 0.3.19 v0.1.12 False pass Ambiguous_content:0.02 Usher placements: B.1(2/2)

Software versions

The table below highlights versions of key software used within the analysis.

Name Version
nextclade 3.8.2
nextclade_data_tag 2024-02-16T04-00-32Z
pangolin 4.3.1
pangolin-data 1.29
constellations v0.1.12
scorpio 0.3.19
medaka 1.12.1
minimap2 2.18-r1015
bcftools 1.17
samtools 1.18
artic 1.3.0

Workflow parameters

The table below highlights values of the main parameters used in this analysis.

Key Value
out_dir wf-artic
artic_threads 4
pangolin_threads 4
analyse_unclassified False
fastq test_data/fastq
sample None
sample_sheet test_data/sample_sheet.csv
normalise 200
report_depth 100
override_basecaller_cfg None
scheme_name SARS-CoV-2
scheme_version ARTIC/V3
list_schemes False
custom_scheme None
genotype_variants None
report_clade True
report_lineage True
report_coverage True
report_variant_summary True
nextclade_data_tag None
update_data True
lab_id None
testkit None
store_dir wf-artic/store_dir
_min_len 400
_max_len 700
_scheme_version ARTIC/V3
_scheme_name SARS-CoV-2
_max_softclip_length 0
_pangolin_options

About

This report was produced using the epi2me-labs/wf-artic. The workflow can be run using nextflow epi2me-labs/wf-artic --help

Version details Revision: null Git Commit: null

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