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command line invocation , main output files (consensus, VCF, json)
New features that people are likely to care about:
Coverage on SNP (not indel) alleles reported in VCF
A new summary block added to the output JSON which should include everything anyone needs to look at results and QC (separating this from internal/debug output in the JSON). Intention is users should generally only need to look here.
Output JSON records state of how far through the process the workflow has gone.
Subtle changes in quality of assembly sequence
Slightly fewer Ns called in primers due to improved primer-aware QC
Consensus will include the very first and last primers in the genome
Lengths of runs of Ns now fixed to match the length of associated sequence in the reference (ie not intended to imply indels)
Improved robustness
Additional robustness against pathological cases with ARTIC4.1 (which we have not actually ever seen in real life)
Performance/speed
High depth samples are subsampled to 1000x (per amplicon) thus controlling runtime and RAM. Will control runtime for the crazy-big samples in the ENA .
New debug output
new TSV file produced which shows coverage of different bases at each position
Internal changes
Large amount of code refactoring
Test process
Unit tests improved
Tests on simulated genomes with specific error-modes in primers
Tests on nanopore/illumina ARTIC/midnight truth samples using covid-truth-eval framework
Robustness check running on tens of thousands of genomes from ENA.
The text was updated successfully, but these errors were encountered:
Unchanged
New features that people are likely to care about:
Subtle changes in quality of assembly sequence
Improved robustness
Performance/speed
New debug output
Internal changes
Test process
The text was updated successfully, but these errors were encountered: