{% extends "base.html" %} {% block content %}
Sequences: {{ summary.sequences }}
Alignment length: {{ summary.alignment_length }}
Mean N content: {{ summary.mean_n_content }}
Mean completeness: {{ summary.mean_completeness }}
Purple blocks represent N positions (ambiguous nucleotides) along the alignment for each sequence.
{% if n_blocks_plot_note %}
{{ n_blocks_plot_note }}
{% endif %}
No alignment data available for plotting.
{% endif %}Categories of mutations checked were {{ flagged_criteria }}.
{% if sites_table %}| {{ header }} | {% endfor %}
|---|
| {{ cell }} | {% endfor %}
No sites flagged for review.
{% endif %}Categories of mutations checked were {{ flagged_criteria }}.
{% if flagged_plot_html %} {{ flagged_plot_html | safe }} {% else %}No sites flagged for review.
{% endif %}Sequences are flagged for removal if they meet the following criteria: {{ flagged_removal_criteria }}.
{% if sequence_removals_table %}| {{ header }} | {% endfor %}
|---|
| {{ cell }} | {% endfor %}
No sequences flagged for removal.
{% endif %}This plot shows sequence diversity across the alignment as Shannon diversity, smoothed over a {{ smoothing_window }}-base window.
Shannon diversity summarizes how mixed the bases are at each alignment position: low values mean most sequences share the same base,
and higher values mean more diversity at a given position. For a column with possible states A/T/C/G (Ns and gaps are ignored), the theoretical range is 0 to log₂(4) ≈ 2.0.
High diversity can be a sign of true biological variation, but it can also indicate problematic sites with many sequencing errors or misalignments.
No diversity plot available.
{% endif %}