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<h1 id="select-column-projection-and-aggregation"><code>select</code> — column projection and aggregation</h1>
<p><code>select</code> transforms an index by operating on its <strong>genome columns</strong>: projecting a
subset of columns, aggregating groups of genomes into synthetic columns, or both.
It is the column-axis counterpart of <code>filter</code> (row-axis operations).</p>
<p>Following relational algebra conventions:</p>
<table>
<thead>
<tr>
<th>Command</th>
<th>Relational operation</th>
<th>Axis</th>
</tr>
</thead>
<tbody>
<tr>
<td><code>filter</code></td>
<td>σ — selection</td>
<td>rows (k-mers)</td>
</tr>
<tr>
<td><code>select</code></td>
<td>π — projection</td>
<td>columns (genomes)</td>
</tr>
</tbody>
</table>
<p>The two commands compose naturally: run <code>filter</code> first to restrict the kmer set,
then <code>select</code> to reshape the genome columns.</p>
<p><code>select</code> never changes the kmer set. The MPHF and <code>unitigs.bin</code> of each layer
are preserved unchanged; only the data matrices are rewritten.</p>
<hr />
<h2 id="synopsis">Synopsis</h2>
<div class="highlight"><pre><span></span><code>obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>&lt;input-index&gt;
<span class="w"> </span>--output<span class="w"> </span>&lt;dir&gt;
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<span class="w"> </span><span class="o">[</span>--group<span class="w"> </span>&lt;name&gt;:&lt;pred&gt;<span class="w"> </span>...<span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--group-op<span class="w"> </span>&lt;name&gt;:&lt;op&gt;<span class="w"> </span>...<span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--aggregate-by<span class="w"> </span>&lt;key&gt;<span class="w"> </span><span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--aggregate-op<span class="w"> </span>&lt;op&gt;<span class="w"> </span><span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--select<span class="w"> </span>&lt;col1,col2,...&gt;<span class="w"> </span><span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--presence-threshold<span class="w"> </span>&lt;N&gt;<span class="w"> </span><span class="o">]</span>
<span class="w"> </span><span class="o">[</span>--force-copy<span class="w"> </span><span class="o">]</span>
2026-08-15 20:56:29 +02:00
</code></pre></div>
<hr />
<h2 id="output-destination">Output destination</h2>
<p><code>--output &lt;dir&gt;</code> is required — <code>select</code> always writes a new index; there is no
<code>--in-place</code> mode (2026-08-28: never implemented, removed from the design). The
source index is unchanged.</p>
<p>Each layer's kmer-identity files (<code>mphf.bin</code>/<code>unitigs.bin</code>/<code>evidence.bin</code>/
<code>unitigs.bin.idx</code>/<code>fingerprint.bin</code>/<code>layer_meta.json</code>) are never rewritten by a
column projection/aggregation, so they are hard-linked into the output rather
than copied — no extra disk for them even on a large index. Falls back to a
real copy automatically if linking fails (different filesystems); <code>--force-copy</code>
forces a real copy always, for an output that must survive independently of the
source on disk (a hard link shares the same inode — rewriting one path outside
<code>select</code> itself would affect the other). Only the <code>presence</code>/<code>counts</code>
subdirectory is ever a genuinely new, independent file.</p>
<p>To replace an index with a selected version of itself, select to a temporary
directory and swap it in (<code>rm -rf INDEX &amp;&amp; mv INDEX.tmp INDEX</code>) — the case
<code>--in-place</code> used to cover.</p>
2026-08-15 20:56:29 +02:00
<hr />
<h2 id="defining-output-columns">Defining output columns</h2>
<h3 id="named-groups-group">Named groups — <code>--group</code></h3>
<div class="highlight"><pre><span></span><code>--group &lt;name&gt;:&lt;pred&gt;
</code></pre></div>
<p>Defines a named group of genomes using the same predicate syntax as <code>filter</code>.
Repeatable; a genome can belong to several groups.</p>
<div class="highlight"><pre><span></span><code>--group<span class="w"> </span><span class="s2">&quot;pub:species=Betula_pubescens&quot;</span>
--group<span class="w"> </span><span class="s2">&quot;nan:species=Betula_nana&quot;</span>
</code></pre></div>
<h3 id="per-group-operator-group-op">Per-group operator — <code>--group-op</code></h3>
<div class="highlight"><pre><span></span><code>--group-op &lt;name&gt;:&lt;op&gt;
</code></pre></div>
<p>Assigns an aggregation operator to a named group. Optional; if absent, the
default operator applies (see below).</p>
<div class="highlight"><pre><span></span><code>--group-op<span class="w"> </span><span class="s2">&quot;pub:any&quot;</span>
--group-op<span class="w"> </span><span class="s2">&quot;nan:all&quot;</span>
</code></pre></div>
<h3 id="shorthand-aggregate-by-aggregate-op">Shorthand — <code>--aggregate-by</code> / <code>--aggregate-op</code></h3>
<p><code>--aggregate-by &lt;key&gt;</code> automatically creates one group per unique value of the
metadata key <code>&lt;key&gt;</code>. Equivalent to one <code>--group &lt;val&gt;:&lt;key&gt;=&lt;val&gt;</code> per distinct
value. <code>--aggregate-op &lt;op&gt;</code> sets the operator for all auto-generated groups.</p>
<p><code>--aggregate-by</code> and <code>--group</code> are mutually exclusive.</p>
<h3 id="column-selection-and-ordering-select">Column selection and ordering — <code>--select</code></h3>
<div class="highlight"><pre><span></span><code>--select col1,col2,...
</code></pre></div>
<p>Lists the output columns in order. Each element is either a group name (defined
by <code>--group</code> or generated by <code>--aggregate-by</code>) or a genome label from the source
index (pass-through, no aggregation).</p>
<p><strong>Default when <code>--select</code> is absent:</strong>
all defined groups in declaration order (for <code>--group</code>), or all generated groups
in metadata-value order (for <code>--aggregate-by</code>). Individual genomes not in any
group are excluded unless named explicitly.</p>
<p><strong>When neither <code>--group</code> nor <code>--aggregate-by</code> is specified:</strong>
<code>--select</code> can still reference genome labels for pure column projection (no
aggregation). If <code>--select</code> is also absent, all genomes are output unchanged
(identity transform — useful combined with row filtering via a prior <code>filter</code>
run).</p>
<hr />
<h2 id="aggregation-operators">Aggregation operators</h2>
<table>
<thead>
<tr>
<th>Operator</th>
<th>Input</th>
<th>Output</th>
<th>Semantics</th>
</tr>
</thead>
<tbody>
<tr>
<td><code>any</code></td>
<td>pres / count</td>
<td>presence</td>
<td>1 if ≥ 1 genome in group carries the k-mer</td>
</tr>
<tr>
<td><code>all</code></td>
<td>pres / count</td>
<td>presence</td>
<td>1 if every genome in group carries the k-mer</td>
</tr>
<tr>
<td><code>none</code></td>
<td>pres / count</td>
<td>presence</td>
<td>1 if no genome in group carries the k-mer</td>
</tr>
<tr>
<td><code>sum</code></td>
<td>count</td>
<td>count</td>
<td>sum of counts across the group</td>
</tr>
<tr>
<td><code>min</code></td>
<td>count</td>
<td>count</td>
<td>minimum count</td>
</tr>
<tr>
<td><code>max</code></td>
<td>count</td>
<td>count</td>
<td>maximum count</td>
</tr>
</tbody>
</table>
<p><strong>Default operator:</strong>
- Presence index: <code>any</code>
- Count index: <code>sum</code></p>
<p>Logical operators (<code>any</code>/<code>all</code>/<code>none</code>) on a count index use
<code>--presence-threshold N</code> (default 0): a genome "carries" the k-mer if its count
is &gt; N.</p>
<p><strong>Output index type:</strong>
- If the source is a presence index, the output is always a presence index.
- If the source is a count index and every output column uses a logical operator
or is a pass-through from a presence source, the output is a presence index.
- Otherwise (at least one arithmetic operator on a count source), the output is
a count index.</p>
<hr />
<h2 id="behaviour-for-edge-cases">Behaviour for edge cases</h2>
<table>
<thead>
<tr>
<th>Situation</th>
<th>Behaviour</th>
</tr>
</thead>
<tbody>
<tr>
<td>Genome missing the metadata key in <code>--aggregate-by</code></td>
<td>genome ignored (no <code>NA</code> group)</td>
</tr>
<tr>
<td>Genome in multiple groups</td>
<td>contributes independently to each</td>
</tr>
<tr>
<td><code>--group-op</code> references undefined group</td>
<td>error</td>
</tr>
<tr>
<td><code>--select</code> element is neither group name nor genome label</td>
<td>error</td>
</tr>
<tr>
<td><code>--output</code> and <code>--in-place</code> both specified</td>
<td>error</td>
</tr>
<tr>
<td>Neither <code>--output</code> nor <code>--in-place</code></td>
<td>error</td>
</tr>
<tr>
<td>Group with zero matching genomes</td>
<td>column is all-zeros (or all-ones for <code>none</code>)</td>
</tr>
</tbody>
</table>
<hr />
<h2 id="examples">Examples</h2>
<h3 id="aggregate-by-metadata-group-default-operators">Aggregate by metadata group, default operators</h3>
<div class="highlight"><pre><span></span><code>obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>myindex<span class="w"> </span>--output<span class="w"> </span>out<span class="w"> </span>--aggregate-by<span class="w"> </span>group
<span class="c1"># one column per unique value of &quot;group&quot;; presence→any, count→sum</span>
</code></pre></div>
<h3 id="named-groups-with-different-operators">Named groups with different operators</h3>
<div class="highlight"><pre><span></span><code>obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>myindex<span class="w"> </span>--output<span class="w"> </span>out<span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--group<span class="w"> </span><span class="s2">&quot;pub:species=Betula_pubescens&quot;</span><span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--group<span class="w"> </span><span class="s2">&quot;nan:species=Betula_nana&quot;</span><span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--group-op<span class="w"> </span><span class="s2">&quot;pub:any&quot;</span><span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--group-op<span class="w"> </span><span class="s2">&quot;nan:all&quot;</span><span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--select<span class="w"> </span><span class="s2">&quot;pub,nan&quot;</span>
</code></pre></div>
<h3 id="mix-aggregated-group-and-individual-genome">Mix aggregated group and individual genome</h3>
<div class="highlight"><pre><span></span><code>obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>myindex<span class="w"> </span>--output<span class="w"> </span>out<span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--group<span class="w"> </span><span class="s2">&quot;A:group=A&quot;</span><span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--select<span class="w"> </span><span class="s2">&quot;A,Betula_nana--IGA-24-39&quot;</span>
</code></pre></div>
<h3 id="pure-column-projection-no-aggregation">Pure column projection (no aggregation)</h3>
<div class="highlight"><pre><span></span><code>obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>myindex<span class="w"> </span>--output<span class="w"> </span>out<span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--select<span class="w"> </span><span class="s2">&quot;Betula_nana--TROM-V-149986,Betula_nana--AG-P04-25-01&quot;</span>
</code></pre></div>
<h3 id="compose-with-filter">Compose with filter</h3>
<div class="highlight"><pre><span></span><code><span class="c1"># Step 1: keep only B. nana-specific k-mers</span>
obikmer<span class="w"> </span>filter<span class="w"> </span>myindex<span class="w"> </span>--output<span class="w"> </span>filtered<span class="w"> </span><span class="se">\</span>
<span class="w"> </span>--ingroup<span class="w"> </span><span class="s2">&quot;species=Betula_nana&quot;</span><span class="w"> </span>--outgroup<span class="w"> </span><span class="s2">&quot;*&quot;</span>
<span class="c1"># Step 2: aggregate genome columns by collection site</span>
obikmer<span class="w"> </span><span class="k">select</span><span class="w"> </span>filtered<span class="w"> </span>--output<span class="w"> </span>final<span class="w"> </span>--aggregate-by<span class="w"> </span>site
</code></pre></div>
<hr />
<h2 id="implementation-notes">Implementation notes</h2>
<p><code>select</code> does not rebuild the MPHF. Every partition is processed independently
(<code>PartitionRunner</code>), each writing its own output layers; no cross-partition
synchronisation is needed.</p>
<p>For each layer in each partition (<code>obikselect::select_layer::select_partition</code>):</p>
2026-08-15 20:56:29 +02:00
<ol>
<li><code>copy_layer_files</code> hard-links the source layer's kmer-identity files
(<code>mphf.bin</code>/<code>unitigs.bin</code>/<code>evidence.bin</code>/<code>unitigs.bin.idx</code>/
<code>fingerprint.bin</code>/<code>layer_meta.json</code>) into the destination — never a real
copy unless linking fails or <code>--force-copy</code> is given.</li>
<li>A new data matrix is built with M columns (M = number of output columns),
under a fresh <code>presence/</code>/<code>counts/</code> subdirectory (never touching the
source's own).</li>
<li><strong>Presence source (2026-08-28: <code>batch_presence_counts</code>)</strong>: one shared pass
over the source bit matrix computes every output group's presence count at
once — row-major native for a <code>Sparse</code> source (<code>for_each_genome_in_row</code>,
which has no column representation to read a <code>col_view</code> from at all — the
reason this replaced the old per-group loop, not just an optimisation of
it), deduplicated column-major (one <code>col_view</code> per <em>distinct referenced
column</em>, not per group) for <code>Columnar</code>/<code>Packed</code>. Every <code>AggOp</code> for a bit
matrix is then a cheap derivation of that one count vector (<code>sum</code> = the
count itself, <code>any</code>/<code>max</code> = <code>count ≥ 1</code>, <code>all</code>/<code>min</code> = <code>count == group
size</code>, <code>none</code> = <code>count == 0</code>) — see
<code>obikselect::select_layer::agg_result_from_count</code>.</li>
<li><strong>Count source</strong>: unchanged, one <code>col_view</code>-driven pass per output column
via <code>MatrixGroupOps</code><code>sum</code>/<code>min</code>/<code>max</code> are genuine per-value reductions
for a count matrix, not derivable from a single presence count the way
they are for a bit matrix.</li>
2026-08-15 20:56:29 +02:00
<li><code>index.meta</code> is rewritten with the new genome list and updated <code>with_counts</code>.</li>
</ol>
<h3 id="known-gap-not-yet-fixed-2026-08-28">Known gap (not yet fixed, 2026-08-28)</h3>
<p>Step 4 above still panics (<code>col_view() not available on Sparse
PersistentCompactIntMatrix</code>) if the source is a <strong>count</strong> index packed
sparse — <code>batch_presence_counts</code>' row-major treatment was only ported to the
bit-matrix (<code>Presence</code>) case, since that was the one actually blocking a real
benchmark run. <code>select</code>/<code>filter</code> on a sparse-packed count index still hits
this; the fix would follow the same shape (a <code>PersistentSparseCompactIntMatrix</code>
row-major decode, analogous to <code>for_each_genome_in_row</code>), just not done. Since
<code>obisys::numa::runner::PartitionRunner</code>'s panic-propagation fix (see
<code>architecture/numa_partition_runner.md</code>), this at least fails fast (process
panic, exit 101) instead of hanging.</p>
2026-08-15 20:56:29 +02:00
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