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DNA encoding
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Minimizer selection
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Central-position SNP distance (discussion)
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SuperKmer
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Kmer
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Chunk reader
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Construction pipeline
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obipipeline library
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On-disk storage
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MPHF selection
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Unitig evidence encoding
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Evidence elimination (discussion)
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obikindex layer tier
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PersistentCompactIntVec
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PersistentBitVec
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Merge command
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Merge parallelism & memory
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Kmer filtering
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Select command
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Select command
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Output destination
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Defining output columns
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Named groups — --group
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Per-group operator — --group-op
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Shorthand — --aggregate-by / --aggregate-op
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Column selection and ordering — --select
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Aggregation operators
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Behaviour for edge cases
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Examples
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Aggregate by metadata group, default operators
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Named groups with different operators
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Mix aggregated group and individual genome
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Pure column projection (no aggregation)
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Compose with filter
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Implementation notes
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Known gap (not yet fixed, 2026-08-28)
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obitaxonomy crate
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Benchmark: query-path testing
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Partition and layer caching (discussion)
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Sequences
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Kmer index
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NUMA-aware worker pools
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NUMA-aware partition runner
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Defining output columns
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Named groups — --group
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Per-group operator — --group-op
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Shorthand — --aggregate-by / --aggregate-op
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Column selection and ordering — --select
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Aggregation operators
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Behaviour for edge cases
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Examples
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Aggregate by metadata group, default operators
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Named groups with different operators
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Mix aggregated group and individual genome
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Pure column projection (no aggregation)
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Compose with filter
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Known gap (not yet fixed, 2026-08-28)
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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 > < input-index>
2026-08-28 14:14:22 +02:00
< span class = "w" > </ span > --output< span class = "w" > </ span > < dir>
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< span class = "w" > </ span >< span class = "o" > [</ span > --group< span class = "w" > </ span > < name> :< pred> < span class = "w" > </ span > ...< span class = "o" > ]</ span >
< span class = "w" > </ span >< span class = "o" > [</ span > --group-op< span class = "w" > </ span > < name> :< op> < span class = "w" > </ span > ...< span class = "o" > ]</ span >
< span class = "w" > </ span >< span class = "o" > [</ span > --aggregate-by< span class = "w" > </ span > < key> < span class = "w" > </ span >< span class = "o" > ]</ span >
< span class = "w" > </ span >< span class = "o" > [</ span > --aggregate-op< span class = "w" > </ span > < op> < span class = "w" > </ span >< span class = "o" > ]</ span >
< span class = "w" > </ span >< span class = "o" > [</ span > --select< span class = "w" > </ span > < col1,col2,...> < span class = "w" > </ span >< span class = "o" > ]</ span >
< span class = "w" > </ span >< span class = "o" > [</ span > --presence-threshold< span class = "w" > </ span > < N> < span class = "w" > </ span >< span class = "o" > ]</ span >
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< span class = "w" > </ span >< span class = "o" > [</ span > --force-copy< span class = "w" > </ span >< span class = "o" > ]</ span >
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</ code ></ pre ></ div >
< hr />
< h2 id = "output-destination" > Output destination</ h2 >
2026-08-28 14:14:22 +02:00
< p >< code > --output < dir> </ 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 && mv INDEX.tmp INDEX</ code > ) — the case
< code > --in-place</ code > used to cover.</ p >
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< 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 < name> :< pred>
</ 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" > " pub:species=Betula_pubescens" </ span >
--group< span class = "w" > </ span >< span class = "s2" > " nan:species=Betula_nana" </ 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 < name> :< op>
</ 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" > " pub:any" </ span >
--group-op< span class = "w" > </ span >< span class = "s2" > " nan:all" </ 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 < key> </ code > automatically creates one group per unique value of the
metadata key < code > < key> </ code > . Equivalent to one < code > --group < val> :< key> =< val> </ code > per distinct
value. < code > --aggregate-op < op> </ 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 > 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 " group" ; 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" > " pub:species=Betula_pubescens" </ span >< span class = "w" > </ span >< span class = "se" > \</ span >
< span class = "w" > </ span > --group< span class = "w" > </ span >< span class = "s2" > " nan:species=Betula_nana" </ span >< span class = "w" > </ span >< span class = "se" > \</ span >
< span class = "w" > </ span > --group-op< span class = "w" > </ span >< span class = "s2" > " pub:any" </ span >< span class = "w" > </ span >< span class = "se" > \</ span >
< span class = "w" > </ span > --group-op< span class = "w" > </ span >< span class = "s2" > " nan:all" </ span >< span class = "w" > </ span >< span class = "se" > \</ span >
< span class = "w" > </ span > --select< span class = "w" > </ span >< span class = "s2" > " pub,nan" </ 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" > " A:group=A" </ span >< span class = "w" > </ span >< span class = "se" > \</ span >
< span class = "w" > </ span > --select< span class = "w" > </ span >< span class = "s2" > " A,Betula_nana--IGA-24-39" </ 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" > " Betula_nana--TROM-V-149986,Betula_nana--AG-P04-25-01" </ 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" > " species=Betula_nana" </ span >< span class = "w" > </ span > --outgroup< span class = "w" > </ span >< span class = "s2" > " *" </ 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 >
2026-08-28 14:14:22 +02:00
< 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 >
2026-08-28 14:14:22 +02:00
< 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 >
2026-08-28 14:14:22 +02:00
< 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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