Documents a proposed redesign for cross-partition batch resolution, shifting trigger logic to per-destination accumulator thresholds and introducing entropy-based pruning criteria. Adds an `n_layers_per_partition` method to the index, exposing partition metadata with consistent error handling and clarified documentation regarding build-time structural properties.
16 KiB
Sibling annex — architecture (discussion)
Status: architecture decided (2026-08-14). Implementation not yet mandated.
Two index spaces, uncorrelated
Every kmer stored in a Layer lives in two independent index spaces:
- Iteration order: its position when enumerating
unitigs.bin(the superkmer file), deterministic but arbitrary with respect to slot. - MPHF slot:
MphfLayer::index(kmer), the number the MPHF assigns.
The two are not correlated by any formula. Converting from one to the other
requires either recomputing the MPHF (kmer → slot) or scanning the iteration
stream (kmer → order). There is no slot → kmer operation: the MPHF is a
one-way function, not an invertible bijection with a stored inverse. Any
method that reconstructs a kmer from a bare slot number is wrong by
construction, regardless of the mechanism used (MPHF re-hash, or evidence
decode + direct unitig read). See MphfLayer::kmer_at
(obilayeredmap/src/mphf_layer.rs) — flagged for removal, currently called
from obikphylo/siblings/build.rs and family_scan.rs (since removed — see
"Pending work" status below).
Two pipelines, never mixed
| origin of the kmer | membership known? | correct mapping | |
|---|---|---|---|
| query pipeline | external (caller-supplied) | no | query/find/find_strict — MPHF + evidence check |
| iteration pipeline | enumerated from this layer's own unitigs.bin |
yes, by construction | index/index_batch — MPHF only, no evidence |
Evidence exists solely to answer "is this external kmer a member of the
layer" for the query pipeline. Using it (or the MPHF) to go the other way —
recover a kmer from a slot, or re-verify a kmer that was just produced by
iterating the layer — is a conceptual error: evidence can be probabilistic
(Approx mode), so any slot→kmer attempt is unsound in general, and
pointless even in Exact/Hybrid mode since the kmer was already known.
Sibling annex: an iteration-pipeline artifact only
The sibling annex (FamilyMask/SiblingAnnex, .psib,
obicompactvec/src/siblingannex.rs) records, per kmer, whether it is a
family minorant and which family members are present in the index. Its only
consumers (obikphylo/siblings/stats.rs, family_scan.rs) enumerate it
exhaustively (0..annex.len()); no query-pipeline code path touches it.
Decision: the annex must be persisted in iteration order, not slot
order. This lets readers zip-iterate Layer::iter_kmers() and the annex
file directly — one linear, cache-friendly pass, no MPHF/slot indirection,
no kmer_at. It also enables specialized iterators building on this zip:
minorants-only iteration, batch-of-kmers → batch-of-family-members, etc.
Today the annex is built and stored in slot order
(build_layer_sibling_annex, siblings/build.rs): slot_kmer is populated
via (0..n_slots).map(|slot| mphf.kmer_at(slot)), and the origin slot is
threaded through the whole cross-partition reconciliation pipeline (variant
generation, query_partition_with, final mask[slot].fetch_or(...)). This
must change to iterating iter_kmers()/enumerate_kmers() and threading
the iteration index instead of the slot end to end — eliminating
kmer_at from the build path entirely, not just the read path. No
slot-indexed intermediate is needed even during construction; the
iteration-order id is sufficient throughout.
The cross-partition side of the same pipeline is unaffected: checking
whether a generated family-variant kmer exists in another partition is a
genuine query-pipeline operation (the variant's membership in the target
partition is unknown) and must keep going through
KmerPartition::query_partition_with (MPHF + evidence), never a raw
index().
Pending work — done
The plan above shipped: obikphylo (a new crate — phylo-domain extension
traits over obikindex::KmerIndex/obilayeredmap::Layer<D>, replacing the
old obikindex::siblings module) builds and reads the annex purely in
iteration order (SiblingLayerExt::iter_siblings/iter_minorants, both with
batch variants, mirroring Layer<D>'s own KmerIter/KmerBatchIter
shape). MphfLayer::kmer_at has no remaining callers.
A separate, unrelated bug surfaced during this work and was fixed
(2026-08-14): MphfLayer::enumerate_kmers_batch computed its
batch_start_index via the stdlib .enumerate() adapter, which counts
batches (0, 1, 2…), not the cumulative k-mer offset the annex is actually
keyed on — every batch past the first wrote its mask/annex entries at the
wrong iteration-order position. Fixed by tracking a running offset instead;
regression tests added (sibling_annex_no_empty_masks_after_build,
sibling_histogram_does_not_panic_on_partial_last_batch).
Performance: build_sibling_annex parallelism (2026-08-14)
Investigated on a real multi-genome run (phyloskims_sal_vac, k=31/m=11).
Baseline: mostly one active core, with short multi-core bursts — average
~3 cores.
Fixes that helped, kept:
CanonicalKmerOf::minimizer()(obikseq/src/kmer.rs) — a direct O(k) bit-arithmetic minimiser for a single isolated k-mer, replacing aRollingStatinstance fed byte-by-byte through an ASCII round-trip (used byhelpers::partition_of, called for every generated family variant). ~3x wall-clock improvement on its own, confirmed by sampling (obiskbuilder::rolling_stat/obikentropyframes disappeared from the hot path).CanonicalKmerOf::partition()added alongside it (wrapsminimizer().seq_hash() & mask, the same routing ruleKmerPartition/RoutableSuperKmeruse).- Cross-partition resolution (
outgoing.par_iter()inbuild_layer_sibling_annex) parallelised at the partition level — one Rayon task per non-emptyoutgoing[dest]bucket. For k=31/m=11, a central-base substitution changes the winning minimiser (and thus the destination partition) only when that window overlaps the central base: ~11 of the 21 possible windows do, so ~10/21 (≈48%) of generated variants route right back to the partition already being built. That self bucket ends up far larger than any other, so the per-partition split pinned one thread to it alone while the rest of the pool finished instantly — confirmed by sampling: one thread solid inMphfLayer::find, everyone else idle. Fixed by splitting each non-empty bucket intototal_queries / n_workers(capped 4096) chunks beforepar_iter(), preserving per-partition mmap locality (each chunk stays contiguous within one partition) while letting Rayon spread an oversized bucket across several threads. Net effect of both fixes together: ~3 cores average → ~10-13 cores average on the same run, and a projected total build time of ~1h15 down to ~30min on the realphyloskims_sal_vacrun this was measured against. TracedBar's ETA (obisys/src/progress.rs) was silently starved: the custom progress message and the self-computed ETA text used to share onepb.set_message()slot, with the ETA holding off for 2s after any custom message — fine when custom messages are rare, broken oncebuild_sibling_annex's per-partition callback fires more often than that. Fixed by keeping the two texts in separate fields, composed together on every render instead of one overwriting the other.
Tried and reverted — do not repeat blindly:
- Parallelising the outer partition loop in
build_sibling_annexwithobikindex::PartitionRunner(already used bymerge/build_layers), splitting a fixed core budget between outer (partition) and inner (pipeline + resolution) concurrency so their product wouldn't exceed the budget. Measured worse: throughput dropped over time (26 partitions/5min → 38/11-12min) and peak resolution concurrency fell from ~11-12 cores to ~7-8. Cause: this capped the resolution burst — which scales very well on its own — to make room for outer concurrency, and running several partitions' resolution at once scatters access across multiple partitions' mmap regions at once, working against the localityoutgoing's per-partition grouping exists for.PartitionRunnerstayed exported fromobikindex(new_cappedtoo) since it's general-purpose, but nothing inobikphylocalls it. - Splitting resolution chunks even finer (
/(n_workers*8), cap 1024, instead of/n_workers, cap 4096) to smooth the residual sawtooth. Measured ~10% slower, wider dips, not narrower. Reverted to the original chunk sizing.
Cross-partition batch resolution — current state vs. the batched-accumulator design (discussion, 2026-08-14)
family_scan.rs::scan_layer_families (shared by snp_pseudo_alignment,
sibling_annex_stats, cardinality_tally, scan_family_pairs) already
implements most of a dispatch/accumulate/resolve pipeline: generation
(cheap, CPU-only — builds outgoing[dest_partition] from FamilyMask and
buckets cross-partition queries) runs on an obipipeline::throttle +
make_pipe! stage, decoupled from resolution (I/O-bound, rayon::par_iter
across partitions, one generated batch resolved at a time, never several
concurrently — this ordering is deliberate, see the module's own docs on a
reverted concurrent-batch-resolution attempt that scattered mmap access).
The fast/slow mode gate (PartitionCache::fast_mode, cache.rs:162-163)
already exists: n_layers <= 7 (checked once from the first non-empty
partition's PartitionMeta::n_layers, documented as identical across every
partition of an index — a structural, build-time property, never a
per-partition state) decides whether FamilyMask's recorded layer_value
can be trusted to skip straight to the right layer
(find_presence_batch_fast) or must fall back to scanning every layer of
the destination partition (find_presence_batch).
Real gap, confirmed not implemented: resolution is triggered by the
source batch finishing (FAMILY_BATCH = 65536 minorants read from the
scanned layer), not by an output accumulator filling up. Since most
central-base variants of a family route back to the same partition being
scanned (~48% per the k=31/m=11 measurement above), a FAMILY_BATCH's
outgoing[dest] is large for the local/self partition and thin for the
other ~255 (or however many) destination partitions — each of those gets
resolved at low query density every batch instead of being accumulated
across several source batches until resolving it is worthwhile. This is
distinct from, and not fixed by, the fast/slow layer gate above.
Redesign sketched (not built): per-destination accumulators decoupled from
FAMILY_BATCH, flushed on reaching a size threshold instead of on source-batch
completion — a "hot" accumulator for the partition being scanned (sharded
one-per-generation-worker, no lock, since all n_workers pipeline workers
write to it concurrently — this differs from an earlier, simpler mental
model of "one thread owns one layer's local collector," which doesn't hold
here since n_workers threads cooperate on scanning one layer at a time,
not one thread per layer) and "cold" mutex-per-partition accumulators for
the rest, low contention expected since traffic to any single cold
destination is a small fraction of total.
This breaks the current strict-iteration-order delivery of on_family
(today: a reorder buffer keyed by batch, since a whole FAMILY_BATCH
resolves atomically). With cross-batch accumulation, a family only becomes
complete once every accumulator holding one of its outgoing queries has
flushed, at unpredictable, independent times — no longer streamable
strictly in order without a large, unbounded pending buffer. Resolution
sketched: replace order-dependent consumers with coordinate-addressed
writes instead of order-dependent appends (see PseudoAlignment idea
below) wherever possible, since sibling_annex_stats's reduction (plain
counts) is already order-independent and needs nothing here.
Pseudo-alignment at scale — pruning is unavoidable (discussion, 2026-08-14)
The reference run (phyloskims_sal_vac-scale bacterial test set,
iqtree.fasta) produced a dense alignment for 13 genomes × 383,965 sites
(4.8 MB) — trivially small. The in-progress plant index is expected to
carry on the order of 9 billion minorant families; a dense byte-per-cell
alignment at that column count is unbuildable regardless of genome count
(hundreds of GB even at a handful of genomes). Long-term ambition is 6,000–
8,000 genomes on a large machine, which makes the per-cell cost dominant in
the other dimension too. Pruning the retained family set before
materializing anything is mandatory, not an optimization.
Already free: family_size() < 2 (no sibling variant registered at
all) is a zero-cost structural filter, read directly off FamilyMask bits,
already applied in snp_pseudo_alignment. Insufficient alone — per the
~80-85% mono-family estimate from earlier discussion, this only brings 9
billion down to roughly 1.3-1.8 billion, still unusable.
Criterion under discussion: fix a global cell budget
(n_genomes × n_columns_retained ≤ threshold) and retain the
highest-entropy families first until the budget is spent — column count
self-adjusts to genome count automatically. Entropy of a family: Shannon
entropy over the observed base distribution across genomes carrying that
family, decided 2026-08-14: genomes where the family is absent are
excluded from the calculation (denominator = genomes where present, not
all genomes) — measures signal purity where it exists, independent of
coverage rate.
Key consequence for storage: entropy needs per-variant genome counts, which
cannot be derived from FamilyMask's bits alone — it requires the same
cross-partition resolution work the alignment/stats pipeline already pays
for. This favors computing it once at annex-build time and persisting it in
an auxiliary vector alongside the annex (one value per retained
minorant) over encoding a fixed keep/discard decision as one of
FamilyMask's 3 remaining free bits (bits 13-15, siblingannex.rs:77): the
bit approach bakes a single threshold in permanently (any different budget
needs a full annex rebuild), the vector approach pays the expensive
resolution once and lets budget/threshold be chosen freely per analysis
afterward.
Open, explicitly deferred: scope of the top-K selection — global across the whole index (needs a first pass computing/storing every family's entropy, then a global threshold from the full distribution, e.g. a quantile, before building the final alignment: two full passes, but the size budget is honored precisely) vs. local per layer/partition (stays within the current single-pass streaming model, but the global budget is no longer exactly guaranteed — depends on how unevenly entropy is distributed across layers).
Known remaining limitation, not yet worth fixing: within one layer, the
four stages (sequential unitigs.bin read → parallel generation →
parallel resolution → sequential annex write) never overlap — confirmed by
1s-interval sampling: generation alone occupies ~17 threads evenly, but the
next layer's read/generation never starts until the current layer's
resolution and write are both done. This produces a real, periodic (~layer
duration) alternation between "many cores" and "few cores" that neither of
the fixes above touches, since both operate within one layer's resolution
step. The only remaining lever is overlapping consecutive layers (e.g. a
depth-2 pipeline: start layer N+1's read/generation while layer N's
resolution/write is still running) — a real restructuring, not a parameter
tweak, and explicitly not to be combined with the reverted
budget-capping idea above (let each phase use however many cores it
naturally wants; only the scheduling needs to overlap). Deferred, not
started.