diff --git a/Home.md b/Home.md
index a2a725b..2ef75f1 100644
--- a/Home.md
+++ b/Home.md
@@ -15,7 +15,7 @@ All functionality is exposed through a single binary, `obikmer`, organized as su
 ## Commands
 
 | Command | Purpose |
-|---|---|
+| --- | --- |
 | [`superkmer`](usage-superkmer) | Extract super-kmers from a sequence file and write them to stdout |
 | [`index`](usage-index_command) | Build a genome index |
 | [`merge`](usage-merge) | Merge multiple indexes into one |
@@ -48,7 +48,7 @@ See [Genome predicates and taxonomy paths](usage-predicates) for the selection l
 These constraints are checked at startup; an invalid value exits immediately with an error.
 
 | Parameter | Constraint | Reason |
-|---|---|---|
+| --- | --- | --- |
 | $k$ (`--kmer-size`) | odd, $k \in [11, 31]$ | odd length guarantees the canonical form is always well defined; the range keeps a kmer within a 64-bit word while retaining specificity |
 | $m$ (`--minimizer-size`) | odd, $3 \le m \le k-1$ | same palindrome argument as $k$; must be strictly shorter than the kmer |
 | $z$ (`-z`, approximate evidence only) | $z \le k-1$ | the effective indexed kmer size is $k-z+1$ |
@@ -58,7 +58,7 @@ These constraints are checked at startup; an invalid value exits immediately wit
 Genome labels are arbitrary Unicode strings, with the following restrictions:
 
 | Character | Forbidden | Reason |
-|---|---|---|
+| --- | --- | --- |
 | `/` | yes | filesystem path separator |
 | `=` | yes | separator used by `--new-label` |
 | `\0` | yes | null byte |
diff --git a/formats-index_layout.md b/formats-index_layout.md
index 0960f0d..3da36d6 100644
--- a/formats-index_layout.md
+++ b/formats-index_layout.md
@@ -26,26 +26,24 @@ Two verification modes are available, selected at build time (`index --approx`)
 
 ## On-disk layout
 
-```
-<index_root>/
-  index.meta                    global configuration (k, minimizer size, partition count,
-                                 evidence mode, whether counts are stored) and genome list/metadata
-  scatter.done / count.done / index.done      build-progress sentinels
-  spectrums/<label>.json        per-genome kmer frequency histogram
-  partitions/
-    part_00000/ ... part_NNNNN/
-      index/
-        meta.json                number of layers in this partition
-        layer_0/
-          unitigs.bin             reconstructible kmer sequence data — always kept
-          unitigs.bin.idx         random-access index into unitigs.bin (exact evidence only)
-          mphf.bin                 the minimal perfect hash function
-          evidence.bin              exact evidence (exact mode only)
-          fingerprint.bin           approximate evidence (approximate mode only)
-          counts/                   per-genome kmer counts (if counts were requested)
-          presence/                 per-genome presence/absence bits
-        layer_1/, layer_2/, ...     added by later merges, same internal structure
-```
+    <index_root>/
+      index.meta                    global configuration (k, minimizer size, partition count,
+                                     evidence mode, whether counts are stored) and genome list/metadata
+      scatter.done / count.done / index.done      build-progress sentinels
+      spectrums/<label>.json        per-genome kmer frequency histogram
+      partitions/
+        part_00000/ ... part_NNNNN/
+          index/
+            meta.json                number of layers in this partition
+            layer_0/
+              unitigs.bin             reconstructible kmer sequence data — always kept
+              unitigs.bin.idx         random-access index into unitigs.bin (exact evidence only)
+              mphf.bin                 the minimal perfect hash function
+              evidence.bin              exact evidence (exact mode only)
+              fingerprint.bin           approximate evidence (approximate mode only)
+              counts/                   per-genome kmer counts (if counts were requested)
+              presence/                 per-genome presence/absence bits
+            layer_1/, layer_2/, ...     added by later merges, same internal structure
 
 `unitigs.bin` is the only file from which the indexed kmer content can be fully recovered; it is always retained. Every other file (MPHF, evidence, counts) is derived from it.
 
diff --git a/theory-encoding.md b/theory-encoding.md
index 80230a9..22a1c7e 100644
--- a/theory-encoding.md
+++ b/theory-encoding.md
@@ -5,11 +5,11 @@
 Every nucleotide is encoded on 2 bits, most-significant-bit first within each word:
 
 | Base | Encoding |
-|------|----------|
-| A    | `00`     |
-| C    | `01`     |
-| G    | `10`     |
-| T    | `11`     |
+| --- | --- |
+| A | `00` |
+| C | `01` |
+| G | `10` |
+| T | `11` |
 
 The Watson-Crick complement of a base is its bitwise NOT on 2 bits: $\text{complement}(base) = \lnot base \mathbin{\&} \texttt{0b11}$.
 
diff --git a/theory-entropy_filter.md b/theory-entropy_filter.md
index 416baa5..09ee744 100644
--- a/theory-entropy_filter.md
+++ b/theory-entropy_filter.md
@@ -22,7 +22,7 @@ A value near 0 indicates low complexity (e.g. a homopolymer run); near 1 indicat
 
 ## Final score
 
-The filter evaluates $\hat{H}(ws)$ for every word size from 1 to ws_max and keeps the minimum:
+The filter evaluates $\hat{H}(ws)$ for every word size from 1 to ws\_max and keeps the minimum:
 
 $$\text{entropy}(kmer) = \min_{ws=1}^{ws_{\max}} \hat{H}(ws)$$
 
diff --git a/theory-indexing_architecture.md b/theory-indexing_architecture.md
index ca0e9fc..fa492cd 100644
--- a/theory-indexing_architecture.md
+++ b/theory-indexing_architecture.md
@@ -6,9 +6,7 @@ An index is split into a fixed number of **partitions**, each handling an indepe
 
 The canonical minimizer of a super-kmer (see [Minimizer selection](theory-minimizer_selection)) is hashed to produce a $p$-bit routing value that selects the destination partition:
 
-```
-canonical minimizer → hash(minimizer) → p-bit value → partition index
-```
+    canonical minimizer → hash(minimizer) → p-bit value → partition index
 
 Within a partition, kmers are indexed as plain values via a minimal perfect hash function (see [On-disk storage](formats-index_layout)); the minimizer plays no further role once a super-kmer has reached its partition.
 
@@ -17,10 +15,10 @@ Within a partition, kmers are indexed as plain values via a minimal perfect hash
 Even though $H$ already makes minimizer values well-distributed (see [Minimizer selection](theory-minimizer_selection)), choosing $p$ well below the number of bits available in the minimizer ($2m$) leaves a comfortable entropy margin, provided the number of distinct minimizers actually observed is much larger than the number of partitions.
 
 | Minimizer size $m$ | Minimizer bits ($2m$) | Typical partition-index bits $p$ | Partitions |
-|----|-----------|-----------|------------|
-| 9  | 18        | 6–8       | 64–256     |
-| 11 | 22        | 8–10      | 256–1 024  |
-| 13 | 26        | 10–12     | 1 024–4 096|
-| 15 | 30        | 10–14     | 1 024–16 384|
+| --- | --- | --- | --- |
+| 9 | 18 | 6–8 | 64–256 |
+| 11 | 22 | 8–10 | 256–1 024 |
+| 13 | 26 | 10–12 | 1 024–4 096 |
+| 15 | 30 | 10–14 | 1 024–16 384 |
 
 The number of partitions must satisfy $p \le 2m$, and in practice $p$ is chosen well below that bound to leave a comfortable entropy margin. For $k=31$, $m=13$, $p=10$ (1024 partitions), partition load is well balanced on real genomic data.
diff --git a/theory-kmers_and_superkmers.md b/theory-kmers_and_superkmers.md
index 7e01796..c7aadbe 100644
--- a/theory-kmers_and_superkmers.md
+++ b/theory-kmers_and_superkmers.md
@@ -11,7 +11,7 @@ A **kmer** is a DNA subsequence of fixed length $k$. Two constraints apply to $k
 
 A **super-kmer** is a maximal run of consecutive, overlapping kmers from a read that share the same canonical minimizer (see [Minimizer selection](theory-minimizer_selection)). Each kmer in the run overlaps the next by $k-1$ nucleotides. A super-kmer is capped at 256 nucleotides; a longer run is split at that boundary.
 
-For a random minimizer of length $m$ over kmers of length $k$, the expected length of a super-kmer is approximately ([Golan & Shur 2025](#ref-Golan2025-xf); [Zheng *et al.* 2020](#ref-Zheng2020-ji)):
+For a random minimizer of length $m$ over kmers of length $k$, the expected length of a super-kmer is approximately ([Golan & Shur 2025](#ref-Golan2025-xf); [Zheng et al. 2020](#ref-Zheng2020-ji)):
 
 $$L_{\text{nt}} \approx \frac{k-m+2}{2} + k - 1$$
 
@@ -25,17 +25,17 @@ Super-kmers are the unit of work used throughout construction and querying: sequ
 
 ## Bibliography
 
-<div id="refs" class="references csl-bib-body hanging-indent" data-entry-spacing="0">
+<div id="refs" class="references csl-bib-body hanging-indent">
 
 <div id="ref-Golan2025-xf" class="csl-entry">
 
-Golan, S. & Shur, A.M. (2025). [Expected density of random minimizers](https://doi.org/10.1007/978-3-031-82670-2\_25). In: *Lecture notes in computer science*, Lecture notes in computer science. Springer Nature Switzerland, Cham, pp. 347–360.
+Golan, S. & Shur, A.M. (2025). <a href="https://doi.org/10.1007/978-3-031-82670-2\_25">Expected density of random minimizers</a>. In: <span style="font-style: italic;">Lecture Notes in Computer Science</span>, Lecture Notes in Computer Science. Springer Nature Switzerland, Cham, pp. 347–360.
 
 </div>
 
 <div id="ref-Zheng2020-ji" class="csl-entry">
 
-Zheng, H., Kingsford, C. & Marçais, G. (2020). [Improved design and analysis of practical minimizers](https://doi.org/10.1093/bioinformatics/btaa472). *Bioinformatics (Oxford, England)*, 36, i119–i127.
+Zheng, H., Kingsford, C. & Marçais, G. (2020). <a href="https://doi.org/10.1093/bioinformatics/btaa472">Improved design and analysis of practical minimizers</a>. <span style="font-style: italic;">Bioinformatics (Oxford, England)</span>, 36, i119–i127.
 
 </div>
 
diff --git a/theory-minimizer_selection.md b/theory-minimizer_selection.md
index f171b63..6b83a47 100644
--- a/theory-minimizer_selection.md
+++ b/theory-minimizer_selection.md
@@ -8,7 +8,7 @@ The minimizer partitions a sequence into super-kmers: maximal runs of overlappin
 
 ## Hash-based ("random") minimizer
 
-`obikmer` selects minimizers by hash order rather than plain lexicographic order. Ordering m-mers lexicographically on their 2-bit encoding systematically favors AT-rich m-mers (an all-A m-mer always encodes to 0), which causes low-complexity regions to dominate as minimizers and produces unbalanced partitions ([Golan & Shur 2025](#ref-Golan2025-xf); [Kille *et al.* 2023](#ref-Kille2023-px); [Pan & Reinert 2024](#ref-Pan2024-hb); [Zheng *et al.* 2020](#ref-Zheng2020-ji), [2021](#ref-Zheng2021-cc)).
+`obikmer` selects minimizers by hash order rather than plain lexicographic order. Ordering m-mers lexicographically on their 2-bit encoding systematically favors AT-rich m-mers (an all-A m-mer always encodes to 0), which causes low-complexity regions to dominate as minimizers and produces unbalanced partitions ([Golan & Shur 2025](#ref-Golan2025-xf); [Kille et al. 2023](#ref-Kille2023-px); [Pan & Reinert 2024](#ref-Pan2024-hb); [Zheng et al. 2020](#ref-Zheng2020-ji); [2021](#ref-Zheng2021-cc)).
 
 Instead, a well-distributed hash function $H$ is applied to the canonical (lexicographically minimal) form of each m-mer, and the m-mer with the smallest $H$ value wins. Because $H$ is a bijection with good avalanche properties, every distinct m-mer in a window has an equal chance of holding the minimum hash value, independent of its nucleotide composition.
 
@@ -24,7 +24,7 @@ The hash function is a 64-bit mixing function (splitmix64-style finalizer) appli
 
 $$H(x) = \text{mix64}(x \oplus s)$$
 
-``` text
+```text
 H(x):
     x ← x  ⊕  s
     x ← x  ⊕  (x >> 30)
@@ -36,15 +36,15 @@ H(x):
 
 The choice of $s$ is not arbitrary. Low-complexity m-mers (homopolymers, short tandem repeats) are disproportionately abundant in real genomes; if one of them happened to be the perpetual argmin of $H$ — as the all-A m-mer is when $s = 0$, since $\text{mix64}(0) = 0$ is a fixed point — it would win far more windows than the composition-uniform behavior established above predicts, not because $H$ favors it, but because that pathological input keeps recurring in real sequence data. Exhaustive checks confirm that, with this seed, the argmin is never a homopolymer or any periodic repeat, for every tested $m$:
 
-| $m$ | argmin (canonical) | decoded sequence  | minimal period |
-|-----|--------------------|-------------------|----------------|
-| 3   | 16                 | `CAA`             | 3              |
-| 5   | 78                 | `ACATG`           | 5              |
-| 7   | 5512               | `CCCGAGA`         | 7              |
-| 9   | 108760             | `CGGGATCGA`       | 9              |
-| 11  | 179014             | `AAGGTGTCACG`     | 11             |
-| 13  | 33759044           | `GAAATACTTCACA`   | 13             |
-| 15  | 29869313           | `AACTACTTACCAAAC` | 15             |
+| $m$ | argmin (canonical) | decoded sequence | minimal period |
+| --- | --- | --- | --- |
+| 3 | 16 | `CAA` | 3 |
+| 5 | 78 | `ACATG` | 5 |
+| 7 | 5512 | `CCCGAGA` | 7 |
+| 9 | 108760 | `CGGGATCGA` | 9 |
+| 11 | 179014 | `AAGGTGTCACG` | 11 |
+| 13 | 33759044 | `GAAATACTTCACA` | 13 |
+| 15 | 29869313 | `AACTACTTACCAAAC` | 15 |
 
 If the minimum period length is found to be $m$ as observed in the above table, then the sequence is aperiodic, as no shorter period can be identified.
 
@@ -58,35 +58,35 @@ See [Partitioning and indexing architecture](theory-indexing_architecture) for m
 
 ## Bibliography
 
-<div id="refs" class="references csl-bib-body hanging-indent" data-entry-spacing="0">
+<div id="refs" class="references csl-bib-body hanging-indent">
 
 <div id="ref-Golan2025-xf" class="csl-entry">
 
-Golan, S. & Shur, A.M. (2025). [Expected density of random minimizers](https://doi.org/10.1007/978-3-031-82670-2\_25). In: *Lecture notes in computer science*, Lecture notes in computer science. Springer Nature Switzerland, Cham, pp. 347–360.
+Golan, S. & Shur, A.M. (2025). <a href="https://doi.org/10.1007/978-3-031-82670-2\_25">Expected density of random minimizers</a>. In: <span style="font-style: italic;">Lecture Notes in Computer Science</span>, Lecture Notes in Computer Science. Springer Nature Switzerland, Cham, pp. 347–360.
 
 </div>
 
 <div id="ref-Kille2023-px" class="csl-entry">
 
-Kille, B., Garrison, E., Treangen, T.J. & Phillippy, A.M. (2023). [Minmers are a generalization of minimizers that enable unbiased local jaccard estimation](https://doi.org/10.1093/bioinformatics/btad512). *Bioinformatics (Oxford, England)*, 39.
+Kille, B., Garrison, E., Treangen, T.J. & Phillippy, A.M. (2023). <a href="https://doi.org/10.1093/bioinformatics/btad512">Minmers are a generalization of minimizers that enable unbiased local Jaccard estimation</a>. <span style="font-style: italic;">Bioinformatics (Oxford, England)</span>, 39.
 
 </div>
 
 <div id="ref-Pan2024-hb" class="csl-entry">
 
-Pan, C. & Reinert, K. (2024). [A simple refined DNA minimizer operator enables 2-fold faster computation](https://doi.org/10.1093/bioinformatics/btae045). *Bioinformatics (Oxford, England)*, 40.
+Pan, C. & Reinert, K. (2024). <a href="https://doi.org/10.1093/bioinformatics/btae045">A simple refined DNA minimizer operator enables 2-fold faster computation</a>. <span style="font-style: italic;">Bioinformatics (Oxford, England)</span>, 40.
 
 </div>
 
 <div id="ref-Zheng2020-ji" class="csl-entry">
 
-Zheng, H., Kingsford, C. & Marçais, G. (2020). [Improved design and analysis of practical minimizers](https://doi.org/10.1093/bioinformatics/btaa472). *Bioinformatics (Oxford, England)*, 36, i119–i127.
+Zheng, H., Kingsford, C. & Marçais, G. (2020). <a href="https://doi.org/10.1093/bioinformatics/btaa472">Improved design and analysis of practical minimizers</a>. <span style="font-style: italic;">Bioinformatics (Oxford, England)</span>, 36, i119–i127.
 
 </div>
 
 <div id="ref-Zheng2021-cc" class="csl-entry">
 
-Zheng, H., Kingsford, C. & Marçais, G. (2021). [Sequence-specific minimizers via polar sets](https://doi.org/10.1093/bioinformatics/btab313). *Bioinformatics (Oxford, England)*, 37, i187–i195.
+Zheng, H., Kingsford, C. & Marçais, G. (2021). <a href="https://doi.org/10.1093/bioinformatics/btab313">Sequence-specific minimizers via polar sets</a>. <span style="font-style: italic;">Bioinformatics (Oxford, England)</span>, 37, i187–i195.
 
 </div>
 
diff --git a/usage-annotate.md b/usage-annotate.md
index 4734657..5a1329e 100644
--- a/usage-annotate.md
+++ b/usage-annotate.md
@@ -10,13 +10,13 @@ obikmer annotate INDEX --dump
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory to annotate (modified in place) |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--csv` | — | CSV file of metadata to apply (must contain an id column); required unless `--dump` is used |
 | `--sep` | `,` | CSV field separator |
 | `--id-col` | `id` | Name of the column containing genome labels |
diff --git a/usage-convert.md b/usage-convert.md
index f85632d..828c530 100644
--- a/usage-convert.md
+++ b/usage-convert.md
@@ -9,7 +9,7 @@ obikmer convert INDEX (--exact-evidence | --approx-evidence BITS | --hybrid-evid
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory to convert (modified in place) |
 
 ## Options
@@ -17,7 +17,7 @@ obikmer convert INDEX (--exact-evidence | --approx-evidence BITS | --hybrid-evid
 Exactly one of the first three is required:
 
 | Option | Description |
-|---|---|
+| --- | --- |
 | `--exact-evidence` | Convert to exact evidence (zero false positives) |
 | `--approx-evidence BITS` | Convert to approximate (fingerprint-only) evidence; `BITS` = fingerprint bits per slot (b) |
 | `--hybrid-evidence` | Convert to hybrid evidence (both exact and approximate bundles kept) |
diff --git a/usage-dump.md b/usage-dump.md
index 8b7873c..9bece57 100644
--- a/usage-dump.md
+++ b/usage-dump.md
@@ -9,13 +9,13 @@ obikmer dump INDEX [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory to dump |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--force-presence` | off | Output presence/absence (0/1) even if the index stores counts |
 | `--debug` | off | Prefix each row with the partition and layer columns |
 | `--head N` | none | Limit output to the first N kmers |
diff --git a/usage-estimate.md b/usage-estimate.md
index a8f326f..cfd76a6 100644
--- a/usage-estimate.md
+++ b/usage-estimate.md
@@ -9,7 +9,7 @@ obikmer estimate [OPTIONS]
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `-k, --kmer-size` | `31` | Kmer size used at query time (matches `index`'s `--kmer-size`) |
 | `-z, --findere-z` | none | Findere z parameter |
 | `--evidence-bits` | none | Fingerprint bits per slot (b) |
diff --git a/usage-filter.md b/usage-filter.md
index be0c1c8..e91f391 100644
--- a/usage-filter.md
+++ b/usage-filter.md
@@ -9,13 +9,13 @@ obikmer filter SOURCE -o OUTPUT [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `SOURCE` | Source index directory |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `-o, --output` | — (required) | Output index directory |
 | `-f, --force` | off | Overwrite an existing output directory |
 | `--presence` | off | Output presence/absence instead of counts |
@@ -27,7 +27,7 @@ obikmer filter SOURCE -o OUTPUT [OPTIONS]
 ## Predicate options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--ingroup` | none | Ingroup predicate (repeatable; each occurrence is ANDed) |
 | `--outgroup` | none | Outgroup predicate (repeatable; each occurrence is ORed) |
 | `--min-count` | 0, or group size + N if negative | Minimum number of ingroup genomes carrying the kmer |
diff --git a/usage-index_command.md b/usage-index_command.md
index 71a5cd2..6269e7c 100644
--- a/usage-index_command.md
+++ b/usage-index_command.md
@@ -9,18 +9,18 @@ obikmer index -o OUTPUT [OPTIONS] [INPUTS...]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INPUTS...` | Input sequence files or directories (FASTA/FASTQ/GenBank, gzip optional). If omitted, reads from stdin. |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `-o, --output` | — (required) | Output index directory |
 | `--force` | off | Overwrite an existing output directory |
 | `--label` | input file name without extension | Genome label stored in the index |
 | `--meta KEY=VALUE` | none | Attach a categorical metadata field to the genome (repeatable) |
-| `-k, --kmer-size` | `31` | Kmer size (odd, in [11, 31]) |
+| `-k, --kmer-size` | `31` | Kmer size (odd, in \[11, 31\]) |
 | `-m, --minimizer-size` | `11` | Minimizer size (odd, in $[3, k-1]$) |
 | `--theta` | `0.7` | Entropy threshold for the low-complexity filter |
 | `--level-max` | `6` | Maximum sub-word size for the entropy score |
diff --git a/usage-merge.md b/usage-merge.md
index 4e1dd8b..92f4f06 100644
--- a/usage-merge.md
+++ b/usage-merge.md
@@ -9,13 +9,13 @@ obikmer merge -o OUTPUT SOURCE... [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `SOURCE...` | Index directories to merge (at least one required) |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `-o, --output` | — (required) | Output index directory |
 | `--force` | off | Overwrite an existing output directory |
 | `--force-presence` | off | Store the merged index as presence/absence even if all sources have counts |
diff --git a/usage-pack.md b/usage-pack.md
index cdffa70..0a8260e 100644
--- a/usage-pack.md
+++ b/usage-pack.md
@@ -9,13 +9,13 @@ obikmer pack INDEX [--sparse]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory to pack (modified in place) |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--sparse` | off | Pack presence/absence and count matrices into a sparse, deduplicated format instead of the dense one |
 
 The index directory is locked for exclusive access while packing.
diff --git a/usage-phylo.md b/usage-phylo.md
index 67fbdcd..577abae 100644
--- a/usage-phylo.md
+++ b/usage-phylo.md
@@ -9,13 +9,13 @@ obikmer phylo INDEX [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory |
 
 ## Distance matrix (`--distance`)
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--distance` | `jaccard` | See the two tables below for the full list of accepted values |
 | `--gamma-shape ALPHA\|auto` | none | Rate-heterogeneity correction, for `snp-*` values that support it (see below). Either a fixed $\alpha$ or `auto`/`estimate` to fit it from the data (see "Automatic $\alpha$ estimation" below). No effect on the other values; rejected if given together with a value that doesn't support it |
 | `--presence-threshold` | `1` | Minimum count for a kmer to be considered present, for `jaccard`/`mash` on a count index |
@@ -30,7 +30,7 @@ Every value routes to one of two independent computations:
 ### Whole-index metrics
 
 | Value | Definition |
-|---|---|
+| --- | --- |
 | `jaccard` | $D = 1 - \dfrac{\lvert A \cap B \rvert}{\lvert A \cup B \rvert}$ over the sets of kmers present in each genome |
 | `mash` | derived from the Jaccard distance via $D = -\dfrac{1}{k} \ln\!\left(\dfrac{2J}{1+J}\right)$ where $J = 1 - D_{\text{jaccard}}$ and $k$ is the index's kmer size; clamped to 1.0 when $J \le 0$ |
 | `hamming` | number of kmer positions where presence differs between the two genomes (presence index only, not normalized): $D = \sum_i \mathbb{1}[a_i \ne b_i]$ |
@@ -112,7 +112,7 @@ Without `-o`, the matrix goes to stdout in relaxed-PHYLIP format (`n` on the fir
 ## `--exclude-genome`, `--min-shared-family`
 
 | Option | Description |
-|---|---|
+| --- | --- |
 | `--exclude-genome LABEL` | Exclude a genome (repeatable). Drops its row/column from the distance/shared-kmer matrix output, and removes it from the sampling used by `--pseudo-alignment`/`--sankoff`/a `snp-*` `--distance` value. Does not change the value computed for any remaining pair |
 | `--min-shared-family N` | Auto-exclude, on top of `--exclude-genome`, any genome whose mean shared-family count against every other genome (see "Family Overlap" below) falls below `N`. Applies only to `--pseudo-alignment`/`--sankoff`/`snp-*` `--distance` — never to the whole-index metrics or their matrix/NJ/UPGMA output |
 
@@ -123,7 +123,7 @@ Neighbor-Joining and UPGMA trees (`--nj`/`--upgma`) are always built from every
 Requires the sibling annex, built once per index:
 
 | Option | Description |
-|---|---|
+| --- | --- |
 | `--sibling-annex` | Build (or rebuild) the sibling-count/minorant annex — prerequisite for every option in this section, and for a `snp-*` `--distance` value |
 | `--sibling-stats` | Write `<prefix>_siblings.csv`: the family-size distribution, per genome and globally |
 | `--sibling-hist` | Print the global family-size histogram (1-4 members) only |
@@ -138,7 +138,7 @@ A family is eligible for a genome pair $(i,j)$ only if both genomes carry exactl
 `<prefix>_siblings.csv` — family size = number of distinct central bases observed at a family (1-4).
 
 | Column | Meaning |
-|---|---|
+| --- | --- |
 | `genome` | genome label, or the literal `global` for the last row |
 | `1`, `2`, `3`, `4` | for a genome row: number of families of that size where the genome carries ≥ 1 member. For the `global` row: the actual deduplicated family-size histogram — not the sum of the rows above |
 
@@ -153,7 +153,7 @@ A family is eligible for a genome pair $(i,j)$ only if both genomes carry exactl
 `<prefix>_alignment.fasta` — one record per non-excluded genome, one column per variable family (family size ≥ 2). Each site is IUPAC-coded from the genome's presence mask at that family: a single observed form → the plain base; several forms → the matching IUPAC ambiguity code; no form → `-`.
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--subsample N` | none (mandatory here) | Target number of families to sample |
 | `--free-loss` | off | Treat a genome carrying none of a family's observed members as missing data (`?`) instead of `-` |
 | `--no-ambiguity` | off | Treat a genome carrying more than one member of a family as missing data (`?`) instead of an IUPAC ambiguity code |
@@ -171,7 +171,7 @@ Every invocation, with or without `--session`, draws its own fresh random sample
 ### `--session`: reusing a sample across separate commands
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--session DIR` | none | Persist the sample (and, for `--sankoff`, its calibration/alignment) in `DIR` so a later, separate `obikmer phylo` invocation with the exact same selection parameters restores it instead of resampling |
 | `--session-force` | off | With `--session DIR`: overwrite its saved parameters and cached sample instead of erroring out when this run's parameters don't match. No effect without `--session` |
 
@@ -188,7 +188,7 @@ Without `--subsample`, every variable family (family size ≥ 2) is used. With `
 `<prefix>_entropy.csv` has one row per family visited:
 
 | Column | Meaning |
-|---|---|
+| --- | --- |
 | `layer` | an internal index-layer identifier — stable within one run, not meaningful across indexes |
 | `family_idx` | the family's position within that layer |
 | `entropy15` | Shannon entropy (bits) over the 16 possible states (the 15 non-empty subsets of `{A,C,G,T}`), genomes absent from the family excluded from the count |
@@ -207,7 +207,7 @@ The first `phylo` run on a given index that uses `--entropy`/`--entropy-sd` pays
 ## Sankoff calibration and phylogenetic exports
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--sankoff` | off | Calibrate a 16-state parsimony cost matrix and matching pseudo-alignment. Requires `--subsample N` |
 | `--sankoff-ratio-ceiling` | `0.5` | Exclude genome pairs whose raw SNP ratio exceeds this value from the base-composition part of the calibration |
 | `--free-loss` | off | Recode a family's non-detection as the `?` missing-data symbol instead of an ordinary, costed state, throughout `--sankoff` and every export built from it |
@@ -242,7 +242,7 @@ With `-o/--output PREFIX`, the relevant subset of the files below is written. Wi
 ### Distance matrix
 
 | File | Written by | Format | Content |
-|---|---|---|---|
+| --- | --- | --- | --- |
 | `<prefix>_dist.phy` | always, unless `--csv` | relaxed PHYLIP | the `--distance` matrix |
 | `<prefix>_dist.csv` | `--csv` | CSV matrix | the `--distance` matrix, 6 decimals |
 | `<prefix>_shared.csv` | `--shared-kmers` | CSV matrix | shared-kmer count per genome pair (integers) |
@@ -254,7 +254,7 @@ CSV matrix layout (`_dist.csv`, `_shared.csv`, `_family_overlap.csv`): header `g
 ### Central-position SNP model
 
 | File | Written by | Format | Content |
-|---|---|---|---|
+| --- | --- | --- | --- |
 | `<prefix>_siblings.csv` | `--sibling-stats` | CSV table | family-size distribution, per genome and global |
 | `<prefix>_family_overlap.csv` | `--family-overlap` | CSV matrix | variable families both genomes of a pair carry a call for |
 | `<prefix>_entropy.csv` | `--shannon` | CSV table | per-family Shannon entropy, see "Sampling at scale" above |
@@ -263,7 +263,7 @@ CSV matrix layout (`_dist.csv`, `_shared.csv`, `_family_overlap.csv`): header `g
 ### Sankoff calibration and exports
 
 | File | Written by | Format | Content |
-|---|---|---|---|
+| --- | --- | --- | --- |
 | `<prefix>_sankoff_matrix.csv` | `--sankoff`/`--tnt`/`--phyg`/`--iqtree` | CSV matrix | calibrated 16×16 cost matrix |
 | `<prefix>_sankoff_params.yaml` | same flags | YAML | calibration report (raw tallies + derived probabilities) |
 | `<prefix>_sankoff.fasta` | same flags | FASTA | Sankoff-recoded pseudo-alignment, header carries an `n_sites` annotation |
@@ -279,7 +279,7 @@ CSV matrix layout (`_dist.csv`, `_shared.csv`, `_family_overlap.csv`): header `g
 **`_sankoff_params.yaml`**:
 
 | Key | Meaning |
-|---|---|
+| --- | --- |
 | `ratio_ceiling` | the `--sankoff-ratio-ceiling` value used |
 | `cardinality_transitions` | 5×5 list of `{from, to, count, probability}`, family cardinality (0-4 observed forms) |
 | `composition_transitions` | 4×4 list of `{from, to, count, probability}`, base letters `A/C/G/T`, single-copy substitutions |
@@ -295,9 +295,8 @@ CSV matrix layout (`_dist.csv`, `_shared.csv`, `_family_overlap.csv`): header `g
 **`_iqtree.model`** (`--iqtree`) — lower-triangular exchangeability matrix $R(a,b) = e^{-\text{cost}(a,b)}$ (one row of increasing length per state, whitespace-separated, PAML order), followed by one line of empirical state frequencies. Only states actually occurring in the alignment are kept, compactly renumbered `0..k-1`.
 
 **`_iqtree.fasta`** (`--iqtree`) — alignment recoded to that same compact `0..k-1` alphabet (symbols `0-9A-F`). Under `--free-loss`, non-detection becomes `?` and columns left non-informative once missing calls are ignored are dropped first (required for `+ASC`); with `--iqtree-min-freq` also set (the default), any state rarer than that threshold is folded into the same `?` treatment, and non-informative columns are re-checked and dropped again. Run with:
-```
-iqtree3 -s <prefix>_iqtree.fasta --seqtype MORPH -m <prefix>_iqtree.model+ASC --prefix <prefix>_iqtree -T AUTO
-```
+
+    iqtree3 -s <prefix>_iqtree.fasta --seqtype MORPH -m <prefix>_iqtree.model+ASC --prefix <prefix>_iqtree -T AUTO
 
 **`_iqtree_states.csv`** (`--iqtree`) — one row per state actually kept in `_iqtree.model`/`_iqtree.fasta` (header `iqtree_symbol,canonical_symbol,frequency`): `iqtree_symbol` is the compact `0-9A-F` symbol as written in those two files, `canonical_symbol` is the matching `_sankoff_matrix.csv` state, `frequency` is that state's empirical frequency at full precision. Under `--free-loss`, absent (`0`/`?`) is never a kept state, so it never appears here — nor does any state `--iqtree-min-freq` folded away for being too rare.
 
diff --git a/usage-predicates.md b/usage-predicates.md
index 17d2a3e..9da5e14 100644
--- a/usage-predicates.md
+++ b/usage-predicates.md
@@ -5,7 +5,7 @@ Several commands ([`filter`](usage-filter), [`select`](usage-select), [`dump`](u
 ## Predicate syntax
 
 | Form | Meaning |
-|---|---|
+| --- | --- |
 | `*` or `all` | Matches every genome (case-insensitive) |
 | `key=v1\|v2` | Genome's `key` metadata equals one of the listed values |
 | `key!=v` | Genome's `key` metadata does not equal `v` |
@@ -20,9 +20,7 @@ Multiple `--ingroup` predicates are combined with AND; multiple `--outgroup` pre
 
 A metadata value is treated as a taxonomy path when it starts with the literal prefix `taxonomy:/`; any other value is treated as a plain string and only supports `=`/`!=`.
 
-```
-taxonomy:/segment1@rank1/segment2@rank2/...
-```
+    taxonomy:/segment1@rank1/segment2@rank2/...
 
 Each segment is a name, optionally annotated with a rank (e.g. `@family`, `@genus`, `@species`); ranks are optional and can be mixed within a path. The `@` character is reserved inside taxonomy paths and cannot appear in segment names or rank labels.
 
@@ -31,7 +29,7 @@ Each segment is a name, optionally annotated with a rank (e.g. `@family`, `@genu
 Matching compares segment names only (ranks are informational, not part of the match), with anchoring controlled by leading/trailing `/`:
 
 | Pattern | Matches |
-|---|---|
+| --- | --- |
 | `A/B` | anywhere in the path |
 | `/A/B` | at the start of the path (prefix) |
 | `A/B$` | at the end of the path (suffix) |
diff --git a/usage-query.md b/usage-query.md
index 01fea10..1c1a456 100644
--- a/usage-query.md
+++ b/usage-query.md
@@ -9,14 +9,14 @@ obikmer query INDEX INPUTS... [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory to query against |
 | `INPUTS...` | Input sequence files (FASTA/FASTQ, gzip optional); at least one required |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--detail` | off | Report per-position, per-genome coverage vectors in the output |
 | `--count-missing` | off | Also count query kmers absent from the index |
 | `--force-presence` | off | Report presence (0/1) per genome instead of raw counts |
diff --git a/usage-select.md b/usage-select.md
index 401aa9a..38fe11b 100644
--- a/usage-select.md
+++ b/usage-select.md
@@ -9,13 +9,13 @@ obikmer select SOURCE --output OUTPUT [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `SOURCE` | Source index directory |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
+| --- | --- | --- |
 | `-o, --output` | — | Output index directory (required) |
 | `-f, --force` | off | Overwrite an existing output directory |
 | `--group NAME:PRED` | none | Define a named group of genomes by predicate (repeatable; mutually exclusive with `--aggregate-by`) |
diff --git a/usage-superkmer.md b/usage-superkmer.md
index eafacbd..53195ca 100644
--- a/usage-superkmer.md
+++ b/usage-superkmer.md
@@ -9,14 +9,14 @@ obikmer superkmer [OPTIONS] [INPUTS...]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INPUTS...` | Input sequence files or directories (FASTA/FASTQ/GenBank, gzip optional). If omitted, reads from stdin. |
 
 ## Options
 
 | Option | Default | Description |
-|---|---|---|
-| `-k, --kmer-size` | `31` | Kmer size (must be odd, in [11, 31]) |
+| --- | --- | --- |
+| `-k, --kmer-size` | `31` | Kmer size (must be odd, in \[11, 31\]) |
 | `-m, --minimizer-size` | `11` | Minimizer size (must be odd, in $[3, k-1]$) |
 | `--theta` | `0.7` | Entropy threshold; kmers with a normalized entropy at or below this value are excluded |
 | `--level-max` | `6` | Maximum sub-word size used for the entropy score |
diff --git a/usage-unitig.md b/usage-unitig.md
index a126d0e..0118dff 100644
--- a/usage-unitig.md
+++ b/usage-unitig.md
@@ -9,7 +9,7 @@ obikmer unitig INDEX [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEX` | Index directory |
 
 ## Options
diff --git a/usage-utils.md b/usage-utils.md
index 38654c8..293293b 100644
--- a/usage-utils.md
+++ b/usage-utils.md
@@ -9,13 +9,13 @@ obikmer utils INDEXES... [OPTIONS]
 ## Arguments
 
 | Argument | Description |
-|---|---|
+| --- | --- |
 | `INDEXES...` | One or more index directories |
 
 ## Options
 
 | Option | Scope | Description |
-|---|---|---|
+| --- | --- | --- |
 | `--new-label NEW=OLD` | single index only | Rename a genome label |
 | `--upgrade-index` | single index only | Add any missing layer metadata files to an older index |
 | `--bits-per-kmer` | single index only | Print bits-per-kmer statistics |