diff --git a/.github/workflows/cd.yaml b/.github/workflows/cd.yaml
index 7c65d7abd..e2d99494f 100644
--- a/.github/workflows/cd.yaml
+++ b/.github/workflows/cd.yaml
@@ -4,6 +4,7 @@ on:
   push:
     branches:
       - main
+      - staging/sprocket-doc
 
 jobs:
   gh-pages:
@@ -17,11 +18,11 @@ jobs:
         run: rustup update stable && rustup default stable
       - name: Build Sprocket
         run: |
-          cargo install sprocket --locked
+          cargo install sprocket --locked --git https://github.com/Serial-ATA/sprocket.git --branch doc-tables
       - name: Build Docs
         run: |
           cd $GITHUB_WORKSPACE/workflows
-          sprocket dev doc -v --homepage assets/DOCS.md --prioritize-workflows-view .
+          sprocket dev doc --homepage assets/DOCS.md --with-doc-comments .
           cp -r assets docs/
       - name: Deploy
         uses: peaceiris/actions-gh-pages@v4
diff --git a/data_structures/flag_filter.wdl b/data_structures/flag_filter.wdl
index 3f1f0826e..c6b97cbf1 100644
--- a/data_structures/flag_filter.wdl
+++ b/data_structures/flag_filter.wdl
@@ -1,6 +1,7 @@
-## # FlagFilter
-##
+version 1.1
+
 ## A struct to represent the filtering flags used in various `samtools` commands.
+##
 ## The order of precedence is `include_if_all`, `exclude_if_any`, `include_if_any`,
 ## and `exclude_if_all`.
 ## These four fields correspond to the samtools flags
@@ -58,14 +59,15 @@
 ## In short, those are all flags corresponding to the quality of the read
 ## and them being `true` may indicate that the read is of low quality and
 ## should be excluded.
-
-version 1.1
-
 struct FlagFilter {
-    String include_if_all  # samtools -f
-    String exclude_if_any  # samtools -F
-    String include_if_any  # samtools --rf
-    String exclude_if_all  # samtools -G
+    ## Corresponds to `samtools -f`
+    String include_if_all
+    ## Corresponds to `samtools -F`
+    String exclude_if_any
+    ## Corresponds to `samtools --rf`
+    String include_if_any
+    ## Corresponds to `samtools -G`
+    String exclude_if_all
 }
 
 task validate_string_is_12bit_int {
diff --git a/data_structures/read_group.wdl b/data_structures/read_group.wdl
index eadb9edc1..91a28a8da 100644
--- a/data_structures/read_group.wdl
+++ b/data_structures/read_group.wdl
@@ -1,32 +1,7 @@
-## Read groups are defined in the SAM spec
-## - `ID`: Read group identifier. Each Read Group must have a unique ID.
-##     The value of ID is used in the RG tags of alignment records.
-## - `BC`: Barcode sequence identifying the sample or library. This value is the
-##     expected barcode bases as read by the sequencing machine in the absence
-##     of errors. If there are several barcodes for the sample/library
-##     (e.g., one on each end of the template), the recommended implementation
-##     concatenates all the barcodes separating them with hyphens (`-`).
-## - `CN`: Name of sequencing center producing the read.
-## - `DS`: Description.
-## - `DT`: Date the run was produced (ISO8601 date or date/time).
-## - `FO`: Flow order. The array of nucleotide bases that correspond to the nucleotides
-##     used for each flow of each read. Multi-base flows are encoded in IUPAC format,
-##     and non-nucleotide flows by various other characters.
-##     Format: `/\\*|[ACMGRSVTWYHKDBN]+/`
-## - `KS`: The array of nucleotide bases that correspond to the key sequence of each read.
-## - `LB`: Library.
-## - `PG`: Programs used for processing the read group.
-## - `PI`: Predicted median insert size, rounded to the nearest integer.
-## - `PL`: Platform/technology used to produce the reads.
-##     Valid values: CAPILLARY, DNBSEQ (MGI/BGI), ELEMENT, HELICOS, ILLUMINA, IONTORRENT,
-##     LS454, ONT (Oxford Nanopore), PACBIO (Pacific Biosciences), SINGULAR, SOLID,
-##     and ULTIMA. This field should be omitted when the technology is not in this list
-##     (though the PM field may still be present in this case) or is unknown.
-## - `PM`: Platform model. Free-form text providing further details of the
-##     platform/technology used.
-## - `PU`: Platform unit (e.g., flowcell-barcode.lane for Illumina or slide
-##     for SOLiD). Unique identifier.
-## - `SM`: Sample. Use pool name where a pool is being sequenced.
+version 1.1
+
+## Read groups are defined in the SAM specification. This struct
+## provides utlity for constructing, validating, and parsing read groups.
 ##
 ## An example input JSON entry for `read_group` might look like this:
 ## ```json
@@ -40,25 +15,50 @@
 ##     }
 ## }
 ## ```
-
-version 1.1
-
 #@ except: SnakeCase
 struct ReadGroup {
+    ## `ID`: Read group identifier. Each Read Group must have a unique ID.
+    ## The value of ID is used in the RG tags of alignment records.
     String ID
-    String? BC
+    ## `CN`: Name of sequencing center producing the read.
     String? CN
+    ## `DS`: Description.
     String? DS
+    ## `DT`: Date the run was produced (ISO8601 date or date/time).
     String? DT
+    ## `FO`: Flow order. The array of nucleotide bases that correspond to the nucleotides
+    ## used for each flow of each read. Multi-base flows are encoded in IUPAC format,
+    ## and non-nucleotide flows by various other characters.
+    ## Format: `/\\*|[ACMGRSVTWYHKDBN]+/`
     String? FO
+    ## `KS`: The array of nucleotide bases that correspond to the key sequence of each read.
     String? KS
+    ## `LB`: Library.
     String? LB
+    ## `PG`: Programs used for processing the read group.
     String? PG
+    ## `PI`: Predicted median insert size, rounded to the nearest integer.
     Int? PI
+    ## `PL`: Platform/technology used to produce the reads.
+    ## Valid values: CAPILLARY, DNBSEQ (MGI/BGI), ELEMENT, HELICOS, ILLUMINA, IONTORRENT,
+    ## LS454, ONT (Oxford Nanopore), PACBIO (Pacific Biosciences), SINGULAR, SOLID,
+    ## and ULTIMA. This field should be omitted when the technology is not in this list
+    ## (though the PM field may still be present in this case) or is unknown.
     String? PL
+    ## `PM`: Platform model. Free-form text providing further details of the
+    ## platform/technology used.
     String? PM
+    ## `PU`: Platform unit (e.g., flowcell-barcode.lane for Illumina or slide
+    ## for SOLiD). Unique identifier.
     String? PU
+    ## `SM`: Sample. Use pool name where a pool is being sequenced.
     String? SM
+    ## `BC`: Barcode sequence identifying the sample or library. This value is the
+    ## expected barcode bases as read by the sequencing machine in the absence
+    ## of errors. If there are several barcodes for the sample/library
+    ## (e.g., one on each end of the template), the recommended implementation
+    ## concatenates all the barcodes separating them with hyphens (`-`).
+    String? BC
 }
 
 workflow read_group_to_string {
diff --git a/data_structures/strandedness.wdl b/data_structures/strandedness.wdl
new file mode 100644
index 000000000..fccfe9a73
--- /dev/null
+++ b/data_structures/strandedness.wdl
@@ -0,0 +1,16 @@
+version 1.3
+
+## Possible strandedness protocols used during RNA-Seq library prep.
+enum Strandedness {
+    ## The protocol is unknown or otherwise unspecified.
+    ##
+    ## Some tooling can automatically derive a suspected strandedness protocol,
+    ## if one is not specified.
+    Unspecified,
+    ## The RNA-Seq library was prepped with an unstranded protocol.
+    Unstranded,
+    ## The RNA-Seq library was prepped with a Stranded-Reverse protocol.
+    StrandedReverse,
+    ## The RNA-Seq library was prepped with a Stranded-Forward protocol.
+    StrandedForward,
+}