38ccb38771eddfec3230ab3494fb12e11e7cb4ac
jnavarr5
  Fri Sep 25 17:52:32 2026 -0700
Putting references in alphabetical order. Adding years to citations. Not using the word 'here' and using the actual location/noun. refs #35528

diff --git src/hg/makeDb/trackDb/human/proCapNet.html src/hg/makeDb/trackDb/human/proCapNet.html
index 6ea55a46079..6f90f9f7db8 100644
--- src/hg/makeDb/trackDb/human/proCapNet.html
+++ src/hg/makeDb/trackDb/human/proCapNet.html
@@ -83,56 +83,56 @@
 
 <h3>Model</h3>
 
 <p>
 ProCapNet adapts the BPNet architecture. It reads 2,114 bp of one-hot encoded
 sequence and outputs both a base-resolution profile over the central 1,000 bp,
 covering both strands as a single softmax so the model can learn strand
 asymmetry, and a scalar giving the log total number of initiation events in that
 window. Training used ENCODE PRO-cap read alignments in which the first read of
 each pair was discarded and only the single 5'-most base of the second read was
 kept, merged across replicates and kept separate by strand. Each model was
 trained on all PRO-cap peaks in its cell line plus randomly sampled
 DNase-hypersensitive sites from the same cell line at a 7:1 peak to background
 ratio, with 7-fold cross-validation split by chromosome. Bases that are not
 uniquely mappable by 36-mer reads were given zero loss weight during training.
-Full details are in Cochran <em>et al</em>.
+Full details are in Cochran <em>et al.</em>, 2024.
 </p>
 
 <h3>Predicted PRO-cap</h3>
 
 <p>
 Genome-wide predictions were generated by the Kundaje lab by applying the model
 to every 2,114 bp window at a stride of 250 bp, so each base is the average of
 four overlapping predictions, then averaging across the seven cross-validation
 models and across the forward and reverse-complemented sequence. On hg38 no
 prediction was made where most of a window was unresolved (N) in the reference.
 </p>
 
 <h3>Sequence contribution scores</h3>
 
 <p>
 Scores were computed with DeepSHAP, which estimates each base's contribution by
 contrasting the model's output on the real sequence against its output on a set
 of reference sequences, here 25 dinucleotide shuffles of the sequence being
 scored. Because DeepSHAP needs a single scalar to explain, the base-resolution
 profile output was summarized by mean-normalizing the pre-softmax logits and
 taking their dot product with the post-softmax profile, which weights each
 base's logit by its predicted probability of being used and sums over the
 1,000 bp output window and both strands. This is the profile or TSS-positioning
 task; ProCapNet can also produce scores for its read-count task, which are not
-shown here. Each scored sequence was run through all seven cross-validation
+included in this track. Each scored sequence was run through all seven cross-validation
 models and in both orientations, and the scores averaged.
 </p>
 
 <h3>Source</h3>
 
 <p>
 The ProCapNet model implementation is at
 <a href="https://github.com/kundajelab/ProCapNet" target="_blank">kundajelab/ProCapNet</a>.
 The steps that turned the published files into these tracks are recorded in
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/$db/transcriptionStart.txt"
 target="_blank">doc/$db/transcriptionStart.txt</a>, the scripts they run are in
 <a href="https://github.com/ucscGenomeBrowser/kent/tree/master/src/hg/makeDb/outside/proCapNet"
 target="_blank">makeDb/outside/proCapNet</a>, and the track configuration is in
 <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/trackDb/human/$db/transcriptionStart.ra"
 target="_blank">trackDb/human/$db/transcriptionStart.ra</a>.
@@ -154,80 +154,75 @@
 The Files column of the table on this page links each cell line's bigWigs
 directly, so a single file can be fetched without working out its path.
 </p>
 
 <p>
 For automated download and analysis, the genome annotation is stored in bigWig
 files that can be downloaded from
 <a href="http://hgdownload.soe.ucsc.edu/gbdb/$db/proCapNet/" target="_blank">our
 download server</a>. Predictions are under <tt>pred/</tt> and are named for the
 cell line, the model and the strand, for example
 <tt>K562.proCapNet.pos.bw</tt> and <tt>K562.proCapNet.neg.bw</tt>. Contribution
 scores, which exist for GRCh38 only, are under <tt>contrib/</tt>, for example
 <tt>K562.proCapNet-contrib.bw</tt>. Individual regions or the whole genome annotation
 can be obtained using our tool <tt>bigWigToBedGraph</tt>, which can be compiled
 from the source code or downloaded as a precompiled binary for your system.
-Instructions for downloading source code and binaries can be found
-<a href="http://hgdownload.soe.ucsc.edu/downloads.html#utilities_downloads" target="_blank">here</a>.
+Instructions for downloading source code and binaries are on the
+<a href="http://hgdownload.soe.ucsc.edu/downloads.html#utilities_downloads"
+target="_blank">utilities download page</a>.
 The tool can also be used to obtain features within a given range, e.g.
 <tt>bigWigToBedGraph http://hgdownload.soe.ucsc.edu/gbdb/$db/proCapNet/pred/K562.proCapNet.pos.bw
 -chrom=chr21 -start=0 -end=100000000 stdout</tt>
 </p>
 
 <p>
 The ProCapNet models are on the
 <a href="https://www.encodeproject.org" target="_blank">ENCODE portal</a> as
 BPNet-model annotations, one per cell line, linked from the Experiment column of
 the table on this page. Each annotation also holds the trained model, sequence
 contribution scores and predicted signal over a selected set of regions. The
 genome-wide predictions shown here are not part of that ENCODE release.
 </p>
 
 <h2>Credits</h2>
 
 <p>
 ProCapNet was developed by Kelly Cochran in the Kundaje lab at Stanford
 University. The genome-wide predictions and contribution scores were generated by
 Kelly Cochran in collaboration with the GENCODE consortium. Thanks to Kelly
 Cochran and Anshul Kundaje for making the data available.
 </p>
 
 <h2>References</h2>
 
-
-<p>
-Cochran K, Yin M, Mantripragada A, Schreiber J, Marinov GK, Shah SR, Yu H, Lis JT, Kundaje A.
-<a href="https://www.ncbi.nlm.nih.gov/pubmed/38853896" target="_blank">
-Dissecting the cis-regulatory syntax of transcription initiation with deep learning</a>.
-<em>bioRxiv</em>. 2024 Nov 21;.
-DOI: <a href="https://doi.org/10.1101/2024.05.28.596138"
-target="_blank">10.1101/2024.05.28.596138</a>; PMID: <a
-href="https://www.ncbi.nlm.nih.gov/pubmed/38853896" target="_blank">38853896</a>; PMC: <a
-href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11160661/" target="_blank">PMC11160661</a>
-</p>
-
-
-
 <p>
 Avsec &#381;, Weilert M, Shrikumar A, Krueger S, Alexandari A, Dalal K, Fropf R, McAnany C, Gagneur J,
 Kundaje A <em>et al</em>.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/33603233" target="_blank">
 Base-resolution models of transcription-factor binding reveal soft motif syntax</a>.
 <em>Nat Genet</em>. 2021 Mar;53(3):354-366.
 DOI: <a href="https://doi.org/10.1038/s41588-021-00782-6"
 target="_blank">10.1038/s41588-021-00782-6</a>; PMID: <a
 href="https://www.ncbi.nlm.nih.gov/pubmed/33603233" target="_blank">33603233</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8812996/" target="_blank">PMC8812996</a>
 </p>
 
-
+<p>
+Cochran K, Yin M, Mantripragada A, Schreiber J, Marinov GK, Shah SR, Yu H, Lis JT, Kundaje A.
+<a href="https://www.ncbi.nlm.nih.gov/pubmed/38853896" target="_blank">
+Dissecting the cis-regulatory syntax of transcription initiation with deep learning</a>.
+<em>bioRxiv</em>. 2024 Nov 21;.
+DOI: <a href="https://doi.org/10.1101/2024.05.28.596138"
+target="_blank">10.1101/2024.05.28.596138</a>; PMID: <a
+href="https://www.ncbi.nlm.nih.gov/pubmed/38853896" target="_blank">38853896</a>; PMC: <a
+href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11160661/" target="_blank">PMC11160661</a>
+</p>
 
 <p>
 Kwak H, Fuda NJ, Core LJ, Lis JT.
 <a href="https://www.ncbi.nlm.nih.gov/pubmed/23430654" target="_blank">
 Precise maps of RNA polymerase reveal how promoters direct initiation and pausing</a>.
 <em>Science</em>. 2013 Feb 22;339(6122):950-3.
 DOI: <a href="https://doi.org/10.1126/science.1229386" target="_blank">10.1126/science.1229386</a>;
 PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/23430654" target="_blank">23430654</a>; PMC: <a
 href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974810/" target="_blank">PMC3974810</a>
 </p>
-