383da828477aad2b3c6053880a64fdbfc2a00cd9 max Thu Mar 19 02:30:41 2026 -0700 Fix varFreqs HTML issues and trexplorer citation, from AI code review 2026-03-19, refs #36642 Fix broken $db download URLs to hg38 in 14 HTML files, correct "Japanese" to "Korean" in kova.html, fix "area" typo in schema.html, fix "Finnland" to "Finland" in varFreqs.ra, normalize GREGoR capitalization, fix grammar, quote all target=_blank attributes, capitalize GitHub consistently, and fix bioRxiv citation formatting in trexplorer.html. Co-Authored-By: Claude Opus 4.6 <noreply@anthropic.com> diff --git src/hg/makeDb/trackDb/human/npm.html src/hg/makeDb/trackDb/human/npm.html index 276ff733c10..d404811c7c5 100644 --- src/hg/makeDb/trackDb/human/npm.html +++ src/hg/makeDb/trackDb/human/npm.html @@ -20,32 +20,32 @@ <h2>Methods</h2> <p> Whole Genome Sequencing (WGS) data processing followed GATK4 best practices. GATK4 germline variant analysis workflow written in WDL was adapted to use Nextflow and deployed at the National Supercomputing Centre, Singapore (NSCC). WGS reads were aligned against GRCh38 using the BWA-MEM algorithm and used as input to GATK HaplotypeCaller to produce single sample gVCFs. The gVCF files were joint-called then loaded in Hail. Low-quality WGS libraries and low-quality variants were removed. QC-ed variants were functionally annotated using Ensembl Variant Effect Predictor (VEP) (version 95). Functional annotations for variants impacting protein-coding regions were also complemented with information on the potential alteration to their cognate protein's 3D structure and drug binding ability. </p> <p> Our data access request was approved by the NPM data access committee. It can be contacted at contact_npco@a-star.edu.sg. We downloaded the data from the NPM Chorus browser download section. -We provide documentation that indicates how all source files of the varFreqs track were converted in the <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/hg38/varFreqs.txt" target=_blank>makeDoc file</a> of the track. -For some tracks, python scripts were necessary and are also available from <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/scripts/varFreqs" target=_blank>Github</a>. +We provide documentation that indicates how all source files of the varFreqs track were converted in the <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/doc/hg38/varFreqs.txt" target="_blank">makeDoc file</a> of the track. +For some tracks, python scripts were necessary and are also available from <a href="https://github.com/ucscGenomeBrowser/kent/blob/master/src/hg/makeDb/scripts/varFreqs" target="_blank">GitHub</a>. </p> <h2>Credits</h2> <p> Thanks to the NPM Data Access Committee and Eleanor for granting our data request. By browsing the data, you agree to use the data only for academic, non-commercial research to improve human health (biology/disease). We request all data users agree to protect the confidentiality of the data subjects in any research papers or publications that they may prepare, by taking all reasonable care to limit the possibility of identification. In particular, the data users shall not use, or attempt to use, the data to deliberately compromise or otherwise infringe the confidentiality of information on data subjects and their right to privacy. If you use any of the data obtained from the CHORUS variant browser, we request that you cite the NPM flagship paper (Wong et al, 2023). All data users of the data must take note that the data provider and relevant SG10K_Health cohort