7072384d5e6f4228bec4186d3d677527be0c9bc5 mspeir Fri Jun 26 09:37:20 2026 -0700 Adding data access to hs1 pages on the RR, refs # diff --git src/hg/makeDb/trackDb/human/hs1/html/hgUnique.html src/hg/makeDb/trackDb/human/hs1/html/hgUnique.html index 16ba2b6495d..33b7a16e744 100644 --- src/hg/makeDb/trackDb/human/hs1/html/hgUnique.html +++ src/hg/makeDb/trackDb/human/hs1/html/hgUnique.html @@ -1,45 +1,69 @@
These tracks show the regions unique to the T2T-CHM13 v2.0 assembly compared to the GRCh38/hg38 and GRCh37/hg19 reference assemblies.
We used the `to_paf.py` script from chaintools (https://doi.org/10.5281/zenodo.6342391, v0.1) to convert the v1_nfLO chains to the PAF format.
We used the follwing commands to obtain the regions unique to GRCh38/hg38 and GRCh37/hg19 in the BED format.
cut -f 1,3,4 grch38-chm13v2.paf \
| bedtools sort -i - -g chm13v2.0.fasta.fai \
| bedtools merge \
| bedtools complement -g chm13v2.0.fasta.fai -i - \
| bedtools merge \
> T2T-CHM13v2.0_unique_regions_hg38.bed
cut -f 1,3,4 hg19-chm13v2.paf | bedtools sort -i - -g chm13v2.0.fasta.fai \
| bedtools merge \
| bedtools complement -g chm13v2.0.fasta.fai -i - \
| bedtools merge \
> T2T-CHM13v2.0_unique__regions_hg19.bed
++The raw data can be explored interactively with the +Table Browser or the +Data Integrator. The data can also be +accessed from scripts through our REST +API.
++This track is a container of multiple subtracks; the underlying data are stored in bigBed files +that can be downloaded from our +download server. +Individual regions or the whole genome annotation can be obtained using our tool +bigBedToBed, 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 +here. +The tool can also be used to obtain only features within a given range, for example:
+bigBedToBed https://hgdownload.soe.ucsc.edu/gbdb/$db/hgUnique/hgUnique.hg38.bb -chrom=chr6 -start=0 -end=1000000 stdout ++Please refer to our +mailing +list archives for questions, or our +Data Access FAQ for more +information.
+The unique region annotations were generated by Nae-Chyun Chen<naechyun.chen@gmail.com> and Mitchell Vollger<mvollger@uw.edu>
Nurk S, Koren S, Rhie A, Rautiainen M, et al. The complete sequence of a human genome. bioRxiv, 2021.