UCSC Genome Browser @GenomeBrowser
The UCSC Genome Browser is a public, freely available, open-source web-based graphical viewer for the display of genome sequences and their annotations. genome.ucsc.edu Santa Cruz, CA, USA Joined May 2011-
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Exploring Transcription factor Binding with UCSC Genome Browser youtube.com/watch?v=gguXc8…
We are excited to announce the release of the AbSplice scores track that was previously only on hg38 and is now also available on hg19. The scores represent the probability that a given variant causes aberrant splicing in a given tissue. More info at bit.ly/AbSpliceScores…
The Genome Browser is experiencing issues and our system administrators are working to bring the site back as soon as possible. Please use one of these UCSC Genome Browser mirror servers in the meantime: Europe mirror: genome-euro.ucsc.edu Asia mirror: genome-asia.ucsc.edu
We are pleased to announce the release of the gnomAD (@gnomad_project) v4 constraint metrics for hg38 and the addition of a non-cancer filter for the hg19 Exome Variants v2.1.1 and the hg38 Genome Variants v3.1.1 tracks. Learn more at bit.ly/gnomAD_032624
We are happy to announce the new Human Prediction Scores super track for the GRCh37/hg19 assembly. This super track currently includes the BayesDel track, which can be used for clinical variant classification research. More information is available at bit.ly/BayesDel
We are excited to announce the new JASPAR 2024 tracks for hg19, hg38, mm10, and mm39 which represent genome-wide predicted binding sites for transcription factors with binding profiles in the JASPAR CORE collection (@jaspar_db). Learn more at bit.ly/JASPAR2024
We are happy to announce the release of the AbSplice scores track for the human genome, GRCh38/hg38. The scores represent the probability that a given variant causes aberrant splicing in a given tissue. Learn more at: genome.ucsc.edu/goldenPath/new…
DECIPHER has a new handle! To better reflect our URL and to make it easier to find us, we are now @deciphergenonomic
We are happy to announce the release of the All GENCODE tracks for hg19, hg38, and mm39. These tracks correspond with the @ensembl 111 release. Learn more about the release from the following news post: bit.ly/4bDSxj3
We are happy to announce an update to the Variants of Concern track to include the latest WHO-designated variants of concern (VOC) for the SARS-CoV-2 genome. Learn more about this release at: genome.ucsc.edu/goldenPath/new…
The CRISPR Targets track is now available for human (T2T CHM13v2.0). The CRISPR Targets track shows the DNA sequences targetable by CRISPR RNA guides using the Cas9 enzyme from S. pyogenes (PAM: NGG) over the entire human genome. Learn more at: tinyurl.com/3ce6jxea
Quick update, all services should be back online. The only exceptions are some BLAT servers that are still coming back slowly, notably hg19. It should be back in the next hour or so. Thank you all for your patience while we addressed the situation.
Most of our resources are back online. The last few items will be out BLAT and isPCR servers. Those are being restarted and the full process will take a few hours.
We are currently getting some severe weather in Santa Cruz, CA. It is affecting many of our systems, and parts of our site are down. Our euro mirror (genome-euro.ucsc.edu) is mostly functioning. We apologize for the inconvenience and hope to be back online soon.
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Excited to share with the single-cell community the most recent work of @tmontsay and @AEsteveCodina from @cnag_eu, something we think will be a game-changer in #scRNAseq quality control: biorxiv.org/content/10.110… @biorxivpreprint Get ready for the tweetorial! 1/10
Awe, shucks. So nice to get good feedback from wonderful colleagues!
@christinerbeck: crystal clear talk on TE-mediated structural variation in human genomes. Exploit long read data to find previously hidden variants and study allelic heterogeneity within polymorphic insertions. Long reads are such a game changer in our field! #icte2024
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Farewell to Guernsey and on to St Malo for #ICTE2024. Lovely day in this corner of the Atlantic
✨ Delighted to introduce Dr. Silvie Fexova, our exceptional Data Submissions Lead. Since her arrival in 2018, Silvie has played a pivotal role in our data success journey, demonstrating unmatched expertise and dedication in every submission #MeetTheTeam #internationalwomensday
DECIPHER has a new handle! To better reflect our URL and to make it easier to find us, we are now @deciphergenonomic
DNA language models are powerful predictors of genome-wide variant effects biorxiv.org/content/10.110… UCSC: genome.ucsc.edu/s/gbenegas/gpn… Code: github.com/songlab-cal/gpn
New release of UCSC Genome Browser: the Problematic Regions tracks for hg38. @GenomeBrowser genome.ucsc.edu/goldenPath/new…
I’m delighted to announce major performance improvements to the UShER web interface usher.bio, thanks to the incredible work of Cheng Ye, @yatishturakhia’s student, and the rest of team UShER. A handful of sequences → subtree views in ~1min instead of ~5min.
Sawasdee 🙏! The UCSC Team is here at the #HCA2022Asia meeting in Bangkok! Come check out our posters tomorrow Nov 4th at posters #25 and #26. #SingleCell #visualization @humancellatlas
@GenomeBrowser @hrhotz @PanelApp @genenames I think that should be: @PanelAppTeam
@GenomeBrowser @PanelApp Great to see HGNC (inc. HGNC ID) and @PanelAppTeam tracks in the Genome browser. Great work!
A walk to view the beautiful California coast scheduled into the meeting? I approve! #UCSC Genomics Institute. @GenomeBrowser SAB!
Please use this data! Use it to learn about patterns of miRNA expression, to review miRNA papers, to generate hypotheses, etc, etc. All the data is available in the paper, in an R package and at the @GenomeBrowser.
@GenomeBrowser This looks great thanks for putting it together!
👋 #veptc2022 starts Tues! There is still⌛️to join! Check out the program 👀 veptc.variome.org Workshops ✅ @ACMG recs✅ @GenomeBrowser✅ @ensembl✅ HGVS Nomenclature ✅ NGS in diagnostics ✅ Mitochondrial Dx by WES✅ LR Seq ✅ HPO ✅ Funct Testn ✅ #Genomics #Genetics