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1.
Nucleic Acids Res ; 51(D1): D1188-D1195, 2023 01 06.
Artículo en Inglés | MEDLINE | ID: mdl-36420891

RESUMEN

The UCSC Genome Browser (https://genome.ucsc.edu) is an omics data consolidator, graphical viewer, and general bioinformatics resource that continues to serve the community as it enters its 23rd year. This year has seen an emphasis in clinical data, with new tracks and an expanded Recommended Track Sets feature on hg38 as well as the addition of a single cell track group. SARS-CoV-2 continues to remain a focus, with regular annotation updates to the browser and continued curation of our phylogenetic sequence placing tool, hgPhyloPlace, whose tree has now reached over 12M sequences. Our GenArk resource has also grown, offering over 2500 hubs and a system for users to request any absent assemblies. We have expanded our bigBarChart display type and created new ways to visualize data via bigRmsk and dynseq display. Displaying custom annotations is now easier due to our chromAlias system which eliminates the requirement for renaming sequence names to the UCSC standard. Users involved in data generation may also be interested in our new tools and trackDb settings which facilitate the creation and display of their custom annotations.


Asunto(s)
Bases de Datos Genéticas , Genómica , Humanos , COVID-19/epidemiología , COVID-19/genética , Genómica/métodos , Internet , Filogenia , SARS-CoV-2/genética , Programas Informáticos , Navegador Web
2.
Nucleic Acids Res ; 50(D1): D1115-D1122, 2022 01 07.
Artículo en Inglés | MEDLINE | ID: mdl-34718705

RESUMEN

The UCSC Genome Browser, https://genome.ucsc.edu, is a graphical viewer for exploring genome annotations. The website provides integrated tools for visualizing, comparing, analyzing, and sharing both publicly available and user-generated genomic datasets. Data highlights this year include a collection of easily accessible public hub assemblies on new organisms, now featuring BLAT alignment and PCR capabilities, and new and updated clinical tracks (gnomAD, DECIPHER, CADD, REVEL). We introduced a new Track Sets feature and enhanced variant displays to aid in the interpretation of clinical data. We also added a tool to rapidly place new SARS-CoV-2 genomes in a global phylogenetic tree enabling researchers to view the context of emerging mutations in our SARS-CoV-2 Genome Browser. Other new software focuses on usability features, including more informative mouseover displays and new fonts.


Asunto(s)
Bases de Datos Genéticas , Navegador Web , Animales , Genoma Humano , Humanos , Filogenia , Reacción en Cadena de la Polimerasa , SARS-CoV-2/genética , Interfaz Usuario-Computador , Secuenciación del Exoma
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