-
Notifications
You must be signed in to change notification settings - Fork 3
Commit
This commit does not belong to any branch on this repository, and may belong to a fork outside of the repository.
- Loading branch information
Showing
2 changed files
with
21 additions
and
0 deletions.
There are no files selected for viewing
Loading
Sorry, something went wrong. Reload?
Sorry, we cannot display this file.
Sorry, this file is invalid so it cannot be displayed.
This file contains bidirectional Unicode text that may be interpreted or compiled differently than what appears below. To review, open the file in an editor that reveals hidden Unicode characters.
Learn more about bidirectional Unicode characters
Original file line number | Diff line number | Diff line change |
---|---|---|
@@ -0,0 +1,21 @@ | ||
--- | ||
title: "cancercelllines.org - a Novel Resource for Genomic Variants in Cancer Cell Lines" | ||
description: DATABASE Article | ||
template: post.html | ||
authors: | ||
- '@rahelp' | ||
- '@mbaudis' | ||
date: 2024-03-27 | ||
pdf_file_name: 2024-03-27___Paloots-and-Baudis__cancercelllines.org—a-novel-resource-for-genomic-variants-in-cancer-cell-lines__DATABASE.pdf | ||
links: | ||
- '[preprint at bioarXiv](https://doi.org/10.1101/2023.12.12.571281)' | ||
--- | ||
|
||
#### Rahel Paloots and Michael Baudis | ||
##### Database (Oxford). 2024 Apr 30:2024:baae030. [doi: 10.1093/database/baae030](https://doi.org/10.1093/database/baae030) | ||
##### bioarXiv preprint (2023-12-13): [https://doi.org/10.1101/2023.12.12.571281](https://doi.org/10.1101/2023.12.12.571281) | ||
|
||
![DATABASE logo](/img/logo-database-journal-300x150.png){: style="float: right; width: 150px; margin-top: -100px;"} | ||
**Abstract**: Cancer cell lines are an important component in biological and medical research, enabling studies of cellular mechanisms as well as the development and testing of pharmaceuticals. Genomic alterations in cancer cell lines are widely studied as models for oncogenetic events and are represented in a wide range of primary resources. We have created a comprehensive, curated knowledge resource - cancercelllines.org - with the aim to enable easy access to genomic profiling data in cancer cell lines, curated from a variety of resources and integrating both copy number and single nucleotide variants (SNVs) data. We have gathered over 5,600 copy number profiles as well as SNV annotations for 16,000 cell lines and provide this data with mappings to the GRCh38 reference genome. Both genomic variations and associated curated metadata can be queried through the GA4GH Beacon v2 API and a graphical user interface with extensive data retrieval enabled using GA4GH data schemas under a permissive licensing scheme. | ||
|
||
**Availability and Implementation**: Our resource is publicly available on the web at <https://cancercelllines.org>. |