picklesv2
Code used for updated version of PICKLES (https://doi.org/10.1093/nar/gkx993). Application found at: https://hartlab.shinyapps.io/pickles/
Science Score: 44.0%
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✓CITATION.cff file
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✓codemeta.json file
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○.zenodo.json file
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✓DOI references
Found 2 DOI reference(s) in README -
○Academic publication links
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○JOSS paper metadata
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○Scientific vocabulary similarity
Low similarity (3.2%) to scientific vocabulary
Last synced: 10 months ago
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Repository
Code used for updated version of PICKLES (https://doi.org/10.1093/nar/gkx993). Application found at: https://hartlab.shinyapps.io/pickles/
Basic Info
- Host: GitHub
- Owner: franklenoir
- Language: R
- Default Branch: master
- Size: 3.65 MB
Statistics
- Stars: 0
- Watchers: 1
- Forks: 0
- Open Issues: 0
- Releases: 0
Created over 6 years ago
· Last pushed over 6 years ago
Metadata Files
Readme
Citation
README.md
pickles
PICKLES: web visualization for CRISPR screens
Git repo only contains code used for rshiny database: https://hartlab.shinyapps.io/pickles/ Data files can be downloaded from interface.
Citation: https://doi.org/10.1093/nar/gkx993
Owner
- Name: franklenoir
- Login: franklenoir
- Kind: user
- Location: United States
- Repositories: 1
- Profile: https://github.com/franklenoir
Citation (citations/citations.txt)
Citation Information PICKLES Database: Lenoir, W.F., T.L. Lim, and T. Hart, PICKLES: the database of pooled in-vitro CRISPR knockout library essentiality screens. Nucleic Acids Res, 2017. Avana Coessentiality Network: Kim, E., et al., Hierarchical organization of the human cell from a cancer coessentiality network. bioRxiv, 2018. shRNA Screens: Hart, T., C. Koh, and J. Moffat, Coessentiality And Cofunctionality: A Network Approach To Learning Genetic Vulnerabilities From Cancer Cell Line Fitness Screens. bioRxiv, 2017. Moffat, J., et al., A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen. Cell, 2006. 124(6): p. 1283-98. GeCKO Screens: Shalem, O., N.E. Sanjana, and F. Zhang, High-throughput functional genomics using CRISPR-Cas9. Nat Rev Genet, 2015. 16(5): p. 299-311. Sanjana, N.E., O. Shalem, and F. Zhang, Improved vectors and genome-wide libraries for CRISPR screening. Nat Methods, 2014. 11(8): p. 783-784. TKOv1 Screens: Steinhart, Z., et al., Genome-wide CRISPR screens reveal a Wnt-FZD5 signaling circuit as a druggable vulnerability of RNF43-mutant pancreatic tumors. Nat Med, 2017. 23(1): p. 60-68. Hart, T., et al., High-Resolution CRISPR Screens Reveal Fitness Genes and Genotype-Specific Cancer Liabilities. Cell, 2015. 163(6): p. 1515-26. Tzelepis-Yusa Screens: Tzelepis, K., et al., A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid Leukemia. Cell Rep, 2016. 17(4): p. 1193-1205. Koike-Yusa, H., et al., Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library. Nat Biotechnol, 2014. 32(3): p. 267-73. Wang Screens: Wang, T., et al., Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras. Cell, 2017. 168(5): p. 890-903 e15. Wang, T., et al., Identification and characterization of essential genes in the human genome. Science, 2015. 350(6264): p. 1096-101. Avana Screens: Doench, J.G., et al., Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9. Nat Biotechnol, 2016. 34(2): p. 184-191. Meyers, R.M., et al., Computational correction of copy number effect improves specificity of CRISPR-Cas9 essentiality screens in cancer cells. Nat Genet, 2017. Sanger (Behan) Screens: Behan, F.M., et al., Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens. Nature, 2019.