docm.genome.wustl.edu
DoCM - Database of Curated MutationsBladder transitional cell carcinoma. Lung squamous cell carcinoma. Non-small cell lung carcinoma. Progesterone-receptor positive breast cancer.
http://docm.genome.wustl.edu/
Bladder transitional cell carcinoma. Lung squamous cell carcinoma. Non-small cell lung carcinoma. Progesterone-receptor positive breast cancer.
http://docm.genome.wustl.edu/
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DoCM - Database of Curated Mutations | docm.genome.wustl.edu Reviews
https://docm.genome.wustl.edu
Bladder transitional cell carcinoma. Lung squamous cell carcinoma. Non-small cell lung carcinoma. Progesterone-receptor positive breast cancer.
docm.genome.wustl.edu
DoCM - Database of Curated Mutations
http://docm.genome.wustl.edu/api
The DoCM API allows you to access variant data in a programatic fashion. The DoCM API can be used with simple HTTP requests from any tool or programming language of your choice. This endpoint allows you to retrieve filtered lists of variants in tsv, json, or vcf. Format. Filter parameters can be added to the query string of the request to filter the returned list. You can combine as many filter paramters as you'd like to narrow your query down more effectively. Amino acids=p.Q228P,p.Q61L. To create a ran...
DoCM - Database of Curated Mutations
http://docm.genome.wustl.edu/downloads
Source code to the DoCM web application. This is the full source code of the DoCM web application. It runs Ruby on Rails and Postgres. DoCM versions as flat files. DoCM version 2.1. DoCM version 2.2. DoCM version 3.1. DoCM version 3.2. DoCM versions as ClinVar spreadsheets. DoCM by The McDonnell Genome Institute at Washington University School of Medicine. Is licensed under a Creative Commons Attribution 4.0 International License. You can contact us here.
DoCM - Database of Curated Mutations
http://docm.genome.wustl.edu/about
DoCM, the Database of Curated Mutations, is a highly curated database of known, disease-causing mutations that provides easily explorable variant lists with direct links to source citations for easy verification. Highly curated lists of disease-causing mutations enable researchers and clinicians to foster collaboration and understand the current state of the art of pathogenic variation. Requiring only that attribution be given to the community that created the content. Database Summary (current version).
DoCM - Database of Curated Mutations
http://docm.genome.wustl.edu/faq
FAQ Frequently Asked Questions. How do I cite DoCM? A manuscript for DoCM is currently in preparation. In the meantime please cite http:/ docm.genome.wustl.edu. How do I contribute a variant to DoCM? We welcome candidate variant submissions which will allow this resource to be more comprehensive and useful to the community at large. If you have a submission please fill out a variant submission form. If you would like to contribute your curation efforts to DoCM please contact us. How do I use the DoCM API?
DoCM - Database of Curated Mutations
http://docm.genome.wustl.edu/sources
DoCM, the Database of Curated Mutations, is a highly curated database of known, disease-causing mutations that provides easily explorable variant lists with direct links to source citations for easy verification. DoCM currently captures variants from 876 unique publications. How is the literature curated to produce DoCM? Criteria for inclusion into DoCM. Drug targets associated with a mutation. Diagnostic or prognostic markers associated with a mutation. Disease function described in cell lines. Variants...
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MAGI
http://magi.brown.edu/acknowledgements
MAGI was created by the Raphael research group. MAGI is supported by Brown University, the National Science Foundation and National Institutes of Health. MAGI uses public mutation data from The Cancer Genome Atlas's Pan-Cancer and stomach cancer projects [1-2],. Interaction networks [3-6],. Protein domain databases [7-10]. MAGI also uses annotations from the Database of Curated Mutations. Wildstein, J. et al. 2013) The Cancer Genome Atlas Pan-Cancer analysis project. Nat. Genet. 45, 1113 1120. Letunic, I...
Notes: Bioinformatics Open Source Conference 2015 day 2 afternoon: Translational, Visualization and Lightning Talks | Small Change Bioinformatics
https://smallchangebio.wordpress.com/2015/07/11/bosc2015day2b
Notes: Bioinformatics Open Source Conference 2015 day 2 morning — Ewan Birney, Open Science and Reproducibility. Notes: Bio in Docker Symposium 2015 day 1: ngs pipelines, workflow tools, volume management →. July 11, 2015. Notes: Bioinformatics Open Source Conference 2015 day 2 afternoon: Translational, Visualization and Lightning Talks. I’m at the 2015 Bioinformatics Open Source Conference (BOSC). My other notes from the conference:. Holly Bik and Data Science. Tobias talks about work on defining action...
Faculty | Bioinformatics.ca
https://bioinformatics.ca/workshops/faculty
Skip to Main Content Area. Jobs Alert Mailing List. Bioinformatics Experts in Canada. Bioinformatics Activities in Canada and Worldwide. Education Programs and Courses in Canada. Username or e-mail: *. Bioinformatics specialist and Web Database Developer. Postdoctoral Fellowship in Bioinformatics. Post-Doctoral fellow in High Dimensional Flow Cytometry Bioinformatics. August 19, 2016 -. Bioinformatics.ca has a new YouTube Channel featuring workshop recordings. April 8, 2016 -. March 31, 2016 -. David wor...
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Contact Dr. Lunceford. Check Box to Continue. Contact Dr. Lunceford to Schedule an Appointment. Check Box to Continue. Dr Lunceford provides psychotherapy for adults, couples, children, and adolescents. Life can be challenging in so many ways and. learn more. Approaching legal issues with empathy, expertise and experience in the family court system, personal injury cases, and other. learn more. Dealing with Difficult People. 2356 Moore Street, Suite 100. San diego, California 92110.
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DoCM - Database of Curated Mutations
Bladder transitional cell carcinoma. Lung squamous cell carcinoma. Non-small cell lung carcinoma. Progesterone-receptor positive breast cancer.
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