opensnp.org

openSNP

OpenSNP allows customers of direct-to-customer genetic tests to publish their test results, find others with similar genetic variations, learn more about their results by getting the latest primary literature on their variations, and help scientists find new associations. Upload your raw genotyping or exome data from 23andMe. To the openSNP database to make it available for everybody. With openSNP you can share stories about your genetic variations and phenotypes, and discover the stories of other users.

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openSNP | opensnp.org Reviews

<META> DESCRIPTION

OpenSNP allows customers of direct-to-customer genetic tests to publish their test results, find others with similar genetic variations, learn more about their results by getting the latest primary literature on their variations, and help scientists find new associations. Upload your raw genotyping or exome data from 23andMe. To the openSNP database to make it available for everybody. With openSNP you can share stories about your genetic variations and phenotypes, and discover the stories of other users.

<META> KEYWORDS

1 opensnp

2 toggle

3 news

4 data

5 snps

6 genotypes

7 phenotypes

8 phenotypes pictures

9 open humans connections

10 latest data

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opensnp,toggle,news,data,snps,genotypes,phenotypes,phenotypes pictures,open humans connections,latest data,about us,statistics,welcome to opensnp,download data,for genotyping users,upload your genotyping,decodeme,or familytreedna,share your phenotypes

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openSNP | opensnp.org Reviews

https://opensnp.org

OpenSNP allows customers of direct-to-customer genetic tests to publish their test results, find others with similar genetic variations, learn more about their results by getting the latest primary literature on their variations, and help scientists find new associations. Upload your raw genotyping or exome data from 23andMe. To the openSNP database to make it available for everybody. With openSNP you can share stories about your genetic variations and phenotypes, and discover the stories of other users.

INTERNAL PAGES

opensnp.org

1

openSNP | Listing all genotypings

https://opensnp.org/genotypes

Download the dump: Includes all genotyping files plus a CSV with all phenotypes of those users. Python library to parse the provided files. Courtesy of Sergei Lebedev. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as. Right-click and Save as.

2

openSNP | Listing all users

https://opensnp.org/user_index

OpenSNP in the press. Our hosting is made possible thanks to the kind support of Seven Bridges. And its biomedical data analysis platform and our patrons on Patreon. Please consider supporting us as well. If our service is valuable to you! The openSNP project is licensed under the MIT License. The code is at GitHub. The data is donated into the public domain using CC0 1.0. The hand drawn icons were created by one seventy seven. And are licensed under CC BY 3.0.

3

openSNP | openSNP in the press

https://opensnp.org/press

OpenSNP in blogs and press. All links are in English except where noted otherwise. Time-format is dd.mm.yyyy. Sorry, we've been super lazy in updating this. If you want to get a comprehensive list just try Google News. Below is an incomplete list (mostly from 2015). Fusion wrote about us. The BMC Blog featured us. Along with a video of a presentation we gave at BGI's conference. German) German, Austrian and Swiss news outlets ran some articles. About us, our ideas. And the plans we have. What's in a name?

4

openSNP | Listing all phenotypes

https://opensnp.org/picture_phenotypes

Listing all picture phenotypes. Left index finger next to a nickel. OpenSNP in the press. Our hosting is made possible thanks to the kind support of Seven Bridges. And its biomedical data analysis platform and our patrons on Patreon. Please consider supporting us as well. If our service is valuable to you! The openSNP project is licensed under the MIT License. The code is at GitHub. The data is donated into the public domain using CC0 1.0. The hand drawn icons were created by one seventy seven.

5

openSNP | Listing all phenotypes

https://opensnp.org/phenotypes

OpenSNP in the press. Our hosting is made possible thanks to the kind support of Seven Bridges. And its biomedical data analysis platform and our patrons on Patreon. Please consider supporting us as well. If our service is valuable to you! The openSNP project is licensed under the MIT License. The code is at GitHub. The data is donated into the public domain using CC0 1.0. The hand drawn icons were created by one seventy seven. And are licensed under CC BY 3.0.

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opensnp.wordpress.com

A petition on Open Access | openSNP

https://opensnp.wordpress.com/2012/05/23/a-petition-on-open-access

Crowdsourcing genome wide association studies. Go to opensnp.org. A petition on Open Access. We are strong supporters of the open-science movement and are happy to see that there is a new petition aimed at the Obama administration. The goal of this new petition is to make Open Access mandatory for all publications funded by tax-money. This is the full text of the petition. WE PETITION THE OBAMA ADMINISTRATION TO:. The best thing is that you don’t have to be a US citizen to sign the petition. Ju...In tota...

opensnp.wordpress.com

openSNP | crowdsourcing genome wide association studies | Page 2

https://opensnp.wordpress.com/page/2

Crowdsourcing genome wide association studies. Go to opensnp.org. In the last weeks some people contacted us because they wanted to upload their exome-data to. While we started out with a focus on SNP-data (mainly because it’s much more abundant) providing support for exome-data has been on our ToDo-list for a couple of month now, so we did some work on it. Today we start with support for the data which is generated by. So if you’ve got your exome sequenced through. You can now upload it to. Mining liter...

smallchangebio.wordpress.com

July | 2016 | Small Change Bioinformatics

https://smallchangebio.wordpress.com/2016/07

Monthly Archives: July 2016. July 9, 2016. Notes: Bioinformatics Open Source Conference 2016 day 2 afternoon: developer tools and reproducible analyses. I’m at the 2016 Bioinformatics Open Source Conference (BOSC). Day 1 morning notes. X2013; Jennifer Gardy keynote on open data and infectious diseases, plus workflow development. Day 1 afternoon notes. X2013; Talks on standards and a panel on growing communities. Day 2 afternoon notes. Developer tools and libraries. Generates multi-page HTML and amanages ...

genomena.com

Rare variants, disease, and population size – Genomena

http://genomena.com/genomes-and-health/rare-variants-disease-and-population-size

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. Bolstered by th...

genomena.com

Genomes and health – Genomena

http://genomena.com/category/genomes-and-health

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. The plot thicke...

genomena.com

On polymorphism II: Hard-drinking fruitflies – Genomena

http://genomena.com/concepts-genetics-jargon/polymorphism-ii

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. Before Kreitman...

opendatahk.com

Meets Archives - Open Data Hong Kong

https://opendatahk.com/category/events/meets

Meets Archives - Open Data Hong Kong. An Open Knowledge Foundation Site. Research & Communications. Sign up to our mailing list. Hong Kong Data.One portal. Crowdsourcing the Smart City. Crowdsourcing the Smart City. New Methodologies for Participatory Mapping and Civic Co-Management of Urban Environments. Public lecture by Dr. Tomas Holderness. Tuesday, 26 April, 2016. V302, 3/F, Jockey Club Innovation Tower. Hong Kong Polytechnic University. ODHKmeet.32: Hacking the Human Genome. How big is your data?

genomena.com

Genetics, evolution, and policy – Genomena

http://genomena.com/category/genetics-evolution-and-policy

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. On 9 March, Pre...

genomena.com

On twins, genomes, and health – Genomena

http://genomena.com/genomes-and-health/on-twins-genomes-and-health

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. Geneticists hav...

genomena.com

Evolution 101 – Genomena

http://genomena.com/concepts-genetics-jargon

As genomes evolve, so does the world. Three small steps toward genomically sensible healthcare. Harmful by any other name: On clinical variant classification. The Shock of the New: What we can say about HeLa’s novel variants. Harmful by any other name: On clinical variant classification. Genetics, evolution, and policy. TedMed 2010 Your moderator interprets Ozzy Osbourne’s genome. Really. NOVA: Cracking Your Genetic Code Helping explain the prospect of genomically personalized healthcare. New Scientist h...

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openSNP

OpenSNP allows customers of direct-to-customer genetic tests to publish their test results, find others with similar genetic variations, learn more about their results by getting the latest primary literature on their variations, and help scientists find new associations. Upload your raw genotyping or exome data from 23andMe. To the openSNP database to make it available for everybody. With openSNP you can share stories about your genetic variations and phenotypes, and discover the stories of other users.

opensnp.wordpress.com

openSNP | crowdsourcing genome wide association studies

Crowdsourcing genome wide association studies. Go to opensnp.org. Google Summer of Code Wrap-Up. Google Summer of Code. Is drawing to a close so we thought it best to summarise our experience with GS. C from the mentors’ perspective. We originally came to GS. We’ve been having regular calls with Abby Cabunoc. From Mozilla, who’s been kind to support. OBF), which has been participating in GS. C for years. The OBF kindly agreed to take. We came up with 3 projects that we wanted to tackle for quite a while:.

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