BrainSpan genotypes
Friday, December 9th, 2016There are BrainSpan genotypes available through dbGAP:
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000406.v1.p1
There are BrainSpan genotypes available through dbGAP:
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000406.v1.p1
ProtonMail.com: A Gmail Rival [providing encrypted messages] Sent to Siberia by a Mysterious #Google Glitch
http://nytimes.com/2016/11/06/your-money/a-gmail-rival-sent-to-siberia-by-a-mysterious-google-glitch.html
gmail to gmail pop using domains
uses
pop.gmail.com
Use SSL: Yes
Port: 995
with the password as the in the domain (joe@mydomain.com)
This may also require
turning of some of the domain security
https://support.google.com/mail/troubleshooter/6323470#ts=1665162 QT:{{”
Username and password not working? Some apps require you to also turn on access for less secure apps before setting up POP/IMAP connections. “}}
Main one:
http://www.evercontact.com/
auto-updating your gmail contacts by analyzing email signatures:
The other softwares related are:
1) Contactually
(https://www.contactually.com/for-individuals/tour/contact-management/) 2) Signusapp https://signusapp.wordpress.com/
Analysis of high-throughput B-cell sequencing
http://www.pnas.org/content/early/2015/02/05/1417683112.abstract Successful locus-level application of #personalgenome construction
Here is a link for some helpful information on the new NIH format for biosketches:
The discovery of integrated gene networks for autism and related disorders
Fereydoun Hormozdiari
Osnat Penn
Elhanan Borenstein
Evan E. Eichler
Published in Advance November 5, 2014, doi:10.1101/gr.178855.114 Genome Res. 2015. 25: 142-154
QT:{{”
Motivated by this observation, we have developed a novel method that simultaneously integrates information from both PPI and coexpression networks to identify highly connected modules in both types of networks that are also enriched in mutations in cases and not in controls. We call this method MAGI, short for merging affected genes into integrated networks. MAGI is based on a combinatorial
optimization algorithm that aims to maximize the number of mutations in the modules while accounting for gene length and distribution of putative LoF and missense mutations in cases and controls. MAGI is generic and can be applied to any disease, given a list of de novo mutations in cases and relevant coexpression information. Using neurodevelopmental RNA-seq data from the BrainSpan Atlas
(http://www.brainspan.org/), we have applied it to exome sequence data generated from ASD, ID, epilepsy, and schizophrenia, providing a comprehensive comparison of common and specific gene modules for these diseases.
“}}
Experiment.com specializes in funding early-stage research projects by way of “crowd-funding” (similar concept to Kickstarter).
Here is a recent example of the type of research funded: https://experiment.com/projects/what-are-the-patterns-and-effects-of-american-crow-movements
Track-changes in #GDocs, plug-in that provides some functionality. However, wish #Google just had this built-in.
https://chrome.google.com/webstore/detail/track-changes/pgjeblaieehjmmahlikmifaggjckpcnp?hl=en