My lab is looking for a bioinformatics postdoc to develop computational algorithms for somatic mutation discovery, as part of NIH's new SMaHT Initiative. Exciting new project in my lab. See job posting at https://t.co/tuzHNo5iZD or contact me directly at [email protected].
Excited to release a free version of our genomic visualization & analytics platform, Mosaic. Add unlimited samples (AWS S3 so far). Organize projects across buckets, add teammates, & better understand your data. https://t.co/BlUaWr38AS . Overview Video https://t.co/LrYUlUwY6B
A brand new https://t.co/NpfgJoYquZ app just out! https://t.co/IpJUE8DSYk helps you create a list of candidate genes corresponding to the patient's disease and phenotype, using commercially available panel tests. Details at: https://t.co/Mi4lxP82F6 .
In our new manuscript, we used WGS and comprehensive variant detection to diagnose 14/14 patients w/ EIEE. We implicated two new genes and found pathogenic SVs (one dup and one translocation) affecting two known EIEE genes. Great collab with Neurology! https://t.co/QjDpPlRnfr
Our study achieving high diagnostic rate in early childhood seizures via whole-genome sequencing is out in Nature Genomic Medicine! Read at: https://t.co/KgzOrKnmdR. Great job @aaronquinlan, Josh, Betsy, Russ, @brent_p , Andrew, @ryanlayer, @tony_disera, Al, Chase, et al.!
This is a really nice upgrade! Takes gene.iobio from a single-gene analysis tool to multi-gene analysis. Also, clean new interface look. https://t.co/kXxD29AAhG
https://t.co/eOlJ36YkEL v2.1 with nice new features! Also updated https://t.co/zkjckhEsyy & https://t.co/VG9qTJViZr. All built with dev kit. https://t.co/D3Zh0CNxjv