//
sign in
Profile
by @danabra.mov
Profile
by @dansshadow.bsky.social
Profile
by @jimpick.com
AviHandle
by @danabra.mov
AviHandle
by @dansshadow.bsky.social
AviHandle
by @katherine.computer
EventsList
by @katherine.computer
ProfileHeader
by @dansshadow.bsky.social
ProfileHeader
by @danabra.mov
ProfileMedia
by @danabra.mov
ProfilePlays
by @danabra.mov
ProfilePosts
by @danabra.mov
ProfilePosts
by @dansshadow.bsky.social
ProfileReplies
by @danabra.mov
Record
by @atsui.org
Skircle
by @danabra.mov
StreamPlacePlaylist
by @katherine.computer
+ new component
ProfilePosts









Loading...
Outreach from @TNTurnerLab @washugenetics.bsky.social: We have built new state of the art #genomics software out of necessity for current research on neurodevelopmental disorders, and it’s proving useful beyond NDDs. First white paper out today: CNPI (zenodo.org/records/1884...) #GenomicsWhitePapers
Excited to share a new paper on sex-aware genome-wide assessment of de novo variants (DNVs) in autism. The complete DNV callset and supplementary analyses are available in the Supplement to the paper. link.springer.com/article/10.1... #genomics #genetics #denovo #autism @washugenetics.bsky.social
"Sex Limited Inheritance in Drosophila" #classic #genetics www.jstor.org/stable/1635471
"A novel homecage operant paradigm reveals circadian and behavioral dynamics of social motivation in mice" www.biorxiv.org/content/10.1...
WashU Rare Disease Day was wonderful today. Stephanie Snow-Gebel gave my favorite talk, and this quote really stuck with me: “Awareness is not vanity. It’s velocity!” 🔥 @rarediseaseday.bsky.social @pattidickson.bsky.social #SnowFoundation
The faster you can analyze data, the faster discovery follows. New tools from The Turner Lab, led by tycheleturner at #WashU, are on #CAVATICA. Streamline how researchers analyze #KidsFirstData and help them turn discovery into insight faster. Explore how: https://monkeylink.co/7b09d7
3mo
4d
3mo
10d
3mo
3mo
link.springer.com
Human Genomics - Autism spectrum disorder (ASD) shows a consistent sex bias, yet how sex shapes de novo variant (DNV) risk across coding and noncoding sequence remains unclear. I analyzed DNVs...
Sex-aware genome-wide assessment of de novo variants in autism across coding and noncoding regions - Human Genomics
T. H. Morgan, Sex Limited Inheritance in Drosophila, Science, New Series, Vol. 32, No. 812 (Jul. 22, 1910), pp. 120-122
www.jstor.org
Sex Limited Inheritance in Drosophila on JSTOR
www.biorxiv.org
White Paper for CNPI TNTurnerLab, Washington University School of Medicine
zenodo.org
White Paper: "Copy Number Private Investigator (CNPI): making rare copy number changes usable at scale"
Gabriella Miller Kids First Data Resource Center
❄️ Introducing SNOW - the Second-pass de Novo variant Offspring Workflow. A Python toolkit for cleaning, merging, phasing, and annotating de novo variants from trio sequencing data for QC and downstream analysis ☃️ github.com/tycheleturne... #genomics #bioinformatics #denovo
www.nikonsmallworld.com/galleries/20... #cochlea #ear #microscope
3mo
2mo
Second-pass de Novo variant Offspring Workflow. Contribute to tycheleturner/snow development by creating an account on GitHub.
github.com
GitHub - tycheleturner/snow: Second-pass de Novo variant Offspring Workflow
@tycheleturner.bsky.social and the Turner lab were recently highlighted by the Gabriella Miller Kids First Data Resource Center kidsfirstdrc.bsky.social for developing CAVATICA genomic analysis tools that streamline the path from Kids First data access to analysis. kidsfirstdrc.org/turner-lab-t...
2d
The Gabriella Miller Kids First Data Resource Center (Kids First DRC) is a collaborative pediatric research effort with a goal to understand the genetic causes and links between childhood cancer and c...
kidsfirstdrc.bsky.social
Gabriella Miller Kids First Data Resource Center (@kidsfirstdrc.bsky.social)
"Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)" www.cell.com/ajhg/fulltex...
3mo
Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
Age-related hearing loss (presbycusis) is a significant problem in the population. The genetic contribution to age-related hearing loss is estimated to be 40%–50%. Gene mutations that cause nonsyndrom...
WashU Medicine Genetics
www.cell.com