Where should you go to pursue your Ph.D. or postdoc? Science Careers asked researchers how they made their decision: scim.ag/2MkGgmZ

February #FeatureArticle - "Physicians’ perspectives on receiving unsolicited genomic results" #SharedIt rdcu.be/bmYFD

Role of Structural Iatrogenesis in Opioid Crisis

Genetics in Your Practice is a unique opportunity for primary care providers to learn how #genetics and #genomics can be applied in the primary care setting. Register for this half-day ACMG workshop in Seattle in conjunction with #ACMGMtg19 ow.ly/Cb8I50lTswT

Platelet decoys inhibit thrombosis and prevent metastatic tumor formation in preclinical models stm.sciencemag.org.pitt.idm.oclc.org/content/11/479…

On #RareDiseaseDay 2019, read our recent #Editorial: Spotlight on rare diseases for #free here hubs.ly/H0ggC_g0 #RareDiseases #ShowYourRare @RareDiseaseDay

Genomic databases are heavily skewed toward people of European descent. If left unaddressed, this inherent bias will continue to contribute to uneven success rates in #PrecisionMedicine. scientificamerican.com/article/we-nee… #diversity #genomics #pharmacogenomics via @SciAm

The ten commandments for learning how to code nature.com/articles/d4158…

Heritability of skewed X-inactivation in female twins is tissue-specific and dependent on age biorxiv.org/cgi/content/sh… #biorxiv_genetic

The Genomic Landscape of Endocrine-Resistant Advanced Breast Cancers @Sloan_Kettering Cancer Cell #AACR19 bit.ly/2FIDVRu

Benefits and limitations of GWAS nature.com/articles/s4157…

Careful benchmarking of ~70 different methods for SV detection from human genomes: genomebiology.biomedcentral.com/articles/10.11… Looks to be an impressively comprehensive and valuable reference to guide future SV discovery efforts. Thank you to the authors for compiling this study!!

So excited about the upcoming primary care clinic for precision medicine in Pittsburgh 🧬💊💉

I’m not a big fan of the commonly seen *, **, *** system for denoting p-values on graphs. Let’s embrace 21st century symbology and do better: p < 0.1 🤥 p < 0.05 🤔 p < 0.01 🙂 p < 0.001 🤩 p < 0.00000001 🤯

Thrilled to announce the release of gnomAD v3, a catalogue of 700M genetics variants based on WGS from 71k samples! It is our first release mapped to GRCh38 and represents a massive leap in analysis power for all non-coding analysis using gnomAD.

Is your poster missing a key phrase in the title?! Grab a card from the center of the exhibit hall. Together we can highlight research being done in diverse populations! #ASHG19 #genomicdiversity

Exciting publications and findings from #PCAWG Pan-Cancer Analysis of Whole Genomes.A collection of research and related content from the ICGC/TCGA consortium on whole-genome sequencing and integrative analysis of cancer nature.com/articles/d4285…

NEWS 🎉: All of Us has released its first genomic dataset, which includes whole genome sequences from nearly 100K participants, in addition to genotyping arrays on 165K participants from diverse backgrounds. #Researchers, learn more: bit.ly/3N1vEtO #ResearchAllofUs

If any one has interested in mouse genetics and imaging, my lab is looking for a technician. Ideal candidate has some wet lab skills and is looking for some computational experience or vice-versa. cfopitt.taleo.net/careersection/…