🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

We are still thrilled to announce ENCODE as the latest AWS Public Data Set! registry.opendata.aws/encode-project/ #OpenScience ENCODE Project

We're announcing Nucleome Browser, an integrative & multimodal data navigation platform for 4DNucleome & the broad community. This tool is a result of tremendous creativity & herculean effort over the years from Xiaopeng Zhu (朱蓬) Yang Zhang, in collab. w/ Jason Swedlow Andrew Belmont 1/n

Our #SMaHTnetwork has #FundingOpps to characterize somatic variation in human tissues, including funding for a Tissue Procurement Center to collect and process a diverse pool of human tissues. Apply by July 8, 2022: go.usa.gov/xzxXR.

**New Funding Announcement** Please take a moment to check out the new SMaHT Funding Opportunities! For more information: commonfund.nih.gov/smaht/fundingo…

Our understanding of cell-type-specific processes in disease development is hampered by the fact that bulk-tissue DNA methylomes are an average of many diverse cell types. How to tackle this problem? Find out about our most recent work with @aetesch just out Nature Methods! 1/7

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

Are you interested in #SomaticMosaicism research? Our #SMaHTnetwork released 5 #FundingOpps to create a catalog of #SomaticMutations in humans and develop state of the art #DNASequencing tools! Apply by July 8, 2022. Learn more: commonfund.nih.gov/smaht/fundingo…

Check out this great opportunity! For more information: abcam.com/events/summer-…

Applying for our #SMaHTnetwork's #FundingOpps to characterize #SomaticMutations in human tissues and develop #genomic sequencing tools? Come to the webinar next Friday from 12 p.m. - 1 p.m. ET to ask questions about the application process: bit.ly/3vyBTgz.

Join our May 10 SeqSPACE webinar to hear about NIH ORIP Precision Disease Modeling Initiative and its functional & phenotypic analysis of disease-causing variants in model organisms. Details: epi.grants.cancer.gov/events/seqSPAC… BCMHouston The Jackson Laboratory UAB

My first book chapter is out in Methods in Molecular Biology! I couldn't be happier! 🎉🎉🎉 link.springer.com/protocol/10.10… #Genomics #Epigenomics #EWAS

DataWorks! Prize Announced! The Federation of American Societies for Experimental Biology (FASEB) and the National Institute of Health (NIH) are championing a bold vision of data sharing and reuse. For more info about the DataWorks! Prize: challenge.gov/?challenge=dat…

Our work on the epigenomics of lung function is out now! doi.org/10.1164/rccm.2… (1/8)

Our understanding of disease variants in minorities is hampered by the fact that many epigenomic datasets are not available for certain populations. How to tackle this problem? Find out about our work with @NoraFranceschi2 just out Nature Genetics! nature.com/articles/s4158… 🧵 1/9

We queried public ENCODE Project epigenomic datasets for different statistical metrics relating to race/ethnicity/country of origin, finding only 42.7% of experiments reporting any race or ethnicity information. The way forward here: SNP-based ancestry imputation across all samples

Check out the IGVF website and the new IGVF logo at igvf.org #IGVF

So glad our work on diversity in EWAS is finally out! 🎉 genomemedicine.biomedcentral.com/articles/10.11… #genomics #epigenomics #EWAS #diversity 🧵 1/

Interested in Program Director positions National Human Genome Research Institute? We have an exciting opportunity for a Program in Genome Science. Application period is September 21-30. genome.gov/careers-traini…

Are you studying genomic variants and looking for a method that provides eQTL, chromatin looping, epigenetic mark, TF binding sites, and other data? Check out the new FORGEdb web tool biorxiv.org/content/10.110… 🧵

The IGVF Consortium has posted two new workshops to our YouTube channel: MPRA design and Post-GWAS analyses. Subscribe to learn more about the Impacts of Genomic Variation on Function: youtube.com/channel/UCn0l0…