ENCODE Project
@ENCODE_NIH
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The ENCODE Project at NHGRI/NIH aims to identify functional DNA elements in human and mouse genomes. Disclaimers: https://t.co/4hdQRFkFNU
Bethesda, MD
Joined April 2012
We are excited to announce the release the ENCODE 3 publication package consisting of an Encyclopedia paper, perspective and 14 papers spanning topics of human and mouse gene expression, regulation, epigenetics, disease and software tools! https://t.co/jhl1fG4B8a
nature.com
How cells, tissues and organisms interpret the information encoded in the genome has vital implications for our understanding of development, health and ...
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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
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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 https://t.co/bhrnzTMNLJ 🧵
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Interested in Program Director positions @genome_gov? We have an exciting opportunity for a Program in Genome Science. Application period is September 21-30.
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So glad our work on diversity in EWAS is finally out! 🎉 https://t.co/Nouye1nkEW
#genomics #epigenomics #EWAS #diversity 🧵 1/
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Check out the IGVF website and the new IGVF logo at https://t.co/DHv2c0yA5p
#IGVF
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We queried public @ENCODE_NIH 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
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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 @NatureGenet! https://t.co/6Di5JqFAyk 🧵 1/9
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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.gov is the official government website supporting prize challenges and prize competitions that are sponsored by the US federal government. Here federal agencies provide prize awards to...
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My first book chapter is out in Methods in Molecular Biology! I couldn't be happier! 🎉🎉🎉 https://t.co/WZnuY0552Y
#Genomics #Epigenomics #EWAS
So glad my latest preprint is out now! Cell type-specific signal analysis in EWAS https://t.co/nWLd1RUPGz (1/9)
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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: https://t.co/JD4IVH2RiS
@bcmhouston @jacksonlab @UABNews
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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: https://t.co/VsDtDX0oaZ.
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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: https://t.co/j12i9uV27a
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We are still thrilled to announce ENCODE as the latest AWS Public Data Set! https://t.co/wciuH7cBca
#OpenScience @ENCODE_NIH
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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: https://t.co/qLPou3x52A
#ResearchAllofUs
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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 @naturemethods! 1/7
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**New Funding Announcement** Please take a moment to check out the new SMaHT Funding Opportunities! For more information:
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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: https://t.co/qWwNAERuMs.
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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 @nimezhu @zocean636, in collab. w/ @jrswedlow @belmont_andrew 1/n
Nucleome Browser: An integrative and multimodal data navigation platform for 4D Nucleome https://t.co/UkczkYDZV2
#bioRxiv
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