
Jason Ernst
@jernst98
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Joined February 2015
RT @JasonErnstLab: A new paper: "Genome-wide identification and analysis of recurring patterns of epigenetic variation across individuals"….
nature.com
Communications Biology - Recurring genome-wide patterns of epigenetic mark variation across individuals learned through computational modeling relate to external measures of molecular variation and...
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RT @JasonErnstLab: A new paper: "Identifying associations of de novo noncoding variants with autism through integration of gene expression,….
genomebiology.biomedcentral.com
Background Whole-genome sequencing (WGS) data has facilitated genome-wide identification of rare noncoding variants. However, elucidating these variants’ associations with complex diseases remains...
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RT @JasonErnstLab: A new paper "CMImpute: cross-species and tissue imputation of species-level DNA methylation samples across mammalian spe….
genomebiology.biomedcentral.com
The large-scale application of the mammalian methylation array has substantially expanded the availability of DNA methylation data in mammalian species. However, this data captures only a small...
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RT @JasonErnstLab: A new paper "ChromActivity: integrative epigenomic and functional characterization assay based annotation of regulatory….
genomebiology.biomedcentral.com
We introduce ChromActivity, a computational framework for predicting and annotating regulatory activity across the genome through integration of multiple epigenomic maps and various functional...
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RT @sroyyors: Perspective on recent developments and challenges in regulatory and systems genomics is out, amazing….
academic.oup.com
Abstract. Summary: Predicting how genetic variation affects phenotypic outcomes at the organismal, cellular, and molecular levels requires deciphering the
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RT @biorxiv_bioinfo: Learning a Pairwise Epigenomic and Transcription Factor Binding Association Score Across the Human Genome https://t.c….
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RT @biorxiv_genomic: Identifying associations of de novo noncoding variants with autism through integration of gene expression, sequence an….
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RT @JasonErnstLab: Today October 25th, 2023 is the deadline for late breaking poster submissions to RSGDREAM 2023 being held at UCLA Nov. 2….
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RT @iscb: #RSGDREAM2023 wants YOUR #research #submissions to light up the conference with groundbreaking ideas. Submit Your Research Today….
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RT @JasonErnstLab: Congratulations to @BeyondTheProof on his paper on ChromGene! ChromGene is a method to generate gene-based epigenome ann….
genomebiology.biomedcentral.com
Various computational approaches have been developed to annotate epigenomes on a per-position basis by modeling combinatorial and spatial patterns within epigenomic data. However, such annotations...
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RT @BC_UCLA: We are recruiting new faculty @UCLA @dgsomucla! Pls see the ad below & consider applying. We offer an exceptional academic env….
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RT @biorxiv_bioinfo: Integrative epigenomic and functional characterization assay based annotation of regulatory activity across diverse hu….
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RT @jmuiuc: RECOMB/ISCB RSG 2023 Keynote Speakers include @AnimaAnandkumar @KnightLabNews @drklly @jsb_ucla @RemoRohs @davidvanvalen @JEFwo….
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RT @HaVu_science: Hello! Please check out our new paper just published on @GenomeBiology. This is a sister paper of our previous work on un….
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RT @HaVu_science: Hello! It's a little late but I want to share our recently published manuscript: "A framework for group-wise summarizatio….
academic.oup.com
AbstractMotivation. Genome-wide maps of epigenetic modifications are powerful resources for non-coding genome annotation. Maps of multiple epigenetics mark
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RT @BeyondTheProof: My preprint is out! Thanks so much to @jernst98 and @JasonErnstLab for the support, even after a time away from the lab….
biorxiv.org
Background Computational approaches have been developed and broadly used for annotating epigenomes on a per position basis by modeling combinatorial and spatial patterns within epigenomic data....
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RT @biorxiv_bioinfo: A framework for summarizing chromatin state annotations within and identifying differential annotations across groups….
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