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Jiahao Gao

Researcher at Yale University

Publications -  7
Citations -  29

Jiahao Gao is an academic researcher from Yale University. The author has contributed to research in topics: Genome & Personal genomics. The author has an hindex of 2, co-authored 4 publications receiving 7 citations.

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To mock or not: a comprehensive comparison of mock IP and DNA input for ChIP-seq.

TL;DR: In this article, the authors compared DNA input and mock IP and found that mock IPs contain only nonspecific interactions, and the sites predicted from them using DNA input indicate the spurious-site abundance.
Posted ContentDOI

Multi-tissue integrative analysis of personal epigenomes

Joel Rozowsky, +104 more
- 26 Apr 2021 - 
TL;DR: In this paper, the authors constructed phased, diploid genomes for four cadaveric donors (using long-read sequencing) and systematically charted noncoding regulatory elements and transcriptional activity across more than 25 tissues from these donors.
Journal ArticleDOI

Immunological Characteristics of Alternative Splicing Profiles Related to Prognosis in Bladder Cancer

TL;DR: This investigation provided an indispensable reference for ulteriorly exploring the role of AS events in the tumor microenvironment and immunotherapy efficiency, and rendered personalized prognosis monitoring for bladder cancer.
Posted ContentDOI

To mock or not: a comprehensive comparison of mock IP and DNA input for ChIP-seq

TL;DR: A method to use both controls in combination to further improve binding site detection is developed, demonstrating that using a DNA input control results in a definable set of spurious sites, and their abundance is tightly associated with the intrinsic properties of the ChIP-seq sample.
Journal ArticleDOI

The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models

Joel Rozowsky, +100 more
- 22 Nov 2022 - 
TL;DR: The EN-TEx dataset as mentioned in this paper contains 1,635 open-access datasets from four donors (∼30 tissues × ∼15 assays) mapped to matched, diploid genomes with long read phasing and structural variants, instantiating a catalog of >1 million allele-specific loci.