Author

Christopher Ng

Massachusetts Institute of TechnologyORCID 0000-0001-8815-7958Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:CRISPR screen· 1 Approach:experimental assay· 1 Research Focus:perturbation response prediction· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David E. HousmaniD· 2 shared Ahmad Al KhleifatiD· 1 shared Alan Michael PittmaniD· 1 shared Aleksey ShatunoviD· 1 shared Alina L. Li· 1 shared Ammar Al‐ChalabiiD· 1 shared Ashley JonesiD· 1 shared Bradley N. SmithiD· 1 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersNeuroscience

David E. HousmanORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintFeb 19, 2025

CellPHIE: Integrating Pathway Discovery With Pooled Profiling of Perturbations Uncovers Pathways of Huntington's Disease, Including Genetic Modifiers of Neuronal Development and Morphology

Byunguk Kang, Michael A. Murphy, Christopher Ng…·Ernest Fraenkel

The paper integrates pathway discovery with pooled genetic perturbation to identify modifiers of Huntington's disease, revealing genes involved in neuronal development and morphology.

DOI 10.1101/2025.02.19.639023

humanCRISPR screen

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BioinformaticsGenome ResearchPeer-reviewedNov 1, 2017

Detection of long repeat expansions from PCR-free whole-genome sequence data

Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw…·Michael A. Eberle

The paper introduces ExpansionHunter, a tool for detecting long repeat expansions from PCR-free WGS data, achieving high sensitivity and specificity in identifying pathogenic expansions.

388 citations

humanwhole-genome sequencing

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