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people

Trygve Bakken

Investigator, Assistant

teams /
Allenite

Trygve Bakken maps the vast diversity of cell types in the human brain and compares them to other species to understand how our brains develop, evolve, and change in disease. By pairing large-scale single-cell genomics with genetic tools for precise circuit access, his work lays the groundwork for new approaches to study and treat brain disorders. Dr. Bakken joined the Allen Institute in 2013 after earning his M.D. and Ph.D. in Neuroscience at the University of California, San Diego, where he investigated the genetic basis of human brain morphology and developmental principles of neural circuitry. He also holds an M.Sc. in Philosophy and History of Science from the London School of Economics and a B.A. in Physics and Philosophy from Yale University.

research focus

Dr. Bakken leads cross-species studies of neural cell type diversity using high-throughput, multiomic profiling of single nuclei from the human brain and other mammals. His research defines conserved and human-specialized molecular phenotypes of mammalian brain cell types. His team develops machine learning models to predict in vivo activity of cell type-specific enhancers, enabling the systematic design of viral tools for precise access to targeted neuronal and non-neuronal populations. These enhancer-AAV tools, validated across rodents and non-human primates and distributed via the Genetic Tools Atlas, provide standardized resources for probing neural circuits and informing therapeutic strategies.In earlier studies, Dr. Bakken generated transcriptional atlases of primate cortical development, revealing conserved and uniquely human developmental trajectories and implicating specific cell populations in psychiatric risk for autism spectrum disorder and schizophrenia. He has also linked variation in cell type abundance and gene expression to age, sex, genetic background, and evolutionary history, and demonstrated how ancient human population movements have shaped cortical architecture. Ongoing work extends these approaches across additional human donors and species to connect molecular, developmental, and functional perspectives on brain organization, evolution, and disease.

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featured contributions
featured media
featured stories
featured events
featured publications

featured events

event / October 25 - 29, 2026
2026 Lake Conference – Comparative and Evolutionary Neurobiology
Join the Allen Institute and Circuit Neuroscience Basel for the Lake Conference in Seattle, Washington this October.

featured stories

news
Allen Institute Announces 2022 Next Generation Leaders
Six early-career neuroscientists will help guide research into the complexities of the mammalian brain
news
New insights about evolution of human brain region that controls voluntary movement, including rare, large neurons vulnerable in ALS
Is our brain like that of a mouse or a monkey? New study aims to find our cellular similarities - and key differences

featured media

media / Allen Institute
KOMO Seattle: How new biological tools are changing the game in the battle against brain disease
Researchers across North America have teamed up to create an arsenal of biological tools to play a critical role in the battle against brain disease.
media / Washington Post
The Washington Post: Scientists develop gene delivery ‘trucks’ that could treat brain diseases
Gene delivery systems can target specific brain cells, leading to treatments for Parkinson's, Alzheimer's and other neurodegenerative diseases.

featured publications

publication / 2025
Integrating multimodal data to understand cortical circuit architecture and function
Nature Neuroscience
publication / 2024
Applying single-cell and single-nucleus genomics to studies of cellular heterogeneity and cell fate transitions in the nervous system
Nature Neuroscience
publication / 2024
Distinctive physiology of molecularly identified medium spiny neurons in the macaque putamen
Cell Reports
publication / 2023
Transcriptomic diversity of cell types across the adult human brain
Science (New York, N.Y.)
publication / 2023
Signature morphoelectric properties of diverse GABAergic interneurons in the human neocortex
Science (New York, N.Y.)
publication / 2023
A comparative atlas of single-cell chromatin accessibility in the human brain
Science (New York, N.Y.)
publication / 2023
Comparative single-cell transcriptomic analysis of primate brains highlights human-specific regulatory evolution
Nature Ecology & Evolution
publication / 2021
A multimodal cell census and atlas of the mammalian primary motor cortex
Nature
publication / 2021
A machine learning method for the discovery of minimum marker gene combinations for cell type identification from single-cell RNA sequencing
Genome Research
publication / 2021
Single-cell and single-nucleus RNA-seq uncovers shared and distinct axes of variation in dorsal LGN neurons in mice, non-human primates, and humans
eLife
publication / 2020
Common cell type nomenclature for the mammalian brain
eLife
publication / 2019
New insights into the development of the human cerebral cortex
Journal of Anatomy
publication / 2019
Identification of genetic markers for cortical areas using a Random Forest classification routine and the Allen Mouse Brain Atlas
PloS One
publication / 2018
Shared and distinct transcriptomic cell types across neocortical areas
Nature
publication / 2018
Cell type discovery using single-cell transcriptomics: implications for ontological representation
Human Molecular Genetics
publication / 2017
Cell type discovery and representation in the era of high-content single cell phenotyping
BMC bioinformatics
publication / 2017
PRODUCTION OF A PRELIMINARY QUALITY CONTROL PIPELINE FOR SINGLE NUCLEI RNA-SEQ AND ITS APPLICATION IN THE ANALYSIS OF CELL TYPE DIVERSITY OF POST-MORTEM HUMAN BRAIN NEOCORTEX
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
publication / 2014
Convergent transcriptional specializations in the brains of humans and song-learning birds
Science (New York, N.Y.)
publication / 2014
Disruptive CHD8 mutations define a subtype of autism early in development
Cell
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