September 2008 - August 2016
We study the genetic basis of the neural circuits underlying innate behaviors and how these circuits function in the behaving animal. We use the mating behavior of the fruit fly Drosophila melanogaster as a model.
July 2007 - July 2014
How does electrical activity in neuronal circuits give rise to intelligent behavior? To answer this question, we are pursuing two synergistic research directions.
September 2008 - February 2014
Our laboratory has a long-standing and continuing interest in this extrachromosomal genome, mainly in the areas of mtDNA replication and transcription.
September 2010 - August 2015
The advance of optical technologies has revolutionized a broad range of biomedical research fields. During the past two decades, novel optical imaging techniques have been developed to provide unprecedented resolution, sensitivity, and speed. However, the optical penetration depth in tissues remains very limited.
January 2013 - December 2017
What makes one’s brain a brain? Our lab is interested in elucidating the relationship between behavior and the underlying neuronal circuit structure and neural population dynamics.
July 2006 - June 2015
Genome sequences are now known for thousands of different species. We are at a remarkable time in biology where at last we can look at the "source code" for life—the DNA sequences that specify development, regulation, and function of organisms—but we are still far from adequately understanding how to read this vast trove of encoded information or being able to reconstruct how it evolved.
January 2008 - January 2015
Roian Egnor uses multi-generational groups of socially-housed mice to study the neural basis of complex vocal and social behavior.
May 2012 - September 2015
The Fetter lab is interested in developing tools and techniques to faithfully preserve the in vivo biological structure and maximize information content at nanometer resolution for the next generation of Drosophila EM connectomes.
March 2014 - October 2016
Exploring neural computation in behaving animals at the scale of large populations and entire brains, through a combination of collaborative data analysis and experimental design across multiple model systems, and developing technology for modern computational science.
September 2014 - June 2018
Our laboratory studies the structures of membrane proteins important in homeostasis and signaling. We develop new tools in structural biology, namely MicroED as a new method for cryo EM, to facilitate the study of such membrane proteins to atomic resolution from vanishingly small crystals.
August 2008 - April 2011
The Gustafsson Lab was dedicated to creating new forms of light microscopy for biological imaging.
February 2011 - January 2014
Electron microscopy (EM) is still the best technique for producing data from which one can unambiguously determine the complete synaptic connectivity of neuronal assemblies.
February 2011 - January 2018
We develop optical methods for in vivo imaging and apply these methods to structural and functional studies of neural circuits.
November 2016 - May 2018
The lab will focus on automated reconstruction and identification of neurons in EM and light microscopic image data of the fly brain, where the goal is to exploit prior knowledge about global neuron shapes. This will enable biologists to find specific neurons of interest efficiently in huge EM volumes. Furthermore, it will be exciting to map circuits known from EM onto functional acquisitions to be able to observe known circuits in action. Therefore, the respective specific cell bodies have to be identified in functional imaging data.
September 2006 - August 2013
How does an organism compute its behavior? The Kerr lab seeks to answer this question for one of the simplest model organisms, the nematode worm Caenorhabditis elegans.
August 2006 - July 2018
Our ultimate goal is to provide a mechanistic understanding of a behaviorally relevant brain function.
To this end we are attempting to produce biophysically based explanations of the information-processing and storage capabilities of single and small networks of neurons. We use a variety of optical (two-photon transmitter uncaging, single and two-photon ChR2/NpHR activation, two photon Ca2+ imaging) and electrical (dual whole-cell recordings, cell-attached and outside-out patches) techniques in the various projects.
September 2016 - April 2018
Simultaneous advances in biochemical techniques and computing power in the early 21st century have transformed the field of biology by allowing for the generation of comprehensive large-scale molecular datasets. At Janelia, we will characterize cell types in the brain using transcriptome-wide data from single cells and small populations of cells to uncover the molecular grammar underlying the components of the nervous system and their connections. Ultimately, linking gene expression and epigenetic information to other phenotypes – including lineage, neuronal connectivity, and cell-cell communication – is crucial to understanding the control of neuronal identity.
September 2009 - August 2015
Determining the properties and salience of sensory cues is fundamental to the survival and characteristic behavior of most, if not all, organisms. Our lab identifies mechanisms that underlie the sensitivity and selectivity with which neurons in the mammalian nervous system respond to visual stimuli.
September 2005 - May 2012
The Myers Lab is developing algorithms and software for the automatic interpretation of images produced by light and electron microscopy of stained samples, with an emphasis on building 3D and 4D "atlases" of brains, developing organisms, and cellular processes.
January 2010 - August 2016
The hippocampus is the region of the brain that is necessary for the formation and storage of episodic memories - unique events we experience in our lives as "I just met my best friend and we went for a walk." We study what firing patterns of hippocampal neurons are responsible for encoding and recall of these memories.
November 2007 - August 2012
Hanchuan Peng develops bioimage analysis and informatics techniques. He uses these techniques to mine and fuse knowledge from three-dimensional animal brain images, at both micrometer and nanometer scales. His group is building 3D neuronal atlases of brains – incorporating neuron distribution, projection, and connection statistics and mapping functional data of neurons.
October 2007 - September 2016
We are interested in how the developmental hormones, ecdysone and juvenile hormone, interact to allow and orchestrate metamorphosis.
August 2006 - August 2012
Our lab is using electrophysiology, optogenetics, and psychophysics to understand the principles of sensory information processing. Specifically, we are focused on two questions: 1) how is odor information coded in the brain of the awake, behaving mouse? And 2) how is information relevant to animal behavior extracted by the brain? In short, we want to know what the mouse’s nose tells its brain.
July 2006 - July 2015
We use genetic tools and screening strategies to identify the specific neurons necessary and sufficient to control grooming and feeding, behaviors which were chosen for their sequential progression and cue integration properties.
April 2009 - September 2016
Robert Tjian is interested in the biochemistry of gene regulation in humans and animals. In particular, what is the nature of the molecular machinery that controls the turning up and down of gene expression in human cells, and how does disruption of this highly regulated process lead to various disease states?
July 2009 - February 2015
Our long-term goal is to elucidate mechanisms used for signal transduction and information processing in sensory systems and to understand how the senses create an internal representation of the outside world.