Rotation Opportunities

Working in the Parker Lab

Below is a list of Bioinformatics affiliated faculty with rotation opportunities in their labs. Nearly all faculty are potential rotation mentors, however specific rotation opportunities are listed below. These research options are available for both first year graduate students and Master’s students. If there is a particular faculty member you would like to work with who is not listed, you are encouraged to contact them to learn of future 

For students interested in a lab rotation with a PIBS faculty member, a list of affiliated PIBS faculty and their respective research topics are available here: 

https://www.umms.med.umich.edu/faculty-search/search-results?program=BIOI

Current Rotations Opportunities

Department of Computational Medicine and Bioinformatics (DCMB) 

Alan Boyle (Computational Medicine & Bioinformatics)

E-Mail: apboyle@umich.edu

We use modern genomics techniques and high-throughput experiments to explore biological systems. We can leverage wet lab and computational tools to help answer biological problems that were previously intractable. We aim to combine computational approaches with high-throughput biological assays to better understand the whole human transcriptional regulatory system. A detailed description of my lab's research interests, and a list of recent publications, can be found on the Boyle lab web site: http://BoyleLab.org.
Specific projects include variations on:

  1.  Logic of gene regulatory control
  2.  Machine learning tools for predicting the effect of variants on gene regulation
  3.  Regulatory effect on gene splicing and its effect on breast cancer
  4.  Analysis of enhancer-promoter interactions
  5.  Genome-wide screens of enhancers, promoters, silencers, and enhancer blockers
  6.  Study of the efficiency of the CRISPR system

Ivo Dinov (Computational Medicine & Bioinformatics/Nursing)

E-Mail: dinov@umich.edu

The Statistics Online Computational Resource (SOCR) develops, validates and shares resources for scientific computing, predictive big data analytics, statistical computing, and decision support. We welcome students, fellows, trainees and researchers interested in participating in SOCR projects (http://SOCR.umich.edu) and collaborating with faculty and researchers on advanced analytics, biomedical informatics, and high-throughput health information technologies.

Yuanfang Guan (Computational Medicine & Bioinformatics)

E-Mail: gyuanfan@umich.edu

Potential projects includes:

  1. Developing tools to predict disease-related genes based on genomics data.
  2. Integrating data to study functional interactions between proteins (biological networks).
  3. Predicting pathways.

Ability to program is required; have to be interested to learn biology.

Alla Karnovsky (Computational Medicine & Bioinformatics)

E-Mail: akarnovs@umich.edu

Metabolomics is a rapidly developing field that uses a variety of analytical methods to detect small organic molecules and follow their changes in tissues and biofluids.

I am interested in developing new methods and tools for the analysis of metabolomics data and integrating them with other omics data. We recently developed a tool called Metscape for the analysis and visualisation of metabolomics data (http://metscape.ncibi.org/). It allows users to build and analyze networks of genes and compounds, identify enriched pathways from expression profiling data, and visualize changes in metabolomics data. As more and more metabolomics data sets become available there is great interest in more sophisticated data analysis methods. Several possible projects in this area include developing new methods for metabolite enrichment analysis, predicting metabolite changes based on transcriptome and proteome, and building disease metabolite networks.

Jeffrey Kidd (Computational Medicine & Bioinformatics)

E-Mail: jmkidd@umich.edu

Several projects related to genomics research including:

  • structural and copy number variation in domestic dogs
  • retroelement insertion polymorphism in domestic dogs
  • assessment of genome assembly algorithms for determining rearrangement breakpoints
  • evolution of pseudo-autosomal regions in non-human primates
  • investigation of allele frequency data for disease genes in non-human primates
  • inference of human demographic history from full genome sequence data

Jacob Kitzman (Computational Medicine & Bioinformatics/Human Genetics)

E-Mail: kitzmanj@umich.edu

Several rotation projects are available involving technology development for massively parallel sequencing and high-throughput functional analysis.

One major goal of our current work is to use massively parallel mutagenesis coupled with functional screens to systematically measure the effects of all possible mutations to genes implicated in cancer and other disorders. We then use these large-scale measurements, along with lists of known pathogenic and neutral variants, to train models to prospectively classify all other alleles as to their pathogenicity. (see e.g., Kitzman et al Nature Methods 2015, or Starita et al, Genetics, 2015).

Rotation students with either computational or experimental backgrounds (or both) are welcome. Please email Jacob (kitzmanj@umich.edu) or stop by (4811 Med Sci II) to learn more.

Matthias Kretzler (Computational Medicine & Bioinformatics/Internal Medicine)

E-Mail: kretzler@umich.edu

The research in Dr. Kretzler’s team focuses on the analysis of molecular mechanism of glomerular failure. Using integrated biology approaches the group defines transcriptional networks in human glomerular diseases and integrates them with complex clinical data sets and other large-scale data sets. The NEPTUNE network offers the unique opportunity to analyze a prospective cohort of glomerular disease patients with high-resolution clinical and molecular phenotyping. An international multi-disciplinary research team will enable large scale data integration across the genotype-phenotype continuum of glomerular failure with carefully monitored environmental exposures, genetic predispositions, epigenetic markers, transcriptional networks, proteomic profiles, metabolic fingerprints, digital histological biopsy archive and prospective clinical disease characterization.

Opportunities for bioinformatics graduate student rotations include integrative analyzes across species along the genotype-phenotype continuum in an interdisciplinary research team.

Possible projects include work on strategies for (1) integrating systems information into genetic association analyses, (2) identifying molecular subsystems affected by multiple candidate genetic variants, and (3) identifying shared mechanisms across tissues, species, or phenotype.

Expansion of the project into a Ph.D. thesis is possible and funds for support might be available.
Background in analysis of large-scale data sets is preferred; basic concepts of molecular biology, statistics and programming are required; and ability to function and interact in a multidisciplinary team is essential.

Jun Li (Computational Medicine & Bioinformatics/Human Genetics)

E-Mail: junzli@umich.edu

Professor Li's rotation opportunities focus on aspects of quantitative analysis in statistical genetics, biomedical data science, or cancer genomics. Current open projects include: single-cell RNAseq data analysis, application of single-cell RNAseq in studying germ cell development and cancer relapse, methodological and theoretical research in clustering, mutation patterns in the human genome, multi-omics data integration involving metabolomic, proteomic, and transcriptomic data, QTL mapping in rat models of metabolomic traits and emotional traits.

Rajasree Menon (Computational Medicine & Bioinformatics)

E-Mail: rajmenon@umich.edu

My main research is on the role of alternative splice variants in human cancers. Experience in some programming and statistics will be an advantage.

Kayvan Najarian (Computational Medicine & Bioinformatics)

E-Mail: kayvan@umich.edu
Website: najarianlab.ccmb.med.umich.edu

Traumatic brain injury (TBI) is a major cause of disability and death and each year around two millions TBI occur in the United States with the approximately 3% of mortality across all TBI severities. About 50% of the deaths are within the first two hours after injury. Therefore, the speed and accuracy are vital in diagnosing the TBI for which a computer-aided trauma decision making system can help reduce mortality, long-term complications, and the associated costs. Developing such a system is challenging due to the inherent noise associated with images, quality of the images, different scales and capturing orientations of the images, variation in the size, shape and location of ventricles from patient to patient, etc. A fully-automated system to identify and assess traumatic brain injury and specially localize the damage would be beneficial in guiding real-time clinical diagnosis as well as quality assurance. The proposed project intends to design a fully-automated system to utilize advanced image processing and machine learning techniques to analyze CT brain images independent of human input. Our preliminary results show the promising results of the proposed system. We also intend to integrate and combine the information in CT images with other patient data (clinical, molecular, physiological, etc) to further improve the predictions / recommendations generated by the system.

Alexey Nesvizhskii (Computational Medicine & Bioinformatics/Pathology)

E-Mail: nesvi@umich.edu

Alexey Nesvizhskii Lab has rotation opportunities in proteome informatics. Projects in the lab include 1) Development of computational methods for large-scale proteomics; 2) Analysis of protein-protein interaction data; 3) Integrative analysis across multiple omics datasets (RNA-seq transcriptomics, proteomics, etc.).

Stephen Parker (Computational Medicine & Bioinformatics)

E-Mail: scjp@umich.edu

Our research group uses an integrative approach in the general fields of computational biology and functional genomics. The major goal of the lab is to generate mechanistic knowledge about how disease susceptibility is genetically encoded in the non-coding portion of the genome, with a focus on type 2 diabetes (T2D). We accomplish this through an interdisciplinary combination of molecular/cellular and computational methods – we generate multiple high-throughput data sets on the genome, epigenome, transcriptome, and proteome across the human population and diverse species and in disease-relevant tissues/cells and use computational approaches to integrate and analyze this data.

We contribute to multiple international consortia:

  • FUSION (Finland-United States Investigation of NIDDM genetics)
  • AMP-T2D (Accelerating Medicines Partnership for T2D)
  • TOPMed (Trans-Omics for Precision Medicine)
  • InsPIRE (Integrated Network for Systematic analysis of Pancreatic Islet RNA Expression)
  • MoTrPAC (Molecular Transducers of Physical Activity Consortium)

Projects spanning the lab and these consortia offer many exciting rotation opportunities.

Additional details can be found at the lab web site: http://theparkerlab.org
If you have any questions, or would like to discuss rotations, please feel free to contact Steve at scjp@umich.edu

Indika Rajapakse (Computational Medicine & Bioinformatics)

E-Mail: indikar@med.umich.edu

I have potential projects related to:

  • Dynamics of the three dimensional structure of the human genome
  • The Biochronicity Program at the Defense Advanced Research Projects Agency.

If you're very creative and would like to work at the interface of mathematics and biology, please contact me, I would love to discuss potential projects.

Maureen Sartor (Computational Medicine & Bioinformatics)

E-Mail: sartorma@umich.edu

We have multiple exciting rotation opportunities in our lab! The focus of my laboratory is developing bioinformatics methods and tools for the analysis and interpretation of high-throughput molecular biology data, with special focus on gene regulatory and epigenomics data from next generation sequencing experiments. The biological focus of my laboratory is cancer and epigenomics, in particular oropharyngeal/oral squamous cell carcinomas (OP/OSCC). Rotation projects are available working with OP/OSCC data, including CNV, RNA-seq, and DNA methylation data from two important subtypes (HPV associated and tobacco-use associated), working with ChIP-seq data from the ENCODE project, or developing software and methods for analysis of deep sequencing of bisulfite modified data. Projects may either be geared towards addressing a biological problem or developing a new method.

Other projects may be available in my lab - see sartorlab.ccmb.med.umich.edu. Feel free to come talk with me if you're interested!

Jieping Ye (Computational Medicine & Bioinformatics)

E-Mail: jpye@med.umich.edu
Website: www.yelab.net

Our project aims to develop novel machine learning and data mining methods to integrate and analyze high-dimensional genomes, connectomes, and multimodal brain images to discover diagnostic and prognostic markers for human brain diseases.

Yang Zhang (Computational Medicine & Bioinformatics)

E-Mail: zhng@umich.edu

  1. Structural prediction and ligand docking of G protein-couple receptors (GPCRs). GPCRs are integral membrane proteins embedded in cell surface and many human diseases involve the malfunction of these receptors. However, experimental solution of GPCR structure has been extremely difficult. This project is to develop computational methods for atomic-level structural modeling of human GPCRs and ligand-receptor interactions.
  2. Protein design. Protein design refers to the effort of designing new protein molecules of a desired 3D structure and function. It is a reversal procedure of protein structure prediction. This project is to develop novel computer methods for automated protein design. The methods are to be applied to a set of important diseases including cancer proteins with experimental validation by our collaborators.
  3. Ligand-protein docking and virtual screening. An important step towards structure-based drug discovery is the structural modeling of ligand-protein binding. However, most of the important drug targets have no experimental structure. This project seeks to develop new ligand-protein docking tools which are suitable for low-resolution protein structures predicted by computer. One aim is to combine the docking tools with protein structure predictions for reliable virtual ligand screening on any interested protein targets.

The projects are supported by National Institutes of Health (NIH R01GM083107 and NIH R01GM084222) and National Science Foundation (NSF DBI0746198).

 

Current Rotations Opportunities 

Center for Computational Medicine and Bioinformatics (CCMB) 

CCMB faculty members may serve mentors for Bioinformatics Program graduate students as well as providing research opportunities for students.

Charles Brooks (Biophysics and Chemistry)

E-mail: brookscl@umich.edu

I have multiple opportunities for rotation students in the lab. These include:
Developing and applying free energy simulation methods to drug discovery and refinement
In this project the student will work with a team on the development of novel free energy simulation methods and analysis techniques that build on both statistical mechanics and foundational methods in modern statistics. Applications will be directed toward the refinement of small molecule inhibitors against protein-based targets, which include HIV-RT, menin-MLL, small molecular transcriptional activators, as well as other protein receptors associated with benchmarking and assessing evolving computational methods.

Novel in silico drug discovery through high-throughput flexible-ligand/flexible-receptor based docking on advanced computing hardware (GPUs)
The focus of this project is in hardening and refining in silico ligand discovery methods that utilize advanced computing platforms, such as GPUs, to achieve high-throughput and scalability in docking screens. Methods development will focus on establishment of optimal protocols for flexible-ligand/flexible-receptor docking as well as the use of machine learning techniques to improving the scoring of docked poses.

Utilizing machine learning algorithms based on auto-encoder/auto-decoder technology for exploration of small molecular and multiple sequence alignment protein sequence property analysis
This project will explore the development of auto-encoder/auto-decoder (AE/AD) machine learning methods to extract and interpolate properties associated with either small molecule collections of drug-like ligands or learning to predict evolutionary trends in proteins from AE/AD based analysis of multiple sequence alignments

Sally Camper (Human Genetics)

E-Mail: scamper@umich.edu

The focus of my laboratory is identifying the molecular basis for congenital birth defects using animal models of human disease. We have three NIH grants and a March of Dimes grant supporting active projects on the development of the neuroendocrine system (pituitary-hypothalamus), auditory system, and axial skeleton. There are at least three rotation projects that are appropriate for bioinformatics students. See the PIBS rotation pages for more details.

Heather Carlson (Medical Chemistry)

E-Mail: carlsonh@umich.edu

The Carlson group focuses on two areas: protein flexibility in computer-based drug design and protein-ligand structural databases. We are developing improved methods for mapping flexible protein surfaces in the drug design project. In the database project, we are mining our Binding MOAD (Mother of All Databases) set to investigate protein flexibility upon binding, amino acid propensities in binding sites, methods for identifying previously unknown binding sites on protein surfaces, and other properties of protein-ligand recognition.

Melissa Duhaime (EEB)

E-Mail: duhaimem@umich.edu

The Duhaime Lab uses (meta)genomics to study the evolution and ecology of ocean viruses, their microbial hosts, and their interactions (i.e., infections) at both the community and single isolate levels. Fall and Winter rotations are available to study viruses of Lake Erie’s toxic algal blooms or Antarctica’s Southern Ocean—with focus on developing novel virus-host prediction algorithms based on both genomic and empirical data. The end goal is the incorporation of network theory to advance our understanding of these microbial predator-prey interactions and their ecosystem-level implications.  Alternatively, students are encouraged to develop their own projects pertaining to viral and microbial genomics or evolutionary/ecological modeling. Please explore http://www-personal.umich.edu/~duhaimem/index.htm for more information..

Oliver He (ULAM)

E-Mail: yongqunh@med.umich.edu

Integrative bioinformatics-based vaccine design
Global public health has dramatically increased due to the successful and effective implementation of immunization programs that utilize major infectious disease vaccines. New vaccines against various infectious diseases (e.g., HIV and tuberculosis) and non-infectious diseases (e.g., cancers and allergies) are also being developed and studied. In the post-genomic era, strategies of vaccine development have progressed dramatically from traditional experiment-to-experiment approaches to bioinformatics-to-experiment approches.

Reverse vaccinology is a cutting-edge vaccine design strategy that starts with bioinformatics analysis of microbial genomes. Dr. He's laboratory has developed Vaxign (http://www.violinet.org/vaxign/), the first web-based vaccine design system based on reverse vaccinology. This pipeline includes prediction of various features, e.g., antigen sublocation, transmembrane domains, adhesin probability, epitope binding to MHC class I and class II, sequence conservation among microbial genomes, and sequence similarities to host proteomics. Vaxign has been proven effective and efficient in vaccine target prediction in many use case applications.

Trachette Jackson (Mathematics)

E-Mail: tjacks@umich.edu

Mathematical Modeling of Endothelial Cell- Tumor Cell Cross Talk

In order to define and quantify the role of VEGF-mediated cross-talk between endothelial and tumor cells on tumor growth dynamics, we would like build two independent, experimentally based mathematical model modules that describe VEGF-mediated upregulation of Bcl-2 in endothelial and tumor cells, respectively. We will then link these modules to understand the impact of the mechanisms by which VEGF orchestrates a dynamic interplay, mediated by Bcl-2, between endothelial cells and tumor cells and to determine the influence of this cross-talk on tumor growth and therapeutic potential.

Required Skills: Basic knowledge of ordinary differential equations and MATLAB; an interest in mathematical/computational modeling

Denise Kirschner (Microbiology and Immunology)

E-Mail: kirschne@umich.edu

We use mathematical and computational modeling tools to study the host-pathogen interaction dynamics for the pathogen Mycobacterium tuberculosis. We are currently focusing on antibiotic treatment and vaccine development. We use many different tools and collaborate with a BSL3 non-human primate center to provide data that guides the development, testing and validation of our work.

Jennifer Linderman (Chemical Engineering)

E-Mail: linderma@umich.edu

The focus of this lab is in developing mathematical and computational models that focus on the role of receptor dynamics and signaling pathways in disease. Particular project: Analysis of simulation data using machine learning tools to identify biological phenotypes relevant to the immune response to M. tuberculosis

Mats Ljungman (Radiation Oncology & Environmental Health Sciences)

E-Mail: ljungman@umich.edu

We have developed a set of new techniques that we call Bru-seq that allows us to obtain very detailed molecular signatures of transcriptional and post-transcriptional regulation in cells. These techniques are based on bromouridine labeling and isolation of nascent RNA to assess genome-wide rates of transcription (Bru-seq), RNA splicing and turnover (BruChase-seq), identification of active enhancer elements (BruUV-seq) and transcription elongation rates (BruDRB-seq). We have generated a large nascent transcriptomic data set and as a newly funded ENCODE mapping center we will generate much more with great opportunities for novel bioinformatics analyses. Potential rotation projects would include:

  1.  Assessing transcriptional and post-transcriptional regulation of cell transitions from fibroblasts into iPSCs and then into neurons
  2.  Transcriptional and post-transcriptional regulation of cellular responses such as TGFb stimulation, heat-shock, hypoxia and DNA damage responses
  3.  Assessing transcription ongoing in repetitive DNA sequences in the genome across multiple cell lines and treatment conditions

David Lubman (Surgery)

E-Mail: dmlubman@umich.edu

Our project involves database searching and processing of archival mass spectral proteomic data to identify the presence of single amino acid variants (SAAVs) which are the equivalent of genomic SNPs. We seek to identify the presence of these SAAVs in cancer stem cells, circulating tumor cells and exosome cargo. Some of the data will compare different clonal areas from different parts of a tumor to study progression of a cancer. We have also recently generated proteomic data on single cells and are interested in the heterogeneity of SAAVs and also of glycosylation of cancer cells. Bioinformatic methods will be used to search and identify these changes. Ultimately, we are interested in how these SAAVs or glycosylations affect the structure of key proteins and are involved in cancer progression.

Rudy Richardson (Toxicology)

E-Mail: rjrich@umich.edu

Current areas of interest for potential research rotations:

  1.  Computational and predictive toxicology. Applying bioinformatics, cheminformatics, QSAR, and molecular modeling (including ligand-receptor docking, inverse docking, homology modeling, and molecular dynamics simulations) to the prediction of toxic effects of chemicals.
  2.  Predicting the structure of neuropathy target esterase (NTE, aka PNPLA6) in order to understand how chemical or genetic modification of its structure leads to neurodegeneration.
  3.  Molecular dynamics simulations aimed at understanding allostery and changes in protein flexibility produced by ligand binding.

Patrick Schloss (Microbiology and Immunology)

E-Mail: pschloss@umich.edu

The Schloss lab develops and tests computational methods for analyzing microbial communities. The goal is to enable researchers to use data generated using next generation sequencing technology to test ecological theory with microbes and better understand how perturbations in these communities affects health. We are looking for curious and creative students interested in the interface between computational biology and microbial ecology.

  1. Analysis of the human microbiome:
  2. Heuristic clustering algorithms for clustering DNA sequences of unknown origin
  3. Development of metatranscriptomic analysis pipeline
  4. Statistical modeling of microbial communities and patient clinical data

Evan Snitkin (Microbiology and Immunology)

E-Mail: esnitkin@umich.edu
Website: thesnitkinlab.com

The Snitkin lab is interested in the application of genomics and bioinformatics approaches to study the evolution and epidemiology of hospital infections. Contact Evan to discuss specific rotation opportunities. In addition, an overview of the labs interests and past publications can be found at: http://thesnitkinlab.com

The types of projects available include:

  1. Mining large sets of healthcare-associated pathogen genomes to characterize the key evolutionary innovations associated with the success of pandemic lineages
  2. Applying phylogenetic approaches to large sets of healthcare-associated pathogen genomes to discern transmission patterns within and between healthcare facilities
  3. Analyzing sequencing data generated directly from patient samples to diagnose diseases of unknown infectious origin
  4. Mining patient health records to identify treatment protocols associated with the evolution of resistance
  5. Applying metabolic modeling approaches to make predictions regarding how GI pathogens colonize the host and compete with commensals
  6. Applying short-read sequencing approaches to characterize the genetic diversity of pathogen populations within individual patients

Chandra Sripada (Psychiatry)

My lab is uses functional neuroimaging to tackle the biomarker problem in psychiatry: the problem of constructing objective, quantitative measures for psychiatric disorders and clinically-relevant personality dimensions. Much of our recent work identifies graphical structure in “functional connectomes,” which are whole-brain maps of connectivity across thousands of brain regions. Students have opportunities to develop new analytic methods to quantify change in graphical structure over time (working with our collaborators in EECS and Statistics). We intend to use these methods to characterize aberrant change patterns in disordered populations, including adults with schizophrenia and children with attention dysfunction.

Muneesh Tewari (Biomedical Engineering/Internal Medicine)

E-mail: mtewari@umich.edu
Website: www.tewarilab.org

The Tewari lab is developing and testing next generation approaches for multi-dimensional monitoring of health and early detection of diseases. This includes biomarker analyses using cell-free DNA, RNA, and other analytes in biofluids like blood and urine, as well as highly time resolved data obtained from wearable sensors and clinical data.

We are an interdisciplinary lab that collaborates with clinicians, chemists and engineers, biostatisticians, computational and data scientists and others. Dr. Tewari has an eclectic background including systems and quantitative biology, cell and molecular biology, clinical medicine (with a specialization in medical oncology), and is a technology enthusiast.

Rotation projects are available involving analysis of physiologic data from wearable sensors and other time-resolved data sources, as well as bioinformatic analysis of next generation sequencing data.

We are looking for students who are inspired, pro-active, and interested in inter-disciplinary research. A strong computational background is needed because we are not primarily a computational lab. As we are actively promoting a growth culture, an interest in self-assessment and self-development is also important to be a good fit for the lab. We offer an environment and research work that can enable training and experiences across disciplines and interaction with diverse types of collaborators.

Scott Tomlins (Pathology)

E-Mail: tomlinss@umich.edu

Our lab uses next generation sequencing to profile the cancer genome and transcriptome with a focus on preciion medicine.

We focus on assessing routine tissue samples from patients with cancers from diverse organs using Ion Torrent instrumentation in our laboratory.

Rotations are available to work in a range of bioinformatics areas related to precision medicine from primary data analysis to clinical implementation.

Specific rotation projects including developing novel error models to minimize false positive/negative variant and copy number calls, developing methodology to automate data visualization and prioritize drivers, and integrate DNA and RNA based alterations from large cohorts to make biological insights."

Nils Walter (Chemistry)

E-Mail: nwalter@umich.edu

We have a diverse set of projects available that use bioinformatics, computational biophysics, systems biology and kinetic modeling approaches to interpret single molecule fluorescence microscopy data that illuminate how the recently discovered, ubiquitous universe of non-protein coding RNAs drives all aspects of gene expression and regulation in eukaryotes. Applications range from basic studies of RNA catalysis and interference, pre-mRNA splicing, and mRNA translation to understanding the onset of cancer in misregulated human cell lines. Here is a brief outline of possible rotation projects:

  1. Use bioinformatics and clustering to analyze complex single molecule signal traces
  2. Use atomistic molecular dynamics and coarse-grained simulations to understand the coupling of local and global motions in RNA enzymes
  3. Use Monte-Carlo simulations to understand complex diffusive behaviors of single molecules and nanodevices
  4. Use systems biology modeling to integrate vast datasets into mechanistic models of important cellular processes

Shaomeng Wang (Medicine, Pharmacology and Medicinal Chemistry)

E-Mail: shaomeng@med.umich.edu
Website: sw16.im.med.umich.edu

Potential projects include:

  1. Deriving gene-signatures for predicting anticancer activity of novel drugs developed in our lab to guide future clinical trials.
  2. Developing new computational and bioinformatics tools and methods for drug design;
  3. Computational structure-based drug design.

Andrzej Wierzbicki (MCDB)

E-Mail: wierzbic@umich.edu
Website: labs.mcdb.lsa.umich.edu/labs/wierzbicki

Our lab is focused on understanding non-coding regions of the genomes. We study how RNA produced from non-coding sequences (non-coding RNA) controls genome activity on the chromatin level. Chromatin-level gene regulation includes DNA methylation, histone modifications, nucleosome positioning and three-dimensional organization of chromosomes. We study these processes using genomic approaches and in depth bioinformatic analysis to gain mechanistic and quantitative understanding of genome regulation. Our work may be described as an interface of RNA biology and epigenomics.

Graduate students rotating in the lab would have the opportunity to work in one of the two following projects:

  1. Resolve the molecular mechanisms used by non-coding RNA to control chromatin structure. This project, funded by a recently awarded NIH grant, involves studying nucleosome positioning and higher level chromatin organization in various mutant backgrounds defective in non-coding RNA production and processing. This project involves establishment and application of a bioinformatic toolset suitable for high quality analysis of genome-wide nucleosome positioning data.
  2. Test if structures of non-coding RNA affect their functions and if these structures are actively modulated during RNA-mediated processes. This project, funded by an NSF grant, involves establishment of a toolset for genome-wide structural assays of non-coding RNA structures.

Qiong Yang (Biophysics)

E-Mail: qiongy@umich.edu

The Yang Lab studies biological oscillations and self-organization processes in cell-free systems and early zebrafish embryos. The local interactions in the form of mechanical and biochemical signals allow individual molecules and cells to generate collective spatiotemporal patterns. To pin down the physical mechanisms behind these processes, we integrate mathematical modeling, live-cell and super-resolution imaging, and microfluidics to study both water-in-oil droplet-based artificial cells and live embryos, and connect the understandings across the molecular, cellular, and embryonic levels. We look forward to recruiting students with a quantitative background and a strong interest in interdisciplinary research. The position is immediately available and the starting date is flexible. How to apply: Interested candidates should send a brief description of your interest and CV to Email: qiongy@umich.edu. Dr. Qiong Yang.

Below are two current major research efforts in lab:

  1. Emergent phenomena in biological systems
    Investigating how self-organization behaviors, such as mitotic trigger waves in artificial cell-free systems and somite pattern formation in embryos, arise from complex interactive networks of cells and molecules through biochemical signals and mechanical forces.
  2. Method development for quantitative biology
    Development of an integrated interdisciplinary approach to study biological clock design, function, and coordination, e.g. statistical techniques to identify network motifs for clock function, combination of modeling, fluorescence imaging, and microfluidics, to quantitatively manipulate and analyze the oscillatory processes in artificial mitotic cells, live tissues and zebrafish embryos.

Jianzhi George Zhang (EEB)

E-Mail: jianzhi@umich.edu

Rotation options for evolutionary genetics, genomics and systems biology are available in my lab. They can be either experimental or computational. The experimental work is typically done in budding yeast. Current experimental and computational projects focus on position effects on gene expression level and noise, genome organization and 3D chromosome conformation, recombination rate variation, epistasis, pleiotropy, phenotypic plasticity, fitness landscape, and post-transcriptional modification, all in the context of evolution. I also encourage students to develop their own projects in the general area of evolutionary genetics/genomics. More information found at www.umich.edu/~zhanglab/index.html.

Xiang Zhou (Biostatistics)

E-Mail: xzhousph@umich.edu
Website: www.zhoulab.org

Rotation opportunity is currently available in Dr. Xiang Zhou's lab in the Department of Biostatistics. The Zhou Lab is focused on developing statistical and computational methods to address interesting biological problems in genetic and genomic studies. These studies often involve large-scale and high-dimensional data sets, and examples include genome-wide association studies and functional genomic sequencing studies (RNAseq, ChIPseq etc.). Through developing novel analytic methods to extract important information from these data, we hope to advance our understanding of the genetic basis of phenotypic variation for various quantitative traits and complex diseases. Please refer to the website (www.zhoulab.org) for more details. Current research projects include developing statistical methods for association tests with multiple correlated phenotypes, for integrating functional genomic studies with genome-wide association studies, for phenotype/risk prediction, for epistasis contribution and heritability estimation, and Bayesian methods for big data sets. Please contact Dr. Xiang Zhou (xzhousph@umich.edu) if you are interested.