Computational Genomics Summer Institute 2019

The 2019 UCLA Computational Genomics Summer Institute.CGSI brings together mathematical and computational scientists, sequencing technology developers in both industry and academia, and the biologists who use the instruments for particular research applications. Research talks, workshops, journal clubs, and social events provide a unique opportunity to foster interactions between these three communities over an extended period of time and advance the mathematical foundations of this exciting field.

DATES
SHORT PROGRAM #1: July 15 – 19, 2019
SHORT PROGRAM #2: July 29 – August 2, 2019
LONG PROGRAM: July 10 – August 2, 2019

@ UCLA Campus, Los Angeles
Visit our website to learn more: CGSI 2019
Check out the schedule from last year: CGSI 2018

The application is open now!
Apply now for this upcoming summer’s Short and Long Courses:
STEP #1 APPLY
STEP #2 SEND YOUR CV to uclacgsi@gmail.com

The regular registration deadline to apply for the 2019 programs is March 1st, 2019.
Overview
In 2015, Profs. Eleazar Eskin (UCLA), Eran Halperin (UCLA), John Novembre (The University of Chicago), and Ben Raphael (Brown University) created the Computational Genomics Summer Institute (CGSI). A collaboration with the Institute for Pure and Applied Mathematics (IPAM), CGSI aims to build a community focused on methods development in Bioinformatics.

The 2019 CGSI Organizers

CGSI Program Co-directors:
Eleazar Eskin, UCLA
Eran Halperin, UCLA
Dima Shlyakhtenko, UCLA IPAM

CGSI Organizing Committee:
Jessica (Jingyi) Li, UCLA
Sriram Sankararaman, UCLA
David Koslicki, Oregon State University
Eran Halperin, UCLA
Eleazar Eskin, UCLA

The 2016, 2017 and 2018 programs were a huge success – we hope you will be a part of the program this summer!
You can see our 2018 schedule with the videos here.

Social Programs from previous years includes:
Concert at the Hollywood Bowl
Bike rides along the Pacific Coast
Retreat in the Mountains

2019 Faculty
(Additional faculty will be added in the next few months)
Can Alkan, Bilkent University
David Anastasiu, San Jose State University
Valerie Arboleda, UCLA
Sharon Aviran, UC Davis
Vineet Bafna, UCSD
Lisa Bastarache, Vanderbilt University
Dan Benjamin, USC
Gillian Belbin, Icahn School of Medicine at Mount Sinai
Ran Blekhman, University of Minnesota
Paul Boutros, UCLA
Na Cai, EBI
Shai Carmi, The Hebrew University of Jerusalem
Rayan Chikhi, CNRS
Karen Conneely, Emory University
Nancy Cox, Vanderbilt University
Jason Ernst, UCLA
Eleazar Eskin, UCLA
Jonathan Flint, UCLA
Nandita Garud, UCLA
Simon Gravel, McGill University
Eran Halperin, UCLA
Jo Hardin, Pomona College
Fereydoun Hormozdiari, UC Davis
Haky (Hae Kyung) Im, University of Chicago
Iuliana Ionita, Columbia University
Hyun Min Kang, University of Michigan
Eimear Kenny, Icahn School of Medicine at Mount Sinai
David Koslicki, Oregon State University
Smita Krishnaswamy, Yale University
Jessica (Jingyi) Li, UCLA
Jian Ma, CMU
Anna Spafo Malaspina, SIB
Jonathan Marchini, Regeneron Genetics Center
Siavash Mir Arabbaygi, UCSD
Quaid Morris, University of Toronto
Magnus Nordborg, GMI, Austria
John Novembre, University of Chicago
Layla Oesper, Carleton College
Bogdan Pasaniuc, UCLA
Ben Raphael, Princeton University
Saharon Rosset, Tel Aviv University
Sushmita Roy, WID
Cenk Sahinalp, Indiana University Bloomington
Sriram Sankararaman, UCLA
Michael Schatz, Johns Hopkins University
Alexander Schönhuth, CWI, Amsterdam
Sagiv Shifman, The Hebrew University of Jerusalem
Sagi Snir, University of Haifa
Jae-Hoon Sul, UCLA
Fabio Vandin, University of Padova
Peter Vischer, University of Queensland, Australia
Naomi Wray, University of Queensland, Australia
Yi Xing, UCLA
Alex Zelikovsky, Georgia State University
James Zou, Stanford University
Or Zuk, Hebrew University

Reference-free comparison of microbial communities via de Bruijn graphs

Microbial communities inhabiting the human body exhibit significant variability across different individuals and tissues and are likely play an important role in health and disease. Serghei Mangul and David Koslicki (Oregon State University) recently published a paper presenting a novel approach for characterizing microbial communities in metatranscriptomics studies. Koslicki developed this tool, which may help scientists explore the role microbiota play in disease development, especially when comparing microbiomes of healthy and disease subjects.

Identifying and characterizing the relative abundance of microbiota in different tissues is essential to better understanding the role of microbial communities in human health. Current approaches use reference databases to identify, classify, and compare microbial communities present in the individual host. However, existing databases are incomplete and rely on a limited compendium of reference genomes. Current reference-based approaches are unable to accurately determine microbial compositions to the extent that could be possible given the high resolution of data produced by today’s high throughput sequencing technology.

Framework of the study. For more information, download our paper.

Ideally, comparison of microbial communities across samples could circumvent this limiting classification step. Mangul and Koslicki recently developed EMDeBruijn, a reference-free approach that uses all available non-host microbial reads, not just those classified in reference databases, to compare microbial communities.

First, EMDeBruijn translates sequencing data to a de Bruijn graph, which represents overlaps between symbols in sequences. De Bruijn graphs are commonly used in de novo assembly of short read sequences to a genome, but have not yet been applied in a reference-free approach. EMDeBruijn then uses properties of the de Bruijn graphs to compare microbiome composition across individuals. This metric is reduced using the Earth Mover’s Distance (EMD), a statistic that can measure the distance between two probability distributions over a region.

In their recent paper, Mangul and Koslicki applied EMDeBruijn to study the composition and abundance levels of the microbial communities present in blood samples from coronary artery calcification (CAC) patients and controls. EMDeBruijn uses candidate microbial reads to differentiate between case (CAC-affected) and control (healthy) samples, and a filtered set of non-host reads are used to determine the composition of the blood microbiome. Hierarchical clustering using the EMDeBruijn metric successfully identifies several large clusters unique to samples from either health or control groups.

This study indicates the presence of the disease-specific microbial community structure in CAC patients, and points to the need for additional investigation of potentially causal relationships between the microbiome and CAC disease.

Using the same data set, Mangul and Koslicki compare the results of EMDeBruijn with those of current approaches. Existing computational methods, including MetaPhlAn and RDP’s NBC, discovered various microbial communities across the health and control samples. However, neither of these methods were able to identify any disease-specific patterns in the microbiome nor discriminate the samples into disease and healthy groups.

EMDeBruijn provides a powerful, species independent way to assess microbial diversity across individuals and subjects. For more information, see our paper, which was published in the Proceedings of the 7th ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics: http://dl.acm.org/citation.cfm?id=2975174.

Code implementing this method is available at: https://github.com/dkoslicki/EMDeBruijn.

Visualization of the EMDeBruijn Distance. a) Pictorial representation of 2-mer frequencies for two hypothetical samples, S1 and S2. b) The 2-mer frequencies overlaid the de Bruijn graph B2(A ). c) Representation of the flow used to compute EMD2(S1; S2); dark arrows denote mass moved from the initial node to the terminal node. d) Result of applying the flow to the 2-mer frequencies of S1.

This project was a collaboration that started at the Mathematical and Computational Approaches in High-Throughput Genomics program held in Fall 2011 at the Institute of Pure and Applied Mathematics (IPAM). Our on-going Computational Genomics Summer Institute (CGSI; also co-organized by IPAM) was inspired by the 2011 program. Check out the 2017 CGSI website for a preview of this summer’s programs – the deadline for applications is February 1, 2017!

The full citation to our paper is:

Mangul S, Koslicki D. Reference-free comparison of microbial communities via de Bruijn graphs. In Proceedings of the 7th ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics. 2016 Oct 2 (pp. 68-77). Association for Computing Machinery, New York.

UCLA Bioinformatics: The Philosophy of the Training Environment and Programs

(This post is jointly authored with Alexander Hoffmann, Hilary Coller, Matteo Pellegrini, and Nelson Freimer.)

UCLA has a rich training environment for Bioinformatics that extends beyond the core academic programs.  For structured academic learning, UCLA offers an Undergraduate Bioinformatics Minor and a Bioinformatics Ph.D. Program.  In addition, UCLA coordinates multiple training programs, several of which are open to researchers from other institutions who are at all stages of their careers.  Many of these programs are either hosted or jointly sponsored by the Institute for Quantitative and Computational Biology (QCB) at UCLA, which is directed by Alexander Hoffmann (UCLA).

Over the past 10 years, driven by the ubiquity of genomics throughout the field, biology has become a data science. Every biomedical research institution has been challenged with supporting the analysis of genomic data generated by groups who traditionally have not cultivated substantial computational expertise. Many of our peer institutions delegate genomic data analyses to a specific Bioinformatics core group that operates on a “fee-for-service” model.

The Bioinformatics core “fee-for-service” model poses many problems.  First, complex issues that arise during analysis of genomic data are difficult to predict in advance.  Projects often require much more effort than anticipated by research groups, leading core groups to struggle with insufficient funds to cover the actual time spent on analysis.  Second, research groups utilizing the core often want to move the project in different directions than what was originally proposed.  In the long term, exploring additional aspects of data can be inefficient when data analysis is delegated to a core group on an as-needed basis.

At UCLA we follow a different approach.  We believe that research groups should receive the training and resources to analyze the genomic data that they generate.  This “training and collaboration” model is the best solution for efficiently completing projects and advancing skills in a research group.  Over the past ten years, UCLA has significantly invested in this training and collaboration model.  For example, UCLA’s Bioinformatics programs are explicitly organized to connect research groups with core groups across campus and provide infrastructure and training to students, faculty, and staff working in many different fields.

Bioinformatics training programs held at UCLA include:

    1. The Collaboratory. The Collaboratory of postdoctoral fellows, directed by Matteo Pellegrini (UCLA), provides an experimental and empirical research environment for bioscientists and computational scientists to collaboratively design and conduct experiments. Most bioscience laboratories have limited capabilities in large-scale data analysis. The Collaboratory’s main mission is to advance genomic data analysis by connecting UCLA bioscience faculty with QCB faculty and fellows.  The Collaboratory fellows are a select group of postdocs funded by the Collaboratory to engage in collaborative projects that leverage their specific expertise.

      The Collaboratory fellows are also responsible for organizing intensive tutorials designed to train UCLA students and postdocs in the latest next-generation sequence analysis techniques. In addition to providing computational expertise to bioscience researchers at UCLA, the Collaboratory also sets up and maintains a next-generation sequence data analysis server, and participants develop methodologies to process new types of data. The Collaboratory has a year-round schedule of workshops open to the Bioinformatics community.

 

    1. Bruins in Genomics Undergraduate Summer Research Program (B.I.G. Summer). B.I.G. Summer is an integrated undergraduate training and research program in genomics and bioinformatics at UCLA. Participants gain an intensive, practical experience in integrating quantitative and biological knowledge while learning how to pursue graduate degrees in the biological, biomedical or health sciences.  The program begins with two weeks of hands-on tutorial workshops that cover fundamental concepts in genomics critical to participation in today’s research.  The remaining weeks are focused on research.  Students work in pairs under the supervision of UCLA faculty mentors and QCB postdoctoral fellows.

      B.I.G. Summer offers unique opportunities that are often not available to undergraduates, including next generation sequencing analysis workshops, weekly science talks by senior researchers, a weekly journal club, professional development seminars, social activities, concluding poster sessions, and a GRE test prep course.  In addition, a special NIH-funded curriculum in neurogenomics, directed by Nelson Freimer and Eleazar Eskin, provides B.I.G. Summer participants with an intensive exposure to this rapidly growing field, in which UCLA is among the leading centers worldwide. B.I.G. Summer is organized by Alexander Hoffmann, Hilary Coller, Tracy Johnson, and Eleazar Eskin. This year, B.I.G. Summer is held from June 19th to August 11th, 2017.  The B.I.G. Summer Program is sponsored by the following generous institutions:

      UCOP for a UC-HBCU partnership Program in Genomics and Systems
      NIH NIBIB for NGS Data Analysis Skills for the Biosciences Pipeline R25EB022364
      NIH NIMH for Undergraduate Research Experience in Neuropsychiatric Genomics R25MH109172

 

    1. Undergraduate and MS Research Program. One of the best ways for faculty to provide training to undergraduate and graduate students is through mentorship in research labs. A substantial challenge to this approach is the increasing number of undergraduate students who want to get involved in research.  For example, there are many more Computer Science majors interested in research than can be absorbed by the number of faculty presently in the Department of Computer Science.  In order to meet rising undergraduate demand for research opportunities, we created an Undergraduate and Master’s student research program.

      This program connects researchers across campus with interested students from a variety of majors.  In doing so, we leverage UCLA’s strength in Bioinformatics to offer a greater number of research opportunities available to undergraduates with and outside of the Department of Computer Science.  Each research opportunity posted on the webpage has a list of requirements, ranging from “one course in Bioinformatics or programming” to “a full year of coursework in programming.”  For students who have completed relevant coursework or are planning their academic schedule, this program provides a clearly defined path to become involved in research projects on campus.

 

    1. Informatics Center for Neurogenetics and Neurogenomics (ICNN). As with other areas of biomedical science, the post-genome era raises the prospect of transformational advances in neuroscience research. However, neuroscience faces special challenges in analysis, interpretation, and management of the vast quantities of information generated by genetic and genomic technologies. The phenotypic and organizational complexity of the nervous system calls for distinct analytical and informatics strategies and expertise.

      The ICNN, directed by Nelson Freimer and Giovanni Coppola, provides advanced analysis and informatics support to a highly interactive group of neuroscientists at UCLA who conduct basic, clinical, and translational research.  Generally, today’s lack of corresponding resources in analysis and informatics constitutes a bottleneck in their research; ICNN provides for these investigators access to excellent facilities for genetics and genomics experimentation.  ICNN faculty are experts in statistical genetics, gene expression analysis, and bioinformatics, and they oversee the activities of highly-trained staff members in  accomplishing three goals: (1) Providing expert consultation and analyses for neurogenetics and neurogenomics projects;  (2) Developing and maintaining a shared computing resource that is incorporated within the large campus-wide computational cluster for computation-intensive analyses, web-servers, and state of the art software tools for a wide range of applications (including user-friendly versions of public databases, as well as workstations on which ICNN users will be trained to employ these tools); (3) Providing hands-on training in analysis and informatics to group users.

 

  1. Computational Genomics Summer Institute (CGSI). In 2015, Profs. Eleazar Eskin (UCLA), Eran Halperin (UCLA), John Novembre (The University of Chicago), and Ben Raphael (Princeton University) created CGSI. A collaboration with the Institute for Pure and Applied Mathematics (IPAM), led by Russ Caflisch, CGSI is developing a flexible program for improving education and enhancing collaboration in Bioinformatics research. The goal of this summer research program is to bring together mathematical and computational scientists, sequencing technology developers in both industry and academia, and the biologists who use the instruments for particular research applications.

    CGSI is a unique opportunity for junior and senior scholars in Bioinformatics to foster collaborative relationships, accelerate problem-solving, and unleash the full potential of their projects.  The program facilitates interdisciplinary collaboration and training with a mix of formal and informal events. For example, senior scholars present traditional research talks and tutorials, while junior scholars present mini-presentations and organize journal clubs.  CGSI fosters interactions over an extended period of time and is laying crucial groundwork to advance the mathematical foundations of this exciting field.  This year, CGSI will be held from July 6th-26th, 2017. CGSI is made possible by National Institutes of Health grant GM112625.

 

“Give a Man a Fish, and You Feed Him for a Day. Teach a Man to Fish, and You Feed Him for a Lifetime.”