2014-15: Bioinformatics: Statistical Modeling and Analysis of Whole Genome Methylation and Chromatin Interaction (Epigenetics): March 9-10, 2015

Workshop Information

March 9, 2015 - 8:30am - March 10, 2015 - 2:00pm

Schedule
Participant List
Speaker Titles and Abstracts
Posters

This workshop was held at SAMSI in Research Triangle Park, NC.

Description

Methylation is the cornerstone of epigenetics. With the next generation sequencing (NGS) technology, whole genome nucleotide resolution methylation data (NRMD) are increasingly available. However, small sample size, correlation between CpG sites, and large variability in the signals, all present difficulties in detecting differentially methylated regions. Although there are a few statistical methods proposed for analyzing such data to date, there are still many unanswered questions. To complicate matter further, a mapping is required to infer NRMD for a cost-effective methylation detection technology, but statistical models for accomplishing this task are lacking. Another area of epigenetics that has gained a great deal of attention in recent years is the spatial organization of genome and regulation. Recent NGS-aided technologies, such as Hi-C and ChIA-PET, have led to the generation of genome-scale chromatin interaction data, which made it possible to recapitulate 3D chromatin structure and detect spatial interactions between important proteins and their target genes. These big data pose a number of challenging statistical issues, including "random collisions" (false positives), highly correlated data due to many-to-many mappings, over-dispersion, and very large dimensionality of the parameter space for reconstructing 3D structures. A number of statistical and computational tools have been proposed, but a great deal is yet to be done for the statistical community to make an impact in these emerging areas of epigenetics. Most importantly, statistical methods proposed need to be completely in sync with pressing biological issues being addressed in the scientific community.

This workshop aimed to (1) introduce participants at all levels (from graduate students, to postdocs, to junior and senior faculty in academic institutions) and backgrounds (biological, computational, and statistical) to current state-of-the-art genomic technology and research in statistical methods for these two areas of epigenetics, (2) create a forum for generation and discussion of ideas for tackling the challenges in analyzing methylation and chromatin interaction data, and (3) build a bridge for new, and strengthen existing, collaboration among participants.

Participants could optionally submit an abstract for a short presentation at the Poster session on Monday (March 9th, 2015) evening. A small subset of the submitted abstracts were selected for short presentations at the workshop. Abstracts for presentation at the workshop: Oral or a poster presentation. If submitted, but not selected, for an oral presentation, the author may still present it as a poster.

SAMSI Directorate Liaison: Sujit Ghosh

If you have any questions please send email to [email protected]

Schedule

Monday, March 9, 2015
at SAMSI

8:00 a.m. Shuttle to SAMSI
8:30-8:50 a.m. Registration
8:50-9:00 Introduction and Welcome
Sujit K. Ghosh, SAMSI and Shili Lin, Ohio State University
9:00-10:30 Session 1: Epigenetics and Statistical Methods for Analyzing Epigenetic Data
Chair: Shili Lin, Ohio State University
  Bob Schmitz, University of Georgia
Challenges and Biases Associated with Whole-Genome Bisulfite Sequencing Data
  Michael Zhang, University of Texas, Dallas
Computational Advances in ChIP-seq and ChIA-PET Data Analysis
10:30-11:00 Break
11:00-12:30 Session 2: DNA Methylation I
Chair: Yong Seok Park, University of Pittsburgh
  Peng Jin, Emory University
Dynamic Cytosine Modifcation in Human Diseases
  Maureen Sartor, University of Michigan
Analysis Tool for Combined DNA Methylation and 5-Hydroxymethylcytosine Data
  Hao Wu, Emory University
Differential Methylation Analysis from Whole Genome Bisulfite Sequencing: a Matter of Spatial Correlation, Coverage Dept, and Biological Variance
12:30-2:00 Lunch
2:00-3:00 Session 3: Modeling of Long-range Chromatin Interaction I
Chair: Ming Hu, New York University
  Inkyung Jung, University of California, San Diego
Deciphering Dynamic Chromatin 3D Organization: from Structure to Gene Regulation
  Liang Niu, University of Cincinnati
Statistical Modeling and Analysis of ChIA-PET Data
3:00-3:30 Break
3:30-5:00 Session 4: Contributed talks (4 20-minute talks)
Chair: Victor Jin, University of Texas, San Antonio Health Science Center
  Erick Lock, University of Minnesota
Bayesian Screening for Group Differences in Methylation Array Data
  Deepak Ayyala, Ohio State University
Faster and Efficient Tests for Detection of Differentially Methylated Region from MethylCap-seq Data
  Oswaldo Lozoya, NIH/NIEHS
The Impact of Mitochondrial Dysfunction on the Epigenome
  Chenchen Zou, Jackson Laboratory for Genomic Medicine
Multi-track Structure Inference Model for Genome-wide Chromatin Conformation-capturing Data
5:00-7:00 Poster Session and Reception (SAMSI, 2nd floor Commons)

SAMSI will provide poster presentation boards and tape. The board dimensions are 4 ft. wide by 3 ft. high. They are tri-fold with each side being 1 ft. wide and the center 2 ft. wide. Please make sure your poster fits the board. The boards can accommodate up to 16 pages of paper measuring 8.5 inches by 11 inches.
7:00 Shuttle to Hotel

Tuesday, March 10, 2015
at SAMSI

8:00 a.m. Shuttle to SAMSI
8:45-9:00 a.m. Registration and Announcements
Shili Lin, Ohio State University
9:00-10:30 Session 5: DNA Methylation II
Chair: Steve Qin, Emory University
  Pearlly Yan, Ohio State University
DNA Methylation Profiling in Cancer: Perspectives from a Genomics/Computation Group
  Yong Seok Park, University of Pittsburgh
Statistical Analysis of DNA Methylation using Within-Fragment Information
  Karen Conneely, Emory University
DNA Methylation, Gene Expression, and Aging: what Can We Learn from Cross-Sectional Microarray Data?
10:30-11:00 Break
11:00-12:30 Session 6: Modeling of Long-Range Chromatin Interaction II
Chair: Hao Wu, Emory University
  Miriam Huntley, Harvard University
How the 3D Genome Folds - Now in the Loop
  Ming Hu, New York University
A Hidden Markov Random Field Based Bayesian Method for the Detection of Long-Range Chromosomal Interactions in Hi-C Data
  Victor Jin, Univ. of Texas, San Antonio Health Science Center
Genomic Analysis of Three-Dimensional Data Identifies Functional Enhancer-Mediated Looping
12:30-2:00 Lunch and Adjourn