Bioinformatics for genomics Kickoff Bioinformatics Expertise Center 10 November 2009 Judith Boer Dept. of Human Genetics.

Slides:



Advertisements
Similar presentations
CD40 ligand and tumor necro sis factor alpha, the cells acquire a mature phenotype of dendritic cells that is characterized by up-regulation of human leukocy.
Advertisements

High throughput sequencing Barbera van Schaik
The journal as index and incentive for data publication Myles Axton Editor, Nature Genetics Cambridge Oct 23 rd 2011.
Introduction to BioConductor Friday 23th nov 2007 Ståle Nygård Statistical methods and bioinformatics for the analysis of microarray.
Basic Genomic Characteristic  AIM: to collect as much general information as possible about your gene: Nucleotide sequence Databases ○ NCBI GenBank ○
Bioinformatics at WSU Matt Settles Bioinformatics Core Washington State University Wednesday, April 23, 2008 WSU Linux User Group (LUG)‏
Next-generation sequencing and PBRC. Next Generation Sequencer Applications DeNovo Sequencing Resequencing, Comparative Genomics Global SNP Analysis Gene.
Genome Browsers Ensembl (EBI, UK) and UCSC (Santa Cruz, California)
Visualization of genomic data Genome browsers. UCSC browser Ensembl browser Others ? Survey.
Aleksi Kallio CSC – IT Center for Science Chipster and collaboration with other bioinformatics platforms.
Data retrieval BioMart Data sets on ftp site MySQL queries of databases Perl API access to databases Export View.
Presented by Karen Xu. Introduction Cancer is commonly referred to as the “disease of the genes” Cancer may be favored by genetic predisposition, but.
Diabetes and Endocrinology Research Center The BCM Microarray Core Facility: Closing the Next Generation Gap Alina Raza 1, Mylinh Hoang 1, Gayan De Silva.
341: Introduction to Bioinformatics Dr. Natasa Przulj Deaprtment of Computing Imperial College London
Login: BITseminar Pass: BITseminar2011 Login: BITseminar Pass: BITseminar2011.
What is Bioinformatics?. Conceptualizing biology in terms of molecules and then applying “informatics” techniques from math, computer science, and statistics.
SIGMA: A Platform to Visualize and Analyze DNA Copy Number Microarray Data Raj Chari, PhD Student BC Cancer Research Centre Department of Cancer Genetics.
Quality assessment AATGCGTACATGCACCANTTCAG GTC TGTCANNTGCATTACATGCATTGA CC AATGCGTACATGCACCANTTCAG GTC TGTCTTTTGCATNACATGCAAAAA CC TGTCTTTTGCATNACATGCAGGG.
Bioinformatics Core Facility Ernesto Lowy February 2012.
Databases in Bioinformatics and Systems Biology Carsten O. Daub Omics Science Center RIKEN, Japan May 2008.
Analysis of Microarray Data 1.Scan the images 2.Quantify intensity of spots 3.Normalization 4.Analysis of data 5.Identification of genes of interest 6.Validation.
Detecting enriched regions (Chip- seq, RIP-seq) Statistical evaluation of enriched regions Data displayed in Genome Browser Detection of enriched motifs.
01/03/2013UK NEQAS UV Participants Meeting 2013 in a quality perspective.
The Center for Medical Genomics facilitates cutting-edge research with state-of-the-art genomic technologies for studying gene expression and genetics,
ELIXIR UK - Industry Engagement sector Gabriella Rustici School of Biological Sciences.
UCSC Genome Browser 1. The Progress 2 Database and Tool Explosion : 230 databases and tools 1996 : first annual compilation of databases and tools.
Next Generation Sequencing and its data analysis challenges Background Alignment and Assembly Applications Genome Epigenome Transcriptome.
Practically Genomic A hands-on bioinformatics IAP Course Materials: Instructors: Paola Favaretto, Sebastian Hoersch,
© 2004 by Genomatix Software GmbH Genomatix Dr. Martin Seifert Genomatix Software GmbH Landsberger Strasse 6, D München
EDACC Primary Analysis Pipelines Cristian Coarfa Bioinformatics Research Laboratory Molecular and Human Genetics.
David R. McWilliams, Ph.D. Section of Statistical Genetics, Department of Biostatistical Sciences, Center for Public Health Genomics Bioinformatician IV.
Korea BioInformation Center Byoung-Chul Kim
Browsing the Genome Using Genome Browsers to Visualize and Mine Data.
3/24/2005 TIGP 1 Bioinformatics for Microarray Studies at IBS Pei-Ing Hwang, Ph.D. Mar. 24, 2005.
Next Generation Sequencing pipeline: a joint LONI – BIRN [UCLA – UCI] collaborative project F. Macciardi – March 16, 2011.
Bioinformatics Core Facility Guglielmo Roma January 2011.
NextGen Pipeline: Enabling the Plant Science Community Tom Brutnell (lead), Steve Rounsley (co-lead), Matt Vaughn (Engagement Lead) Ed Buckler, Justin.
Sackler Medical School
Analysis of GEO datasets using GEO2R Parthav Jailwala CCR Collaborative Bioinformatics Resource CCR/NCI/NIH.
RNA-Seq Primer Understanding the RNA-Seq evidence tracks on the GEP UCSC Genome Browser Wilson Leung08/2014.
Bioinformatics Curriculum Issues, goals, curriculum.
Bioinformatics lectures at Rice University Li Zhang Lecture 11: Networks and integrative genomic analysis-3 Genomic data
1 Bioinformatics at Norwegian University of Science and Technology Professor Finn Drabløs Department of Cancer Research and Molecular Medicine Finn Drabløs.
Analyzing digital gene expression data in Galaxy Supervisors: Peter-Bram A.C. ’t Hoen Kostas Karasavvas Students: Ilya Kurochkin Ivan Rusinov.
Data Integration & Data Mining Tool Donald Dunbar BHF CoRE Bioinformatics Team Edinburgh Bioinformatics Meeting April 2013.
No reference available
__________________________________________________________________________________________________ Fall 2015GCBA 815 __________________________________________________________________________________________________.
Current Data And Future Analysis Thomas Wieland, Thomas Schwarzmayr and Tim M Strom Helmholtz Zentrum München Institute of Human Genetics Geneva, 16/04/12.
Accessing and visualizing genomics data
Affymetrix User’s Group Meeting Boston, MA May 2005 Keynote Topics: 1. Human genome annotations: emergence of non-coding transcripts -tiling arrays: study.
Visualization of genomic data Genome browsers. UCSC browser Ensembl browser Others ? Survey.
Discriminating somatic and germline mutations in tumour DNA samples without matching normals Saskia Hiltemann Erasmus Medical Center, Rotterdam MGC Symposium,
Using public resources to understand associations Dr Luke Jostins Wellcome Trust Advanced Courses; Genomic Epidemiology in Africa, 21 st – 26 th June 2015.
Microarray Technology and Data Analysis Roy Williams PhD Sanford | Burnham Medical Research Institute.
High Throughput Sequence (HTS) data analysis 1.Storage and retrieving of HTS data. 2.Representation of HTS data. 3.Visualization of HTS data. 4.Discovering.
Practice:submit the ChIP_Streamline.pbs 1.Replace with your 2.Make sure the.fastq files are in your GMS6014 directory.
Ingenuity Pathway Analysis Alex Pico. Description "IPA is a software application that enables researchers to analyze and understand the complex biological.
Bioinformatics Educated by Zhenglin Zhu School of Life Sciences, Chongqing U.
Preparing published variants with Mutalyzer webservices Gerard C.P. Schaafsma Department of Human Genetics.
? ? Individual 1Individual 2 1. Questions This is a pedigree for a disease involving a mutation within an imprinted gene. The disease manifests only when.
How to get from a pile of unprocessed data to knowledge: The user’s perspective Guido Jenster, Ph.D. Professor of Experimental Urological Oncology Department.
Centralizing Bioinformatics Services: Analysis Pipelines, Opportunities, and Challenges with Large- scale –Omics, and other BigData High-Performance Computing.
Xiaole Shirley Liu STAT115, STAT215, BIO298, BIST520
Pathway Informatics 16th August, 2017
Introduction to Bioinformatics and Functional Genomics
Optimizing Biological Data Integration
Bioinformatic Tools for Epigenetic Research
Ensembl Genome Repository.
ChIP-seq Robert J. Trumbly
Presentation transcript:

Bioinformatics for genomics Kickoff Bioinformatics Expertise Center 10 November 2009 Judith Boer Dept. of Human Genetics

Omics views of genomes RNA expression Gene structure Genetic variationExpression variation DNA methylation Chromatin Epigenetic variation SNPs, loss-of-heterozygosity Copy number variants

Who are we? Johan den Dunnen  always new machines Peter-Bram ‘t Hoen  always new applications Barend Mons  biosemantics Peter Taschner  databases and annotation Matt Hestand  next generation sequencing analysis Judith Boer  microarray and integrated analysis

Bioinformatics at Human Genetics Personal view: "Life science researchers should be able to analyze and interpret their own genomics data" Tools Courses Research - example Expertise

Bioinformatics Tools – Commercial Rosetta Resolver database, analysis, visualization Spotfire analysis and visualization Ingenuity Pathway Analysis literature and high-throughput database mining Dedicated platform tools Agilent, Illumina, Affymetrix: image analysis, per array

Bioinformatics Tools – Open source Programming languages R, Perl, Bash scripting (Linux), MySQL, Apache, PHP, Python, Java, … Software, e.g. Bioconductor, BioPerl, Ensembl Perl API, Bowtie, BWA, Velvet, Varscan, Rmap, … Alignment, analysis of next-generation sequencing and microarray data Web browsers, e.g. UCSC, Ensembl visualize data in relation to genome features Gene Ontology, e.g. DAVID functional annotation and enrichment

Bioinformatics Research & Tools BioSemantics Databases and annotation Next generation sequencing analysis Microarray and integrated analysis

Bioinformatics Tools – BioSemantics Anni 2.1 (Jelier / Mons / 't Hoen) associations between gene list and other genes, diseases, processes based on literature mining Nermal (van Haagen / Mons / 't Hoen) which proteins associate with / bind to my protein?

Bioinformatics Tools – NGS analysis GAPSS (Hestand / van Galen / 't Hoen) modular pipeline for next-generation sequencing data analysis CORE_TF (Hestand / 't Hoen) Conserved and Over-REpresented Transcription Factor binding sites

Bioinformatics Tools – Databases LOVD (Fokkema / Taschner) locus-specific DNA variation database Mutalyzer (Fokkema / Taschner) sequence variant nomenclature check

Bioinformatics Tools – Microarray analysis Microarray Retriever (Brandt / 't Hoen) search and retrieve data from public array repositories R packages (Menezes / van Iterson / Boer) SIM: Statistical Integration of Microarrays SSPA: Sample Size and Power Analysis for microarray data

Bioinformatics Courses Analysis of microarray gene expression data (MGC) Judith Boer, Peter van der Spek (ErasmusMC) 10th edition June 2010 (yearly, participants PhD/PD) Next-generation sequencing data analysis (MGC) Johan den Dunnen, Judith Boer, Matt Hestand 3rd edition planned February others: MolMed Research School ErasmusMC, NBIC

Bioinformatics Research – Example Next generation sequencing data analysis ChIP-seq gene structure (DeepCAGE) expression analysis (DeepSAGE) miRNA expression and identification (targeted) re-sequencing mutation (SNP) detection copy number variation detection de novo assembly

Bioinformatics Expertise Experimental design of microarray and NGS studies Choice of analysis software Use of analysis software Setting up a locus-specific database Some cases: help with data analysis

Acknowledgements BioSemantics: Herman van Haagen, Bharat Singh, Peter-Bram ‘t Hoen, Marco Roos, Barend Mons Databases and annotation: Ivo Fokkema, Jacopo Celli, Gerard Schaafsma, Jeroen Laros, Peter Taschner NGS analysis: Michiel van Galen, Jaap van der Heijden, Yuching Lai, Henk Buermans, Matthew Hestand Microarray analysis: Maarten van Iterson, Judith Boer Michel Villerius, Johan den Dunnen, Gertjan van Ommen