Recommended
Recommended
More Related Content
What's hot
What's hot (20)
Viewers also liked
Viewers also liked (20)
Similar to Computational challenges in precision medicine and genomics
Similar to Computational challenges in precision medicine and genomics (20)
Recently uploaded
Recently uploaded (20)
Computational challenges in precision medicine and genomics
- 1. COMPUTATIONAL CHALLENGES IN PRECISION MEDICINE AND GENOMICS GARY BADER WWW.BADERLAB.ORG GOOGLE WATERLOO, JUNE 9, 2014
- 2. PRECISION MEDICINE • TRADITIONAL MEDICINE, WITH MORE DATA • DIAGNOSIS: ASSIGNING PATIENTS TO GROUPS – BIOLOGY, DISEASE PROGRESSION, TREATMENT RESPONSE • PERSONALIZED, BUT NOT EVERYONE HAS A DIFFERENT DISEASE NATURE MEDICINE 19, 249 (2013) DOI:10.1038/NM0313-249
- 3. NATIONAL COMPREHENSIVE CANCER NETWORK (NCCN) Breast Cancer Noninvasive Invasive Lobular Carcinoma In Situ Ductal Carcinoma In Situ Lobular Carcinoma Ductal Carcinoma Inflammatory
- 4. IMPROVING PRECISION WITH GENOMICS • BRCA1/BRCA2 MUTATIONS PREDICT RISK • COMMERCIAL PROGNOSTIC TESTS BASED ON GENE SIGNATURES HTTP://THEBIGCANDME.BLOGSPOT.CA/
- 5. GENOMICS • NEW TECHNOLOGY FOR READING/WRITING DNA • MEASURE OUR GENETIC CODE AND SYSTEM STATE • LOTS OF VARIABLES – WHOLE GENOME, TRANSCRIPT AND PROTEIN EXPRESSION, SPLICING, CHROMATIN STRUCTURE, MOLECULAR INTERACTION, TRANSCRIPTION FACTOR, METHYLATION, METABOLITE, PATIENT PHENOTYPE
- 6. 2
- 7. HTTP://WWW.LHSC.ON.CA/ SOURCE CODE ON DISK LOAD TO ACTIVE MEMORY COMPILER RUNNING SOFTWARE ACTIVE MEMORY 4 LETTER CODE (DNA/RNA BASES) 20 LETTER CODE (AMINO ACIDS) MEEPQSDPSVEPPLSQETFSDLWKLLPEN…GATGGGATTGGGGTTTTCCCCTCCCAT…
- 8. A PROTEIN IS A MOLECULAR MACHINE
- 9. DNA SEQUENCING • RECENT MASSIVE BREAKTHROUGH • CURRENT TECH: – ~10 HUMAN GENOMES, 1TB DATA/6 DAY RUN ILLUMINA, GEORGE CHURCH
- 10. FEB. 1, 2013: DR. LEE HOOD RECEIVES HIS NATIONAL MEDAL OF SCIENCE FROM PRESIDENT OBAMA AT WHITE HOUSE CEREMONY
- 11. MORE BREAKTHROUGHS COMING WWW.NANOPORETECH.COM 20-NODE INSTALLATION = COMPLETE HUMAN GENOME IN 15 MINUTES MINION = USB CONNECTION, MINIMAL SAMPLE PREPARATION, $1000 DEVICE + CONSUMABLES
- 12. WHERE DOES THE DATA COME FROM? BARODA, INDIA TORONTO, CANADA VERMONT, USA CAMBRIDGE, UK MOLECULAR BIOLOGY LABS AROUND THE WORLD
- 13. BGI, >160 MACHINES THE FACTORY
- 14. COMPUTING NEEDS: 1 HUMAN GENOME • ~125 BASE READ LENGTH X MILLIONS • >30X COVERAGE • ALIGNMENT TO REFERENCE GENOME • COMPUTE VARIANTS (MUTATIONS) • ANNOTATE VARIANTS • COMPUTE TIME: UP TO 2 DAYS/GENOME – OPTIMIZED 4 HOURS: 128G/2CPU/SSD, 3.1GHZ • MEDICALLY IMPORTANT TO BE FAST
- 15. THE POWER OF GENOMICS IN MEDICINE • 7000 RARE MONOGENIC DISEASES – 50% HAVE A KNOWN GENE RESPONSIBLE – QUADRUPLED RATE OF IDENTIFICATION SINCE 2012 • BRAIN DOPAMINE-SEROTONIN VESICULAR TRANSPORT DISEASE AND ITS TREATMENT – TWO YEARS FROM DISEASE DEFINITION TO GENE IDENTIFICATION TO TREATMENT NAT REV GENET. 2013 OCT;14(10):681-91 N ENGL J MED. 2013 FEB 7;368(6):543-50
- 18. CANCER GENOMICS • GERM LINE VS. SOMATIC MUTATIONS • AIM: IDENTIFY FREQUENT MUTATIONS IN CANCER • >11,000 TUMOUR GENOMES, 9M MUTATIONS HUMAN COLORECTAL CARCINOMA HTTPS://DCC.ICGC.ORG/
- 19. COMPUTING CHALLENGES • EXPONENTIAL DATA GROWTH (>MOORE’S LAW) – BILLIONS OF GENOMES – SIZE: >100GB/HUMAN GENOME, 4GB PROCESSED, MBS (JUST MUTATIONS) • HETEROGENEOUS, NOISY, COMPLEX DATA – DATA SCIENTISTS, DOMAIN EXPERTS
- 20. COMPUTING WILL TRANSFORM MEDICINE GOAL: IMPROVE PATIENT OUTCOME
- 21. COMPUTATIONAL BIOLOGY • RESEARCH: USING COMPUTERS TO ANSWER BIOLOGICAL/BIOMEDICAL QUESTIONS • EXPLORE, INTERPRET AND DISCOVER: SEARCH • SPEED AND ACCURACY: ALGORITHMS • PREDICTING FUNCTIONAL MUTATIONS, PATIENT CLASSIFICATION: MACHINE LEARNING • PRIVACY: DIFFERENTIAL PRIVACY, ENCRYPTION • USABLE APPLICATIONS: SOFTWARE ENGINEERING
- 22. MedSavant search engine for genetic variants WWW.MEDSAVANT.COM Developers: Marc Fiume, James Vlasblom, Ron Ammar, Orion Buske, Eric Smith, Andrew Brook, Misko Dzamba, Khushi Chachcha, Sergiu Dumitriu Scientific Advisors: Christian Marshall, Kym Boycott, Marta Girdea, Peter Ray, Gary Bader, Michael Brudno
- 26. GLIOBLASTOMA MULTIFORME (N=215) GOLDENBERG, BRUDNO NATURE METHODS, 2014IDENTIFY DISEASE SUBTYPE SURVIVAL CLUSTERING SPEED DATA FUSION (NON-LINEAR, MESSAGE PASSING), UNSUPERVISED CLUSTERING
- 27. PREDICT TREATMENT RESPONSE • SUPERVISED MACHINE LEARNING E.G. RHEUMATOID ARTHRITIS METHOTREXATE RESPONSE B New A A B B B A Personal Medical Network Responder Non-Responder New New patient (Predicted Non-Responder) Weakly similar Highly similar Response to treatment A Similar e.g. SNP, smoking status SHIRLEY HUI, RUTH ISSERLIN, HUSSAM KACA, TABITHA KUNG, KATHY SIMINOVITCH
- 28. EXPLAINING GENOMICS DATA • SNAPSHOTS OF SYSTEM STATE – E.G. CANCER VS. NORMAL • EXPLAIN WHY STATES DIFFER – E.G. REGULATOR PERTURBATION – CAUSAL MODELING – PRIOR KNOWLEDGE ABOUT MECHANISM: PATHWAYS WITT H ET AL. CANCER CELL. 2011 AUG 16;20(2):143-57
- 29. GENOME++ MOLECULAR, PHYSIOLOGICAL PHENOTYPE ENCODES EXPLAINS ENVIRONMENT CELL MECHANISM THE HUMAN BODY • A WETWARE COMPUTING SYSTEM MODULATES
- 30. A PROTEIN IS A MOLECULAR MACHINE
- 33. HO ET AL. NATURE 415(6868) 2002
- 35. THE CELL
- 36. ALAIN VIEL, HARVARD UNIVERSITY, 2007
- 37. HTTP://WWW.ENDOSZKOP.COM/ ~40 TRILLION CELLS, +TRILLIONS OF MICROBES (PARALLEL PROCESSING) BIANCONI ET AL. ANN HUM BIOL. 2013 NOV-DEC;40(6):471
- 38. Microtubule Cytoskeleton Cell Projection & Cell Motility Cell Proliferation Glycosylation Adhesion Regulation of GTPase Kinase Activity/Regulation CNS Development Intellectual Disability Autism GTPase/Ras Signaling Regulation of cell proliferation Positive regulation of cell proliferation Tyrosin kinase Vasculature develepment Palate develepment Organ Morphogenesis Behavior Heart develepment RHO Ras Membrane Kinase regulation Cell Motility (stricter cluster) Centrosome Nucleolus Cell cycle Regulation of hormone levels Aminoacid derivative / amine metabolism Synaptic vescicle maturation Reelin pathway LIS1 in neuronal migration and development Negative regulation of cell cycle cKIT pathwaymTor pathway Zn finger domain Carboxyl esterase domain Ras signaling GTPase regulator Neuron migration Cell Motility (stricter cluster) Cell morphogenesis Cell projection organization CNS development Brain development Neurite development CNS neuron differentiation Axonogenesis Projection neuron axonogenesis Cerebral cortex cell migration SMC flexible hinge domain Urea and amine group metabolism MHC-I Zoom of CNS-Development ID ID ASDASD Both 0% 12.5% Enriched in deletions FDR Known disease genes Enriched only in disease genes Node type (gene-set) Edge type (gene-set overlap) From disease genes to enriched gene-sets Between gene-sets enriched in deletions Between sets enriched in deletions and in disease genes or between disease sets only Pinto et al. FuncJonal impact of global rare copy number variaJon in auJsm spectrum disorders. Nature. 2010 Jun 9.
- 39. Adhe Reelin pathway development Nega regula of cell Neuron migration Cell Motility (stricter cluster) Cell morphogenesis Cell projection organization CNS development Brain development Neurite development CNS neuron differentiation Axonogenesis Projection neuron axonogenesis Cerebral cortex cell migration Zoom of CNS-Development
- 40. PATIENT #1 PATIENT #2 PATIENT #3 PATIENT #I PATHWAYGSI CNV-AFFECTED GENE COUNT = 1 COUNT = 1 COUNT = 1 COUNT = 0 • IF WE HAVE AT LEAST ONE CNV AFFECTING AT LEAST ONE GENE IN A CERTAIN PATHWAY GI, THEN WE HAVE A PERTURBATION POTENTIAL IN THAT PATHWAY • WE COUNT THE PRESENCE / ABSENCE OF SUCH PERTURBATION POTENTIAL IN PATIENTS PaJent #1 PaJent #2 PaJent #3 … PaJent #i … PaJent #n GS1 1 1 1 … 0 … 0 GS2 0 0 1 … 1 … 0 GS3 0 0 0 … 0 … 0 DANIELE MERICO PATHWAY ASSOCIATION TEST
- 41. DESCRIPTION: • THE SIGNIFICANCE OF A GENE-SET IS THEN ASSESSED USING THE FISHER S EXACT TEST FOR ASSOCIATION • A SIGNIFICANT GENE-SET IS AFFECTED BY A MUTATION POTENTIAL MORE FREQUENTLY IN CASES THAN CONTROLS • THE FDR IS ESTIMATED BY SHUFFLING THE COLUMNS IN THE GENE-SET BY PATIENT COUNT TABLE Case Control GSi 13 1 Not in GSi 1146 -‐ 13 889 -‐ 1 PaJent #1 PaJent #2 PaJent #3 … PaJent #i … PaJent #n GS1 1 1 1 … 0 … 0 GS2 0 0 1 … 1 … 0 GS3 0 0 0 … 0 … 0 PATHWAY ASSOCIATION TEST
- 43. BENEFITS OF SYSTEMS THINKING • IMPROVES STATISTICAL POWER – FEWER TESTS • MORE REPRODUCIBLE – E.G. GENE EXPRESSION SIGNATURES • EASIER TO INTERPRET – FAMILIAR CONCEPTS E.G. CELL CYCLE • IDENTIFIES MECHANISM – CAN EXPLAIN CAUSE VS. PARTS THINKING
- 44. DATABASESEXPERIMENTS, PREDICTIONS LITERATURE EXPERTS GENOME++ MOLECULAR, PHYSIOLOGICAL PHENOTYPE ENCODES EXPLAINS ENVIRONMENT CELL MECHANISM MODULATES
- 46. THE FACTOID PROJECT MAX FRANZ, IGOR RODCHENKOV, OZGUN BABUR, EMEK DEMIR, CHRIS SANDER HELPING AUTHORS DIGITIZE THEIR PUBLISHED KNOWLEDGE HTTP://FACTOID.BADERLAB.ORG/
- 47. NETWORK VISUALIZATION AND ANALYSIS UCSD, ISB, AGILENT, MSKCC, PASTEUR, UCSF HTTP://CYTOSCAPE.ORG PATHWAY COMPARISON LITERATURE MINING GENE ONTOLOGY ANALYSIS ACTIVE MODULES COMPLEX DETECTION NETWORK MOTIF SEARCH
- 48. CYTOSCAPE.JS: HTML5 – TOUCH CYTOSCAPE.GITHUB.COM/CYTOSCAPE.JS/ MAX FRANZ
- 49. GENE FUNCTION PREDICTION HTTP://WWW.GENEMANIA.ORG QUAID MORRIS (DONNELLY) RASHAD BADRAWI, OVI COMES, SYLVA DONALDSON, MAX FRANZ, CHRISTIAN LOPES, FARZANA KAZI, JASON MONTOJO, HAROLD RODRIGUEZ, KHALID ZUBERI • GUILT-BY-ASSOCIATION PRINCIPLE • BIOLOGICAL NETWORKS ARE COMBINED INTELLIGENTLY TO OPTIMIZE PREDICTION ACCURACY • ALGORITHM IS MORE FAST AND ACCURATE THAN ITS PEERS
- 50. SOCIAL CHALLENGES • BIOETHICS AND DATA SHARING • ENGAGING RESEARCHERS – CROWDSOURCING: TCGA PAN CANCER, DREAM • ENCOURAGING RESEARCHERS TO EXPLORE UNCHARTED TERRITORY • NEED FOR QUANTITATIVE THINKING IN BIOLOGY – NEW PH.D. PROGRAM IN THE MOLECULAR GENETICS DEPARTMENT AT THE UNIVERSITY OF TORONTO NATURE. 2011 FEB 10;470(7333):163-5WWW.NATURE.COM/TCGA/
- 51. EPENDYMOMA • 3RD MOST COMMON BRAIN TUMOUR IN CHILDREN • INCURABLE IN UP TO 45% OF PATIENTS STEVE MACK, MICHAEL TAYLOR, RUTH ISSERLIN -‐ CANCER CELL. 2011 AUG 16;20(2):143-‐57 GENE EXPRESSION PATIENT AGE OVERALL SURVIVAL
- 52. EPENDYMOMA GENOMIC ANALYSIS • EPENDYMOMA BRAIN CANCER -‐ MOST COMMON AND MORBID LOCATION FOR CHILDHOOD IS THE POSTERIOR FOSSA (PF = BRAINSTEM + CEREBELLUM) • TWO SUBTYPES BY GENE EXPRESSION: PFA -‐ YOUNG, DISMAL PROGNOSIS, PFB -‐ OLDER, EXCELLENT PROGNOSIS. • WHOLE GENOME SEQUENCING (47 SAMPLES) SHOWED ALMOST NO MUTATIONS, HOWEVER DNA METHYLATION ARRAYS SHOWED CLEAR CLUSTERING INTO PFA AND PFB (79 SAMPLES) • PFA MORE TRANSCRIPTIONALLY SILENCED BY CPG METHYLATION STEVE MACK, MICHAEL TAYLOR, SCOTT ZUYDERDUYN NATURE, FEB. 2014
- 53. POLYCOMB REPRESSOR COMPLEX 2 – INHIBITED BY DZNEP AND GSK343 – KILLED PFA CELLS NO KNOWN TREATMENT, SO NOW GOING TO CLINICAL TRIAL, COMPASSIONATE USE IN ONE PATIENT
- 54. 2 MONTHS 3 MONTHS 3 CYCLES VIDAZA 9 YO WITH METASTATIC PF EPENDYMOMA TO LUNG TREATED WITH AZACYTIDINE TREATMENT OF METASTATIC PF EPENDYMOMA WITH VIDAZA MICHAEL TAYLOR
- 55. ACKNOWLEDGEMENTS BADER LAB DOMAIN INTERACTION TEAM SHOBHIT JAIN BRIAN LAW JÜRI REIMAND MOHAMED HELMY ANDREA UETRECHT MARINA OLHOVSKY CANCER GENOMICS FLORENCE CAVALLI DAVID SHIH ASHA ROSTAMIANFAR PRECISION MEDICINE RON AMMAR SHIRLEY HUI FUNDING HTTP://BADERLAB.ORG PATHWAY AND NETWORK ANALYSIS RUTH ISSERLIN IGOR RODCHENKOV SCOTT ZUYDERDUYN RUTH WONG VERONIQUE VOISIN SHAHEENA BASHIR KHALID ZHUBERI CHRISTIAN LOPES JASON MONTOJO MAX FRANZ HAROLD RODRIGUEZ