Madrid icgc pcawg_2016_slideshare

Canceromatic III - Session I: Pan-Cancer analysis - Changing landscape of data and tools available for reproducible cancer genomics workflows: report from the ICGC trenches.

Nov 14th 2016B.F. Francis Ouellette francis@oicr.on.ca

• Senior Scientists & Associate Director, Informatics and Biocomputing, Ontario Institute for Cancer Research, Toronto, ON

• Associate Professor, Department of Cell and Systems Biology, University of Toronto, Toronto, ON.

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Module 2 bioinformatics.ca

ONTARIO INSTITUTE FOR CANCER RESEARCH

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francis@oicr.on.caE-mail

Cancer-om-atics Jul 6-9 2009Cancer-om-atics II Mar 28-30 2011Canceromatics III Nov 13 -16 2016

DisclaimersI do not (and will not) profit in any way, shape or form, from any of the brands, products or companies I may mention.

I am a big proponent of Open Access, Open Source, Opent Data and Open Courseware

I am on the SAB of many NIH funded projects (SGD, Galaxy, GenomeSpace, H3ABionet, and HMP2), as well as Elixir and Genome Canada’s SIAC, and the NRC’s KMAC. This comes with a bias on how science should be done!

Outline

IntroductionICGCPCAWGClosing remarks

adapted from https://goo.gl/fQJAz1

ICGC PCAWGDocker Testing

Cancer is a Disease of the Genome

Challenge in Treating Cancer: Every tumour is different Every cancer patient is different

Adapted from Tom Hudsonhttps://www.cancer.gov/research/areas/genomics

Johns Hopkins> 18,000 genes analyzed for mutations11 breast and 11 colon tumorsL.D. Wood et al, Science, Oct. 2007

Wellcome Trust Sanger Institute518 genes analyzed for mutations210 tumors of various typesC. Greenman et al, Nature, Mar. 2007

TCGA (NIH)Multiple technologiesbrain (glioblastoma multiforme), lung (squamous

carcinoma), and ovarian (serous cystadenocarcinoma).

F.S. Collins & A.D. Barker, Sci. Am, Mar. 2007

Large-Scale Studies of Cancer Genomes

Heterogeneity within and across tumor types

High rate of abnormalities (driver vs passenger)

Sample quality matters Consent and controlled data access is

complicated

Lessons learned from early studies

MR Stratton et al. Nature 458, 719-724 (2009) doi:10.1038/nature07943

Analysis Data TypesSimple Somatic Mutations (SSM or SNV)Copy Number Alterations (CAN or CNV)Structural Variants (SV) Germline variants (SNPs)Gene Expression (micro-arrays and RNASeq)miRNA Expression (RNASeq)Epigenomics (Arrays and Methylation) Splicing Variation (RNASeq)Protein Expression (Arrays)

Rationale for the ICGC:

Scope is hugeReduce duplication of effortStandardization and uniform quality measuresMerging of datasetsSpectrum of many cancers varies across the worldAccelerate the dissemination of genomic and analytical methods

International Cancer Genome Consortium

Collect ~500 tumour/normal pairs from each of 50 different major cancer types; 25,000 T/N pairs!

Comprehensive genome analysis of each T/N pair: GenomeTranscriptomeMethylomeClinical data

Make the data available to the research community & public. Identify

genome changes

…GATTATTCCAGGTAT… …GATTATTGCAGGTAT… …GATTATTGCAGGTAT…

Adapted from Tom Hudson

International Cancer Genome Consortium: http:/icgc.org

DataSubmissio

ValidationValidationValidation(dictionary)

Validation(across fields)Validation

(across fields)Validation

(across fields)

indexing

Happy Users

http://goo.gl/1EcyR

ICGC needs to deal with different kinds of users!

Biologists/Clinicians:Web interface to processed data, providing:

Affected gene lists with consequencesImpact on pathways

Power users:Application Programing Interface (API) to get to dataAvailability and Integration with cloud resources

ICGC Data Coordinating Centre: dcc.icgc.org

BRAF missense mutations in colorectal cancer

https://dcc.icgc.org/

https://dcc.icgc.org/icgc-in-the-cloud

http://www.cancercollaboratory.org/

http://docs.icgc.org/

User and submitter documentation

Software development discussions

https://discuss.icgc.org/

Some challenges:

So, we have lots of data, is it generated the same way?

Every country/group has basically been submitting:

Simple Somatic Mutations (SSM or SNV)Copy Number Alterations (CAN or CNV)Structural Variants (SV) Germline variants (SNPs)Gene Expression (micro-arrays and RNASeq)miRNA Expression (RNASeq)Epigenomics (Arrays and Methylation) Splicing Variation (RNASeq)Protein Expression (Arrays)

Are they all using the same pipelines?

http://goo.gl/CekF6y

Missing Clinical Data?

http://goo.gl/CekF6y

Are we all using the same definition for controlled access data?

ICGCBAM/FASTQ

TCGABAM/FASTQ

ICGCOpenData

(includes TCGA

Open Data)

• Detailed Phenotype and Outcome data Region of residenceRisk factorsExaminationSurgeryRadiationSampleSlideSpecific histological featuresAnalyteAliquotDonor notes

• Gene Expression (probe-level data)• Raw genotype calls• Gene-sample identifier links• Genome sequence files

ICGC Controlled Access Datasets

• Cancer Pathology Histologic type or subtypeHistologic nuclear grade

• Patient/Person Gender, Age range, Vital status, Survival timeRelapse type, Status at follow-up

• Gene Expression (normalized)• DNA methylation •Computed Copy Number and Loss of Heterozygosity• Newly discovered somatic variants

ICGC OA Datasets

http://goo.gl/w4mrV

Differences between ICGC & TCGA• Different tumour types• Different geographic rules• Many countries vs one jurisdiction• Different definitions of what is controlled• Different data access rules

• Detailed Phenotype and Outcome data

• Gene Expression (probe-level data)

• Raw genotype calls

• Gene-sample identifier links

• Genome sequence files

• Germ line variants

ICGC Controlled Access Datasets

• Cancer Pathology Histologic type or subtypeHistologic nuclear grade

• Patient/Person Gender, Age range, Vital status, Survival timeRelapse type, Status at follow-up

• Gene Expression (normalized)• DNA methylation •Computed Copy Number and Loss of Heterozygosity• Somatic variants from Exome or WGS

ICGC OpenAccess Datasets

http://goo.gl/w4mrV

• Primary sequence data (BAM and FASTQ files)

• SNP6 array level 1 and level 2 data• Exon array level 1 and level 2 data• Somatic variants from whole

genome sequencing• Certain information in MAFs• A full list of controlled-access

data types can be found at: http://goo.gl/K1h7zu

TCGA Controlled Access Datasets

• De-identified clinical and demographic data

• Gene expression data• Copy number alterations in regions

of the genome• Epigenetic data• Summaries of data compiled across

individuals• Anonymized single amplicon DNA

sequence data• Somatic variants from scrubbed

exome sequencing

TCGA OpenAccess Datasets

http://goo.gl/A1rMRB

Can we do better?

From ICGC/TCGA

Each groups have been free to decide on their own if they wanted to sequence Exomes or Whole Genomes.A bit more than 10% of all genomes done were done with Whole Genome SequencingA steering comitte was formed and we decided to alnalyze these WG in a robust way with the primary question of figuring out what was hidden in the genomic sequence of cancer patients!

Steering Committee of PCAWG

Peter Campbell, Sanger Inst.Gady Getz, BroadJan Korbel, EMBLLincoln Stein, OICRJosh Stuart, UCSC

PanCancer Analysis of Whole Genomes (PCAWG)

> 2,800 T/N pairs with clinical data from 20 tumour type of whole genome analysis.Aligned with one standard pipeline.Genomic Variants determined with 3 pipelines17 working groupsStart writing papers now

Deliverable for PCAWG will include:

1st PANCANCER analysis on > 2,800 cancer tumours from a WGS perspectiveRNA, SSM, CNV, Methylation analysis & germlinePublished (executable) pipelines

Docker / DockstoreMutiple cloud access to dataMultiple portal access to data

https://dcc.icgc.org/pcawg

Working Groups (1/2)1 Novel somatic mutation calling methods 2 Analysis of mutations in regulatory regions3 Integration of transcriptome and genome4 Integration of epigenome and genome5 Consequences of somatic mutations on pathway and network activity6 Patterns of structural variations, signatures, genomic correlations, retrotransposons, mobile elements7 Mutation signatures and processes8 Germline cancer genome

Working Groups (1/2)9 Inferring driver mutations and identifying cancer genes and pathways10 Translating cancer genomes to the clinic11 Evolution and heterogeneity12 Exploratory: portals, visualization and software infrastructure13 Molecular subtypes and classification14 Analysis of mutations in non-coding RNA15 Exploratory: mitochondrial16 Exploratory: pathogensTech Technical working group

http://dockstore.org

PCAWG pipelines now on Dockstore

DOCKSTORE testing groupAndrew Duncan, OICRChristina Yung, OICRDenis Yuen, OICRZhibin Lu, OICRBrian O’Connor, UCSCAlex Buchanan, OHSUKyle Ellrott, OHSU Francis Ouellette, OICRGordon Saksena, BroadJunjun Zhang, OICRMiguel Vazquez, CNIOOliver Hofmann, AustraliaSolomon Shorser, OICRAdam Strucka, OHSU

Challenges:Too many conference calls!Too many clouds Even though we learned from what not to do with ICGC, we had to learn what not to do in the clouds.TCGA and ICGC have different authorization protocolsNot all data can exist everywhereDockstore testing is taking too long!

Other projects in planning ICGC to finish in Spring of 2018Planning for ICGCmed

ICGC 1: 25,000 tumours (DNA, RNA, Epigenome, Clinical data)ICGCmed: 200,000 Tumours (DNA, RNA, Epigenome, Clinical trial)ICGC1 was the picture, ICGCmed will be the movie (before and after treatment).

Submission system with one place for data and metadataTools/links directory portal

29,647

ONTARIO INSTITUTE FOR CANCER RESEARCHhttp://bioinformatics.ca/

0-Toronto1-Bethesda2-Hinxton

4-Queensland 3-Madrid5-Kyoto

7-Hidelberg 6-Cannes8-Toronto

9-Beijing

10-Mumbai11- Boston

Informatics & BioComputing @ OICR

Bioinformatics.ca workshops Content

http://bioinformatics-ca.github.io/

https://goo.gl/CGu13q1

DCC Software Developer

Vincent FerrettiDusan AndricPhuong-My DoFrancois GerthoffertTerry LinMichael MoncadaVitalii SlobodianykBob TiernayDouglas WongLinda XiangJunjun Zhang

AcknowledgmentsICGC/OICR Project leaders:

Tom HudsonJohn McPhersonLincoln SteinJared SimpsonPaul BoutrosVincent FerrettiFrancis OuelletteJennifer JenningsChristine Yung

Ouellette LabAlysha MoncrieffeAnn MeyerZhibin LuWeb DevJoseph YamadaKaman WuKim CullionKoji MiyauchiMiyuki Fukuma

ICGC DCC BiocurationHardeep NahalMarc Perry

http://oicr.on.ca http://icgc.org

… and all the patients and their families that that are putting their hopes into our work!

Research IT/Systems

David Sutton, Bob GibsonDavid MagdaRob NaccaratoBrian OttGino Yearwood

EGAJordi Rambla De ArgilaArcadi Navarro Audald Iloret Mauricio Moldes

http://icgc.orghttp://dcc.icgc.orghttp://docs.icgc.org

info@icgc.org http://bioinformatics.ca

We are hiring:

• OICR Director• Genome Technology Director• Junior Faculty in Informatics

& Biocomputing• PDFs

Interested? Ask Paul Boutros or I

Muchas gracias!

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