Download - Data analytics challenges in genomics
Data analysis challenges in genomics
Guest lecture, Data Mining
Uppsala 2013-10-08
Mikael Huss
Science for Life Laboratory / Stockholm University
Where I work
Science for Life Laboratory Stockholm, at Karolinska institutet science park
A national center for high throughput biology (ie massively parallel measurements of DNA/RNA (“genomics”, “next generation DNA sequencing”), proteins (“proteomics”, mass spectrometry) etc.
Nodes in Uppsala & Stockholm; funded by strategic grants
Offers services to customers, mostly DNA sequencing + associated analysis
Outline
1. Context (short intro to DNA sequencing)
2. Big goals / visions
3. Examples of data mining applications and technical challenges
1. Some context on DNA sequencing
All* living organisms have DNA as their blueprint
GTTACGTAACCGTTACGTA…..CCTTGATCGTAAC….Etc. (2x3 billion letters for humans)
*OK, some viruses have RNA
?
DNA Blueprint / source codePretty much identical in all your cells
RNA “Expressed”, “active” genesDiffers between tissues, cell types, disease vs health
Proteins The molecules that actually do stuff
…ACGT…
…ACGU…
…KVL…
Reading the nucleotide or amino acids is called sequencing
It is easier to isolate and therefore to sequence DNA and RNA
DNA sequencing means “reading the genome”RNA sequencing can be used to get a snapshot of the active genesProtein abundance can be measured but harder to do on a massive scale
A short refresher on molecular genetics!
(http://ds9a.nl/amazing-dna)
SciLifeLab
Presently sequencing ~3 megabases of DNA per second
Corresponding to about 3 human genome sizes per hour
Also RNA, protein measurements
What is sequencing good for?
- Mapping new genomes
- Comparing individual genomes to each other
- Looking at how genes are expressed (RNA sequencing)
De novo genome sequencing
Arabidopsis (0.12 Gbp)
Populus (0.45 Gbp)
Humans (3 Gbp)
Co
nife
rs(2
0 G
bp)
Spruce(20 Gbp)
Mapping new genomes
E. g. Norwegian spruce (Christmas tree)
Economically the most important Swedish tree
Provide basis for research on• tools for breeding for tree productivity, quality, health• tools for cellulose and wood fibre modification (new
materials)
Working in the context of a known reference genome.
Common application: Looking for genes responsible for hereditary diseases
Often rare monogenic or common complex diseases
More than 6,000 known monogenic disease
Only ~ ½ have a gene associated (OMIM)
Complex diseases – diabetes, asthma, MS, ….
Resequencing and variation analysis
Functional genomics
Variation between
-Tissues- Cell types- Cell states-Individuals
- How genes actually get expressed
Functional genomics
Furusawa and Kaneko, Biology Direct 2009 4:17
Transcriptional patterns
“cell types” as attractors in systems of interacting genes
2. Big goals / visions
Big goals / visions
• Precision medicine – Genomic medicine– Personalized medicine– Individualized treatments
• Understanding natural diversity– Discovering new organisms– Mapping ecological niches
• Understanding complex diseases– Molecular definitions of diseases– Lifestyle and epigenetics
Big goals / visions
• Precision medicine – Genomic medicine– Personalized medicine– Individualized treatments
• Understanding natural diversity– Discovering new organisms– Mapping ecological niches
• Understanding complex diseases– Molecular definitions of diseases– Lifestyle and epigenetics
Mount Sinai Medical Center / Eric Schadt
Personal sequencing?
Genomics apps
Community genomics & crowdsourced clinical trials
https://www.23andme.com/about/factoids/
Exploring the human microbiome
Estimated 10x more bacterial cells than human cells in human body
Three “enterotypes”
Personal microbiome sequencing
Big goals / visions
• Precision medicine – Genomic medicine– Personalized medicine– Individualized treatments
• Understanding natural diversity– Discovering new organisms– Mapping ecological niches
• Understanding complex diseases– Molecular definitions of diseases– Lifestyle and epigenetics
Environmental samples: soil, ocean etc
Identifying new viruses in human or environmental samples; <1% known so far
http://www.ted.com/talks/nathan_wolfe_what_s_left_to_explore.html
Planetary ecologyPerhaps: “genomic observatories” continuously monitoring environmental DNA
streaming, real-time analysis important
Big goals / visions
• Precision medicine – Genomic medicine– Personalized medicine– Individualized treatments
• Understanding natural diversity– Discovering new organisms– Mapping ecological niches
• Understanding complex diseases– Molecular definitions of diseases– Lifestyle and epigenetics
Complex diseases
• Cardiovascular disease• Autoimmune disease
– Rheumatism– Multiple sclerosis– Psoriasis– …
• Diabetes(etc.)
No simple genetic explanation.
Lifestyle & environment factors likely important.
Data integration and correlative analysis
http://techcrunch.com/2012/03/29/cloud-will-cure-cancer/
“Collecting comprehensive profiles of every tumor for every patient provides a dataset to build models that learn normal cellular function from cancerous deviations.
Diagnostics and treatment companies/hospitals/physicians can then use the models to deliver therapy.
If we imagine a world where every tumor is comprehensively profiled, it quickly becomes clear that not only will the data sets be very large but also involve different domains of expertise required for quality control, model building, and interpretation.”
Cancer – not one disease
Genes – Epigenetics – Lifestyle - Environment
Understanding the interplay of lifestyle (including environment) and genes through the “interface layer”, epigenetics.
Massive correlational analyses …
Epigenetics and lifestyle
epigenetics – changes in gene expression that are not due to base sequence changes (and that can be passed on to daughter cells during cell division)
Gigantic clinical sequencing projects
Genomics England / NHS will sequence 100,000 genomes of patients in the next 5 years
… BGI aims for a million
But are we ready to interpret genomes?
3. Applications and challenges of data mining in genomics
Storage and transfer
“European Bioinformatics Institute (EBI) stores 20 pb of data, of which 2 pb is genomic”
“Single human genome ~140 Gb”
“ … downloading the data is time-consuming, and researchers must be sure that their computational infrastructure and software tools are up to the task. “If I could, I would routinely look at all sequenced cancer genomes,” says [Arend] Sidow. “With the current infrastructure, that's impossible.”
Cloud solutions:Embassy Cloud – EBI + CSC in EspooeasyGenomics – BGI Hong KongDNANexus – commercial service, Silicon Valley
Analysis challenges
Dealing with the size of raw data
Growth in sequencing capacity has outstrippedMoore’s law
Need to throw away data Tailored streaming / approximate algorithms
The Economist
Shape of data
“Commercial” big data:
(e.g. purchase data, movie ratings, “likes”, cell phone locations, tweets)- Typically cheap to collect examples (data points) -> many observations- Usually low-dimensional (few features)- Data are informative only in aggregate (each data point is almost meaningless)
Biomedical big data:
(e.g. DNA sequencing, fMRI etc)- Typically expensive to collect data points -> few observations- Usually very high dimensional (e.g. ~20.000 gene measurements)- Underpowered for modelling, much more features than observations
So, biological data often seems to be “transposed” relative to other types(“large p, small n”)
10-250 million such entries for one sample in an experiment
20.000-row x 125-column matrix Perhaps 3 million rows
Gene expression Genetic variants
The shape of (raw and processed) data
Examples of data mining applications in genomics
• Classification– Diseases and disease subtypes– Biomarkers for disease– Predicting disease presence or
subtype from gene expression• Clustering and visualization
– Defining cell types– Molecular definitions of disease
• Association rules– Text analysis
Electronic health records
Mining electronic health records: towards better research applications and clinical care
Peter B. Jensen, Lars J. Jensen & Søren Brunak
Nature Reviews Genetics 13, 395-405 (June 2012)
Unstructured and structured textMedication historyTest resultsDemographics(etc)
Genome interpretation
Sugino et al, Molecular taxonomy of major neuronal classes in theadult mouse forebrain, Nature Neuroscience 9, 99 - 107 (2005)
Gene expression patterns and neuronal cell types
Cell types
Gen
es
Gene expression
Shape and behavior of neurons
Genetics of multiple sclerosis
• Gene expression data on ~120 patients and 70 controls• Medication, lifestyle, specific diagnosis• Environment important – sunlight, tobacco etc
Gene expression
Medication, diagnosis etc
Predictive analysis contests
Predictive analysis contests
Science-oriented
• Build predictive models for classifying gene expression signatures for:– Psoriasis– Multiple sclerosis– COPD– Lung cancer
• Training set is public data, the secret test set was proprietary
SBV Improver Challenge #1
• Build predictive models for classifying gene expression signatures for:– Psoriasis– Multiple sclerosis– COPD– Lung cancer
• Training set is public data, the secret test set was proprietary
SBV Improver Challenge #1
SBV Improver Challenge #1
• Psoriasis easy• Lung cancer hard• MS diagnostic, COPD somewhere in the middle• MS subtype: no statistically significant submissions!
https://www.sbvimprover.com/sbv-improver-symposium-2012-presentations
Species translation challenge
- Can the perturbations of signaling pathways in one species predict the response to a given stimulus in another species?
- Which computational methods are most effective for inferring gene, phosphorylation and pathway responses from one species to another?
CAMDA 2013 challenges
Question 1: Can we replace the animal study with an in vitro assay? The current safety assessment is largely relied on the animal model, which is time-consuming, labor-intensive, and definitely not in line with the animal right voice. There is a paradigm shift in toxicology to explore the possibility of replacing the animal model with in vitro assay coupled with toxicogenomics. The TGP data contains both in vitro and animal data, which is essential to address this question.
Question 2: Can we predict the liver injury in humans using toxicogenomics data from animals?
Available data:
Drug Information (Excel table) – the basic information about individual drugs from DrugBank
Pathology Data (Excel table) –Pathology and clinical chemistry data for each rat
Array Metadata (csv format) – Meta data (e.g., dose, time, sacrifice time and etc)“toxicogenomics”
Fully open code that runs on the server to generate predictions. Can build on others’ results