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Integration and analysis of multi-type high-throughput data for biomolecular knowledge discovery Dr. Erik Bongcam-Rudloff SGBC-SLU Uppsala, Sweden.

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Presentation on theme: "Integration and analysis of multi-type high-throughput data for biomolecular knowledge discovery Dr. Erik Bongcam-Rudloff SGBC-SLU Uppsala, Sweden."— Presentation transcript:

1 Integration and analysis of multi-type high-throughput data for biomolecular knowledge discovery Dr. Erik Bongcam-Rudloff SGBC-SLU Uppsala, Sweden

2 Biologists modus operandi Observing a phenomenon that is in some way interesting or puzzling. Making a guess as to the explanation of the phenomenon. Making a guess as to the explanation of the phenomenon. Devising a test to show how likely this explanation is to be true or false. Devising a test to show how likely this explanation is to be true or false. Carrying out the test, and, on the basis of the results, deciding whether the explanation is a good one or not. In the latter case, a new explanation will (with luck) 'spring to mind' as a result of the first test. Carrying out the test, and, on the basis of the results, deciding whether the explanation is a good one or not. In the latter case, a new explanation will (with luck) 'spring to mind' as a result of the first test. http : //www.biology.ed.ac.uk/archive/jdeacon/statistics/tress2.html http : //www.biology.ed.ac.uk/archive/jdeacon/statistics/tress2.html

3 The Observed phenomenon

4 Selection of test times

5 But was is the real event?

6 Sometimes you could be lucky Positive “Positive” results are used “negative” rejected Why? Only positive results are publishable “Positive” results are used “negative” rejected Why? Only positive results are publishable

7 Next Generation techniques

8 New challenges 1 TB data

9 Gbases produced at Sanger

10 World NGS Map http://omicsmaps.com/

11 But this is wonderful! Or? Sequence without knowledge connected to it is worth: 0 The deluge of data produced by these hordes of machines worldwide demand automatic workflows Complete new systems to shuffle data around Storage of never used amounts Machines with gigantic amounts of RAM

12 COSTS

13 PROBLEMS NOmenclature Publishing culture Moving target development Old ways of work and resistance to changes in culture

14 Publishing culture as example We get tax payers money, we pay publishers to publish, the publishers sell the articles and obtain the copy rights To connect knowledge to sequences we need automatic methods, workflows, text mining. Most of this is limited by close database systems. Only available is PubMed. But PubMed has only short abstracts. NO information about conditions, M&M etc We need to change this culture

15 The BLAST analogy... By far the most used tool by biologists Not possible if databases were not Open Access and freely searchable Imagine if Nucleotide and Protein databases followed the life science publishing model

16 BLAST

17 BLAST

18 BLAST

19 BLAST

20 BLAST

21 Human centric What about all other areas of the Life Sciences? Most genes are named by sequence similarity, but are the functions the same?

22 Microbiome http://www.secondgenome.com A microbiome is the totality of microbes, their genetic elements (genomes), and environmental interactions in a particular environment. microbesent.microbesent.

23

24 Fat and lean Metabolic effects of transplanting gut microbiota from lean donors to subjects with metabolic syndrome. A. Vrieze et al, EASD abstracts, 24 September 2012. The result was: Lean donor faecal infusion improves hepatic and peripheral insulin resistance as well as fasting lipid levels in obese individuals with the metabolic syndrome

25 Genome sizes

26 How many species? Several orders of magnitude: Some estimates: 3-50 million species of arthropods 1-100 million species of nematodes Only a portion of bacterias have being identified, 99% of bacterias cannot be cultured. “Once the diversity of the microbial worldis catalogued, it will make astronomy to look like a pitiful science” Julian Davies, Professor Emeritus. UBC

27 New research strategies MicrobialLivestockPlants

28 Typical Sources of Metagenomics Soil samples Sea water samples Air samples Medical samples Farm animal samples Ancient bones Human microbiome

29 Ion Proton: "Personal Genome Machine". LIFE TECHNOLOGIES CORPORATION Real tests of transcriptome sequencing on the Proton. Using 500 ng of input poly-A RNA, it was possible to generate 50 million reads from a melanoma cancer sample. Joe Boland of the National Cancer Institute according to Genomeweb.

30 Oxford Nanopore http://www.nanoporetech.com/

31 High technology everywhere!

32 New applications Only imagination will put the limits of what its possible to be done using Next Generation Technologies!

33 The big challenge: Open Access, Open source, collaborative networks Data sharing Common language Tool systems to glue all together!!

34 SeqAhead COST Action BM1006: Next Generation Sequencing Data Analysis Network. 2011-2014 COST Action 25 countries http://www.seqahead.euhttp://www.seqahead.eu/ http://www.seqahead.eu

35 ALLBIO 10 partners 8 countries FP7 project Broadening the Bioinformatics Infrastructure to unicellular, animal, and plant science www.allbioinformatics.eu

36 THANKS!! Como 2012


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