New Statistical Algorithms for the Analysis of Mass - FU Berlin, FB MI ...
New Statistical Algorithms for the Analysis of Mass - FU Berlin, FB MI ...
New Statistical Algorithms for the Analysis of Mass - FU Berlin, FB MI ...
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172 CHAPTER 8. CONCLUSION AND <strong>FU</strong>TURE DIRECTIONS<br />
<strong>the</strong>se judgements, should be replaced by multi-source (or multi-dimensional)<br />
biomarkers that combine in<strong>for</strong>mations from different sources in a reasonable<br />
way.<br />
What we call a bioprint is <strong>the</strong> multi-dimensional extension <strong>of</strong> <strong>the</strong> biomarker<br />
concept. Using many different data sources (-omics) and different analyzing<br />
techniques, bioprints can be created that not only rely on a single change but<br />
ma<strong>the</strong>matically and biologically meaningful combine many different relevant<br />
elements. These potentially complex models require not only sophisticated<br />
data-mining algorithms <strong>for</strong> <strong>the</strong> analysis but also large amounts <strong>of</strong> computing<br />
power.<br />
The ultimate goal should be to find disease specific bioprints using data<br />
from all available kinds <strong>of</strong> sources and examine <strong>the</strong> relationships between clinical<br />
symptoms and genetic, biochemical, immunological and cellular biomarkers.<br />
This and perhaps only this would facilitate an area <strong>of</strong> personalized<br />
medicine: “Although <strong>the</strong>y are certainly related, <strong>the</strong> only way to really achieve<br />
personalized medicine is to be able to create an in<strong>for</strong>mation base that lets you<br />
say what is it about an individual that I need to know in order to define what<br />
<strong>the</strong> right treatment is.” (Carol Kovac, General Manager Healthcare and Life<br />
Sciences at IBM interviewed by (McDonald, 2006).)<br />
The Next Steps<br />
We feel that <strong>the</strong> <strong>the</strong>re are four main steps that have to be taken in order to<br />
come closer to <strong>the</strong> aim <strong>of</strong> providing such an in<strong>for</strong>mation base:<br />
1. Evaluate available data: Collect, classify and analyze publicly available<br />
biobank data and data available in “un<strong>of</strong>ficial biobanks” such as<br />
hospitals or institutes.<br />
2. Consolidate compatible data on a disease level: Based on <strong>the</strong><br />
analysis in <strong>the</strong> previous step, data clusters are created that are related to<br />
<strong>the</strong> focused cancer types. Subsequently, sub-clusters are extracted that<br />
contain compatible data, that is, data that can reasonably be compared<br />
with respect to biology.<br />
3. Data Mining: Develop algorithms to analyze and mine this data.<br />
4. Web-based community access: Build and provide an “out-<strong>of</strong>-<strong>the</strong>box”<br />
web-based plat<strong>for</strong>m <strong>for</strong> researchers across disciplines and medical<br />
staff to access this data and per<strong>for</strong>m individual analyses.<br />
The ultimate goal: Value <strong>for</strong> Healthcare<br />
By developing new ways to identify major diseases at <strong>the</strong> molecular level and<br />
provide appropriate (personalized) diagnosis and <strong>the</strong>rapeutics. This means<br />
shorter duration <strong>of</strong> <strong>the</strong>rapy, increased healing chances and <strong>the</strong>re<strong>for</strong>e increases<br />
life quality.