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[WIP] Outline the Study section #136
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tag citation | ||
Zhou2015_deep_sea doi:10.1038/nmeth.3547 | ||
Chen2015_trans_species doi:10.1093/bioinformatics/btv315 | ||
Arvaniti2016_rare_subsets doi:10.1101/046508 | ||
Angermueller2016_single_methyl doi:10.1101/055715 | ||
Shaham2016_batch_effects arxiv:1610.04181 |
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## How is deep learning used to study basic biological processes in a manner that may provide future insights into human disease? | ||
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*The (awkward) placeholder section title is intended to help define the scope. | ||
We do not want this section to become a miscellaneous collection of everything | ||
that does not fit in Categorize and Treat.* | ||
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*One proposal is that we organize this roughly by what is being predicted, | ||
which will generally correspond to the types of data being used. For each | ||
sub-section we can quickly introduce the prediction problem and cite some | ||
examples of the relevance to disease. Hypothetically, if we had an algorithm | ||
that produced perfect predictions on the task, what would we learn and how | ||
could those predictions be used?* | ||
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*Existing reviews could be mentioned briefly.* | ||
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*It may not fit here, but there could be a general discussion of why different | ||
neural network architectures are particularly well-suited for different types | ||
of input data. For example, CNNs and RNNs for 1-dimensional data are used | ||
in several categories below.* | ||
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*A few suggestions for sub-sections follow. Some of these could be left out | ||
because our goal is not an exhaustive enumeration of methods. Some | ||
are important areas of biology, but there may not be much deep learning- | ||
specific content to present. Others may be important areas where we lack | ||
expertise, in which case we may acknowledge the application area but not | ||
dive into merits or weaknesses of individual methods.* | ||
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### Gene expression | ||
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*Predicting gene expression levels and unsupervised approaches for learning | ||
from gene expression. Those could be divided into separate sub-sections.* | ||
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### Splicing | ||
There was a problem hiding this comment. Choose a reason for hiding this commentThe reason will be displayed to describe this comment to others. Learn more. I like splicing as separate from gene expression, unless we change things to "transcript expression" |
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*A separate section from general gene expression section above.* | ||
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### Transcription factors and RNA-binding proteins | ||
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*Existing reviews have covered some of these papers rather well and we do not | ||
want to repeat what has already been well-stated elsewhere. This could | ||
be split into two sub-sections or kept very brief.* | ||
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### Promoters, enhancers, and related epigenomic tasks | ||
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*We may want to be selective about what we discuss and not list every | ||
application in this area.* | ||
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### Micro-RNA binding | ||
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*miRNAs are important biologically, but have neural networks produced anything | ||
particularly notable in this area?* | ||
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### Protein secondary and tertiarty structure | ||
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*We have not surveyed this area comprehensively yet.* | ||
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### Signaling | ||
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*There is not much content here. Can [@tag:Chen2015_trans_species] be covered | ||
elsewhere?* | ||
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### Cellular phenotypes | ||
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*These are primarily imaging-based phenotypes. We have not surveyed this area | ||
very comprehensively. We could decide to not make imaging a primary focus, | ||
refer to existing reviews, and mention only a few particularly noteworthy | ||
representative papers. Alternatively, we need to expand our literature review | ||
and summaries immediately if someone wants to be responsible for this | ||
sub-section.* | ||
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*Transfer learning from non-biological datasets to biological imaging | ||
data could fit here, and that does seem like an important topic. Or | ||
transfer learning could be a more general topic for the Discussion section.* | ||
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### Single-cell | ||
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*There are not many neural network papers in this area (yet), unless we count | ||
imaging applications. But there is still plenty to discuss. The existing | ||
methods [@tag:Arvaniti2016_rare_subsets @tag:Angermueller2016_single_methyl] | ||
use interesting network architectures to approach single-cell data. | ||
[@tag:Shaham2016_batch_effects] could fit here.* | ||
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### Metagenomics | ||
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There was a problem hiding this comment. Choose a reason for hiding this commentThe reason will be displayed to describe this comment to others. Learn more. Do you want to update this to confirm that there will be a section? @gailrosen has sufficient content to fill out a section. |
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*@gailrosen will write this* | ||
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### Sequencing and variant calling | ||
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*We have one nanopore paper in the issues and very recent work on variant calling | ||
that looks worthy of inclusion.* |
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If you want to assign these bits out like you did with the metagenomics section, you can assign this and splicing to me. I may see if we can snag a splicing guru from Penn (Yoseph Barash). If not, I did read a few of those papers and could write that bit.