I am on section 3.7 of Chollet's book Deep Learning with Python. The project is to find the median price of homes in a given Boston suburbs in the 1970's.
At section 'Validating our approach using K-fold validation' I try to run this block of code:
I get an error KeyError: 'val_mean_absolute_error'
I am guessing the solution is figure out the correct parameter to replace val_mean_absolute_error. Adobe flash player 11 mac. I've tried looking into some Keras documentation for what would be the correct key value. Anyone know the correct key value?
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To get a feeling for what deepTools can do, we’d like to give you a brief glimpse into how we typically use deepTools for ChIP-seq analyses. For more detailed exampes and descriptions of the tools, simply follow the respective links.
Note
While some tools, such as plotFingerprint, specifically address ChIP-seq-issues, the majority of tools is widely applicable to deep-sequencing data, including RNA-seq.
As shown in the flow chart above, our work usually begins with one ormore FASTQfile(s) of deeply-sequenced samples. After preliminary quality control usingFASTQC,we align the reads to the reference genome, e.g., usingbowtie2.The standard output of bowtie2 (and other mapping tools) is in the form of sorted and indexed BAM filesthat provide the common input and starting point for all subsequent deepTools analyses.We then use deepTools to assess the quality of the aligned reads:
- Correlation between BAM files (multiBamSummary and plotCorrelation).Together, these two modules perform a very basic test to see whetherthe sequenced and aligned reads meet your expectations. We use thischeck to assess reproducibility - either between replicatesand/or between different experiments that might have used the sameantibody or the same cell type, etc. For instance, replicates shouldcorrelate better than differently treated samples.You can also assess the correlation of bigWig files using multiBigwigSummary.
- Coverage check (plotCoverage). To see how many bp in the genome are actually covered by (a good number) of sequencing reads, we use plotCoverage which generates two diagnostic plots that help us decide whether we need to sequence deeper or not. The option
--ignoreDuplicates
is particularly useful here!
For paired-end samples, we often additionally check whether the fragment sizes are more or less what we would expected based on the library preparation. The module bamPEFragmentSize can be used for that.
- GC-bias check (computeGCBias). Many sequencing protocolsrequire several rounds of PCR-based DNA amplification, which often introduces notable bias, due to many DNA polymerases preferentially amplifying GC-rich templates. Depending on the sample (preparation), the GC-bias can vary significantly and we routinely check its extent. When we need to compare files with different GC biases, we use the correctGCBias module.See the paper by Benjamini and Speed for many insights into this problem.
- Assessing the ChIP strength. We do this quality control step to get afeeling for the signal-to-noise ratio in samples from ChIP-seqexperiments. It is based on the insights published by Diaz etal.
Once we’re satisfied with the basic quality checks, we normally convertthe large BAM files into a leaner data format, typicallybigWig.bigWig files have several advantages over BAM files, mainly stemmingfrom their significantly decreased size:
Deeper 2019 Movie
- useful for data sharing and storage
- intuitive visualization in Genome Browsers (e.g.IGV)
- more efficient downstream analyses are possible
The deepTools modules bamCompare and bamCoverage not only allow for simple conversion of BAM to bigWig (or bedGraph for that matter), but also for normalization, such that different samples can be compared despite differences in their sequencing depth.
Finally, once all the converted files have passed our visual inspections (e.g., using the Integrative Genomics Viewer), the funof downstream analysis with computeMatrix, plotHeatmap and plotProfile can begin!
Deeper 2019 Full Movie
deepTools Galaxy. | code @ github. |