metaseq
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Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data
Metaseq
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Briefly, the goal of metaseq
is to tie together lots of existing software into
a framework for exploring genomic data. It focuses on flexibility and
interactive exploration and plotting of disparate genomic data sets.
The main documentation for metaseq
can be found at https://daler.github.io/metaseq.
If you use metaseq
in your work, please cite the following publication:
Dale, R. K., Matzat, L. H. & Lei, E. P. metaseq: a Python package for
integrative genome-wide analysis reveals relationships between chromatin
insulators and associated nuclear mRNA. Nucleic Acids Res. 42, 9158–9170
(2014). http://www.ncbi.nlm.nih.gov/pubmed/25063299
Example 1: Average ChIP-seq signal over promoters
Example 1 <https://github.com/daler/metaseq/blob/master/doc/source/example_session.ipynb>
_ walks you
through the creation of the following heatmap and line-plot figure:
.. figure:: demo.png
Top: Heatmap of ATF3 ChIP-seq signal over transcription start sites (TSS) on
chr17 in human K562 cells. Middle: average ChIP enrichment over all TSSs
+/- 1kb, with 95% CI band. Bottom: Integration with ATF3 knockdown RNA-seq
results, showing differential enrichment over transcripts that went up,
down, or were unchanged upon ATF3 knockdown.
Example 2: Differential expression scatterplots
Example 2 <https://github.com/daler/metaseq/blob/master/doc/source/example_session_2.ipynb>
_ walks
you through the creation of the following scatterplot and marginal histogram
figure:
.. figure:: expression-demo.png
Control vs knockdown expression (log2(FPKM + 1)) for an ATF3 knockdown
experiment. Each point represents one transcript on chromosome 17.
Marginal distributions are shown on top and side. 1:1 line shown as
a dotted line. Up- and downregulated genes determined by a simple 2-fold
cutoff.
Other features
In addition, metaseq
offers:
-
A format-agnostic API for accessing "genomic signal" that allows you to work with BAM, BED, VCF, GTF, GFF, bigBed, and bigWig using the same API.
-
Parallel data access from the file formats mentioned above
-
"Mini-browsers", zoomable and pannable Python-only figures that show genomic signal and gene models and are spawned by clicking on features of interest
-
A wrapper around pandas.DataFrames to simplify the manipulation and plotting of tabular results data that contain gene information (like DESeq results tables)
-
Integrates data keyed by genomic interval (think BAM or BED files) with data keyed by gene ID (e.g., Cufflinks or DESeq results tables)
Check out the full documentation <https://daler.github.io/metaseq/>
_ for
more.