fCNV | probabilistic method for non-invasive analysis | Genomics library
kandi X-RAY | fCNV Summary
kandi X-RAY | fCNV Summary
a probabilistic method for non-invasive analysis of de novo CNVs in fetal genome based on maternal plasma sequencing.
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Top functions reviewed by kandi - BETA
- Evaluate a function on the given samples .
- Perform extended labeling .
- Compute the Backward algorithm .
- Estimate ground truth .
- Compute the evaluation for a given reference .
- Reads a plasma file .
- Recursively pile up read up .
- Compute statistics for all problems .
- get line from file
- compute upper bound
fCNV Key Features
fCNV Examples and Code Snippets
Community Discussions
Trending Discussions on fCNV
QUESTION
I have multiple cnv
files and I would like the plot the temperature variable from each file onto one plot. I have a loop to open the multiple files however, when I plot it, it plots each dataset on a new plot so I end up with multiple figures instead of one.
Here is the script:
...ANSWER
Answered 2017-Oct-25 at 13:33You are creating a new plot with each iteration of your for
loop. Bring the plot creation outside of the loop.
Community Discussions, Code Snippets contain sources that include Stack Exchange Network
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No vulnerabilities reported
Install fCNV
You can use fCNV like any standard Python library. You will need to make sure that you have a development environment consisting of a Python distribution including header files, a compiler, pip, and git installed. Make sure that your pip, setuptools, and wheel are up to date. When using pip it is generally recommended to install packages in a virtual environment to avoid changes to the system.
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