New release: MyGene.info Python client updated to v3.0.0

A few weeks ago, we released MyGene.info v3 API, which brings changes to exon field data structure and added accession version numbers to refseq and accession fields, along with some other back-compatible changes. Our Python client mygene module is now updated to use our v3 API as the default. We increased its version from v2.3.0 to v3.0.0, just to match the underlying API version. The mygene...
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New release: MyGene.info Python client updated to v2.3.0

Before the year-end holiday season of 2015, we released a new version of MyGene.info Python client ("mygene" Python module). Here is a summary of the the changes that were made in the new release (v2.3.0), and we encourage all of our users to upgrade to this new version. The upgrade is as easy as one line of command: pip install mygene -U To verify you have the latest version installed: In [1]:...
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MyVariant.py: our Python client for MyVariant.info services

We are happy to announce that the official Python client ("MyVariant.py") for our MyVariant.info web services is now available from PyPI (the Python Package Index). MyVariant.py allows users to annotate or query for human variants, either a single variant or a list of variants, without making explicit GET or POST web service calls. This is especially convenient for users who are already handling...
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MyVariant.py: our Python client for MyVariant.info services

We are happy to announce that the official Python client ("MyVariant.py") for our MyVariant.info web services is now available from PyPI (the Python Package Index). MyVariant.py allows users to annotate or query for human variants, either a single variant or a list of variants, without making explicit GET or POST web service calls. This is especially convenient for users who are already handling...
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Omics Pipe- computational framework for reproducible multi-omics data analysis

As mentioned on Monday, the researchers at the Su lab have been working diligently on a paper to introduce their new computational framework for reproducible multi-omics data analysis.  Advancements in sequencing technologies have made sequencing cheaper and more efficient, but this means that researchers need a way to handle all that data.  Different groups have generated a variety of tools for...
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