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Related discussions:
- #8
- #17
- #5
# History
For years we've debated the question of whether sequence collections would be ordered or unordered. In #17 we determined that the digests **w…
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CWL allows to describe tools/pipelines/workflows and enhances reproducibility. Hoverer, describing is not only about how to run or technical info about execution environment but also about what this …
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I think epic2 is for regular peak calling (e.g., TF-chip vs. input)? epic2-df is for differential peak calling (treatment vs. control)? Then what is epic2-bw for?
Thanks,
Yichao
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(CC @ymen. Thanks to @timjph for initially bringing this to my attention).
The new translation code is sometimes generating incorrect (or at least improbable) translations in cases where gene annota…
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The new great Blast service at BV-BRC generates a downloadable output CSC or text table, but it is empty. I checked any times
![empty_blast_output_BV-BRC](https://user-images.githubusercontent.com/…
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#### Feature Request Description
I'm not sure if this is a feature request or a bug report. That answer is contingent on whether anonymous (non-SAS) access to Azure Storage blobs is supported.
###…
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Hi Teri,
I have been teaching this week and have had a couple of requests. Firstly, can we provide a link to the Ensembl genome browser. I think this is reasonable.
Second, can we link directly …
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I like the `Wiggle` object a lot. I tried modeling wiggle data by creating length-1 `Feature` objects in the ADAM schema, but it's obviously less efficient.
One issue, though, is that performing int…
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Thanks for this great tool.
When multiple annotations are too close together (like within 10000 bases) in one chromosome as shown in , only one of them could be visible. Is there any way to zoom i…
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_From @TomKellyGenetics on September 1, 2015 23:18_
Hi team, I thought this would be a good space to start planning ideas for SYSKA topics to gauge interest in various things we could do... and find …