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```
What steps will reproduce the problem?
1. Compile the code attached and run it.
or
1. emit to a stream.
2. parse the stream.
3. read some but not all of the data in the stream from the parser/n…
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The DistSender circuit breakers from https://github.com/cockroachdb/cockroach/pull/118943 should possibly handle follower reads better. The two main cases are:
* A replica partitioned away from the…
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The current MTRDevice:
1. The read API requires nonnull endpointID, clusterID, and attributeID
2. The cache does not do wildcard search
This issue is to track support for wildcard reads.
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### What happened + What you expected to happen
I'm trying to create a Ray Dataset from a 300 GB JSONL file for offline inference. I expected Ray Data to read the file in a streaming fashion, but ins…
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Hi and first, thanks for the great work.
I tried to run Hostile to get the filtered result files and the removed read-pairs (Illumina paired-end data as input). What caught my eye is that the two r…
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I ran vaxrank 1.4.0 with a less strict threshold for RNA support (`--min-alt-rna-reads 1`) but that flag doesn't seem to get respected - the counts are correct in the Vaxrank report, ie it registers t…
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Hello,
I only have one fastq file for the sample. When running the amplicanPipeline function I get an error that my forward file is blank, but my forward file column contains the name of my fastq f…
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Hi
could you add more statistics for reads in your very useful tool?
- median read length
- minimal read length & maximal read length (read length range)
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Devise a way to handle very long reads (e.g. Oxford Nanopore).
Maybe make compatible with Minimap2 - as discussed by email with users. Alternatively, break up reads and process with Bowtie/Bowtie2
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CAn you possibly tell me the current default behaviour for chimeric reads if they are/could be multi-aligning reads as well. Can this be controlled,?