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Hi Job,
I'm getting some weird output in my sci-dash:
- The Total Input Reads column adds up to more than the Total input read-pairs
- Many cell metrics (mean reads/cell, mean UMI/cell, etc) ar…
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From Allison Heath and Eric Wenger:
Good morning, quick question on what the Ontology WG recommends for c2m2 OBI id's in several cases where we are not seeing matches.
Kids First data has several…
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**Is your feature request related to a problem? Please describe.**
I would like to be able to quickly determine what research article I should reference simply from looking at the output of `datasets…
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Hello!
I have obtained three graph pan-genomes through three software: Minigraph, Minigraph_cactus and Pggb, which contain 12 mammalian species. Then I also have nearly 500 next-generation sequencing…
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Hi,
I would like to know if the command _nanopolish eventalign_ changes the file size/content of the sequencing_summary file we specify in the command. If so, why? Since we are not writing the out…
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Dear Gao Xue,
Recently I'm studying your publication "Long read genome assemblies complemented by single cell RNA-sequencing reveal genetic and cellular mechanisms underlying the adaptive evolution…
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## WGS (Whole Genome Sequencing)
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Hi, I'm a new to cnvkit. Thanks for this excellent tool. As it was pointed out in the documentation, CNVkit is primarily designed for use on hybrid capture sequencing data, where off-target reads are …
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Hi.
When I performed a de novo assembly using HIFI, I obtained a genome size of 1.7 Gb. Since there was no prior information available about my sample, I decided to estimate the genome size. When …
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**Describe the bug:**
The activation command for `fish` fails for me because there is a `(...)` in the pathname, which `fish` tries to run as a command substitution since the command run by `flox a…