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Mini16S protocol is a newer protocol that reduces cost and time. It is not currently supported by LabControl.
This description is a placeholder issue to be fleshed out at a later date.
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Hello, I recently performed a de novo genome assembly using HiFiasm.
And I have Hifi sequencing data.
First, thank you let us use this wonderful tool.
But when i run for the first time,
I got lo…
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casey was loading [PRJDB4532](https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJDB4532). no biosample is loaded because its not linked to the project in the returned XML.
Maybe we want to be able t…
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### Description
I would like to propose a new feature for Apache Airflow: the ability to assign a pool to an entire task group, enabling better control over the execution of tasks within the group. T…
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Hi Ben and team,
I am currently working on two sets of data that I have received elsewhere, both from the V4 region. For the first dataset, I have both forward and reverse reads prior merging (2x15…
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There are 3 types of libraries we made
1. cleavage pool (3 replicate libraries) - 7658 cells
2. blastula (1 library) - 2836 cells
3. gastrula (4 replicate libraries) - 18511 cells
The cleavage p…
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Hi,
Is it possible to run scFBA without including pooled/bulk RNA-seq data? (Because sometimes this data is not available).
From your README file, it seems that it is possible to run scFBA without…
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GanttStart: 2023-04-20
### Background
In https://github.com/rasilab/github_demo/issues/3 and https://github.com/rasilab/rqc_aggregation_aging/issues/101, we identified and validated FK as a stalling…
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e.g.
cwl.metrics.parser.py -wgs -w 2859352
put in 20 as the metric to judge:
report says this below:
QC Pass Metrics
(samples must meet all requirements)
**HAPLOID COVERAGE: 20 (User defined)…
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Hi,
I’m working with scRNA-seq data where three samples are pooled together and we have 20 pools. I used souporcell for demultiplexing without initial whole-genome sequencing SNP data (as it wasn’t…