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Hi,
I am trying to assemble the genome of a worm, and I was hoping that minipolish would detect the mitochondrial genome and output it in the gfa file.
I have sequencing one of my worm species a l…
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## *Repository Creation Request*
1. #### Coordinating Institute: Indian Institute of Technology Kharagpur
2. #### Approved Proposal: [Plant Metabolic Engineering Lab](https://drive.google.com/fi…
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Hello everyone,I'm trying to conduct a mapping of my 10x scRNA-seq data with a customized reference genome using STARsolo.My analysis seemed to work properly ("finished successfully" message appeared)…
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I have assembled few bacterial complete genomes using nanopore long reads via Unicycler bold module followed by multiple rounds of polishing by pilon using Illumina Miseq reads.
While submitting the…
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Dear Adam, Gil, and other developers,
Thank you very much for developing and maintaining LDhat. I was hoping you could help me with a couple of questions, and I hope this is the right place for tha…
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https://doi.org/10.1101/092890
> Next-generation sequencing (NGS) is a rapidly evolving set of technologies that can be used to determine the sequence of an individual's genome by calling genetic v…
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Hello @chhylp123
This is a very important piece of software.
Now I'm having some problems. I'm working in the plant direction and the material I'm using is a callus from some kind of woody pla…
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My experimental data is not whole genome sequencing but restriction site-associated DNA sequencing (RAD-seq), and I would like to know if I can use your software under such conditions.
Thanks again!
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**Describe the bug**
Dear bamtocov team,
I have human WES data and am trying to run bamtocov. After 6 hours, not even half is done/calculated, even when using 24 threads. Maybe I am missing somet…
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collecting references and annotations --
1. [VarCover: Allele Min-Set Cover Software](https://www.sciencedirect.com/science/article/abs/pii/S1525157819304143)
>To facilitate reference-material s…