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Hi @maickrau,
I'm trying to map Nanopore R10 and Hifi reads to the HPRC graph and its super slow- I'm mapping 1 million reads on 64 threads and it still hasn't finished after 20 hours. Is this what…
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We are now working on Nanoseq in a monkey. Human and mouse chromosomes usually start with N. But, in this monkey, some chromosomes start with ATGC. When sequence reads are mapped to the end of such ch…
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The usage report printed by "rgi bwt -h" shows the only available options to be for paired end illumina reads.
Is there any flag to feed it single ONT sequenced metagenomic reads?
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If you’re using VoiceOver and {{VO + Arrows}} to navigate individual content, the variant selectors in QuickView are read twice. If you pause after, it will also read out what I assume is a string of …
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Hi,
I have Pacbio FLNC reads in fastq format. What options should be specified while running the tool. I was thinking
`--data_type pacbio --fl_data`. Is this correct?
Thanks
Abhijit
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I am using the kraken2 + Bracken technique route. In kraken2's result file ".k2report ", the reads of one species read around 1000, while in bracken's processed ".braken "file, the reads of that speci…
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Tracking issue for bounded staleness reads, as outlined in #66020.
The tracking issue is split into [three stages](https://github.com/cockroachdb/cockroach/blob/025c53decd8eb00cb70a1d410692026c9f86…
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Hello!
I wonder if you could let me know what tags the remapped BAM should be equipped with.
I want to customize some parts of the source code so that svviz2 may remap reads with the mappers o…
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Hello,
I am trying to compare the performance of different mappers on long reads and minigraph has unexpectedly low accuracy. I'm mapping 1 million simulated HiFi and R10 reads to the [HPRC](https:…