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A bioinformatics tool for working with modified bases

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Hello and thanks again for the great tool. We've run open chromatin predict and obtained bedGraphs, which we've converted to bigWigs and visualized in IGV. These look great in areas...

troubleshooting

Hi, @ArtRand First, thank you for developing such a useful tool. I have a question about the definition and behavior of "skipped reads" when using the modkit extract full command....

question

Thanks for developing this useful tool. I am having trouble on Open Chromatin Predict(modkit open-chromatin predict). The output always stop writing at some point and I receive no error message....

troubleshooting

I'm running modkit extract calls (v0.5.0) on some very large bams on my HPC, and it seems to be failing out with an OOM even if I have 50GB of...

troubleshooting

When calling DMRs with the `--segment` option I notice a lot of overlap in my samples between two different tests. By that I mean I looked at differential methylation across...

enhancement

I have a PCR fragment with defined Methylation percentages. For this issue, lets focus on 0% methylated. Goal is to be able to accurately measure the input Methylation Percentage (here...

question

`test_pileup_with_header` and `test_pileup_no_filt` write to the same file: https://github.com/nanoporetech/modkit/blob/8fa79e3e55c5735637f9ea3115c3e621b58fd74c/tests/test_pileup.rs#L24 https://github.com/nanoporetech/modkit/blob/8fa79e3e55c5735637f9ea3115c3e621b58fd74c/tests/test_pileup.rs#L901 Same here: https://github.com/nanoporetech/modkit/blob/8fa79e3e55c5735637f9ea3115c3e621b58fd74c/modkit/tests/test_pileup.rs#L922 This leads to test failures when tests are run in parallel. Workaround: ` cargo test --profile=release --...

bug

Hello everyone, **code used: `./modkit extract calls calls.bam calls.tsv --reference ref.fasta`** I am analyzing modification calls with Modkit. When I view my aligned BAM file in IGV, I see good...

question
troubleshooting

Hello, I ran multiple replicates of the modkit pileup step using the same input BAM file and same reference genome, changing only the number of threads: Data: Same sample, same...

bug

Dear Team, Can I use "haplotagged.cram" (output of wf human variation pipeline) as an input to "modkit entropy" ?

enhancement