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A bioinformatics tool for working with modified bases

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Hello, I am working on quantifying the ratio of 4mC in mouse samples, but I have encountered a challenge. According to public papers, 4mC is very rare in mammals. I...

question

I am trying to merge two bedmethyl files, each produced from 2 different samples, using this command modkit bedmethyl merge sample_a.bed.gz sample_b.bed.gz > merged.bed I get this error error: unrecognized...

troubleshooting

@rmp When I want to perform m6A analysis and use `modkit pileup` to identify methylation information, should I specify the reference genome or the reference transcriptome with the `--ref `...

question

@ArtRand @rmp Hey, I received a file named pass.fq.gz, which the company called using Dorado. I then mapped the reads from the .fq.gz file to the transcriptome, when I run...

question

Hi, Awesome tool!. Could we have a feature similar to deeptols computeMatrix for creating metagene profiles of modification pattern. Thanks. Regards, Kamal

enhancement

FEATURE REQUEST: Extract/Calls reports number of CpG's covered in the sample It would be awesome if one was using a motif file to have the percent of CpG's covered in...

https://nanoporetech.github.io/modkit/intro_repair.html Commands provided in link above to sort BAM files using samtools prior to repair seem to be missing 'sort': the two BAM files need to be sorted samtools -n...

documentation

Hello, I am working with plant DRS dataset I ran the command (for m6A all context) $dorado basecaller rna004_130bps_sup\@v5.0.0 c6_r1/pod5/ --modified-bases-models rna004_130bps_sup\@v5.0.0_m6A\@v1/ --device cuda:all > c6_r1_sup_m6A.bam and then pileup using...

question
troubleshooting

Pls look into this error and suggest how to resolve it? Here: 1. I have indexed .bam (from dorado) and then converted to fasta (reads). 2. reference: assembled (genome: NCBI)...

troubleshooting

# 1- I want to make differential methylation anlysis between these samples, I thought I should use that command mentioned in the tutorial modkit dmr multi \ -s ${norm_pileup_1}.gz norm1...

question