Tang JIWEI
Tang JIWEI
@ArtRand `modkit dmr pair -a Y1_5_1_m6A.bed.gz -a Y1_5_2_m6A.bed.gz -b Y2_5_1_m6A.bed.gz -b Y2_5_2_m6A.bed.gz -o Y5dm.bed --header --ref transcripts.fa --segment Y5single_base_segments.bed --base A -t 30 --log-filepath Y5dm.log --careful`  `mod_kit 0.4.5` `tabix...
 `modkit pileup Y1_5_1.bam Y1_5_1.bed --ref transcripts.fa --log-filepath Y1_5_1.log -t 20 --with-header`  `modkit pileup Y1_5_1.bam Y1_5_1_m6A.bed --ref transcripts.fa --log-filepath Y1_5_1_m6A.log -t 30 --with-header --ignore 17596` https://github.com/nanoporetech/modkit/issues/347 @ArtRand 1.Why is...
@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 `...
@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...
@Psy-Fer Hi, when I run this command:`blue-crab p2s 20241127-DRS1499-PAY10858-P02.pass.pod5 -o 20241127-DRS1499-PAY10858-P02.pass.blow5 -t 20` there are errors : 07-Jan-25 17:10:51 - blue-crab - [ERROR]: acquisition_id does not match prev value: 0:...
@satta Hi, The latest ONT RNA004 original file of my DRS data is POD5. How can I use nanopolish to build an index? please
@lh3 @chhylp123 @molecules Hi, The genome is 2.5 Gb in size, with a heterozygosity of 6.9% and 90% repetitive sequences (a highly repetitive species). Although both HiFi and Hi-C data...
Hi @EduEyras @leipzig The data I used is ONT DRS data, there are 2 species (cultivar and wild species, uniformly aligned to the cultivar genome) with 2 replicates and a...
Hi @leipzig @EduEyras Here I'm trying to do it in samples to get the GTF for each sample, but it keeps reporting this error `ERROR:__main__:Unknown error: (, IndexError('list index out...