Tang JIWEI

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@sanyalab Hi, If you just wants to construct a relatively complete full-length transcriptome, I think it is possible to do so.

@ArtRand Thank you! The dorado step was performed by a partner company. However, I still have a question. I have two species, which are allotetraploids belonging to the same genus....

@ArtRand Thank you for your patient reply! I have another question: The pass.fq.gz file provided by the sequencing company already contains methylation modification information and polyA tail length. Can I...

Hi @ArtRand the BAM file generated from aligning sequencing reads to a transcriptome I have a doubt regarding the following commands: Without using --ref: `modkit pileup Y2_5_2.bam Y2_5_2.bed --log-filepath Y2_5_2.log...

@ArtRand Regarding the filtering of positions based on `percent_modified`, I have set a threshold of >20%. Is there any published or commonly accepted justification for using this threshold? ![Image](https://github.com/user-attachments/assets/048c807e-352b-4c8e-a635-27e31cbffe8d) Secondly,...

@hasindu2008 hi, so Can f5c also calculate polyA length?

@hasindu2008 Okay ,thank you! If it is RNA004, what methods can be used to calculate the polyA length?

@hasindu2008 Yes, But this step is coducted by sequecing company, because I don't have GPU. Okay, thank you again!

Sorry, It's my carelessness

@XqKang If the data you are using is ONT RNA004, I suggest you use dorado+modkit, nanopolish does not support POD5, you need to convert POD5 to BLOW5