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visualization the data #78
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Hi @Fatihlrcfs , thanks for your interest of out tool. The methylation frequency file in bed/bedmethyl fomat (generated by scripts/call_modification_frequency.py with However, currently deepsignal doesn't support per-read modification visualization. Maybe there is a way to convert the .call_mods.tsv (per-read outputs) file of deepsignal (with the raw BAM file) to modBAM format, which can be visualized by genome browsers and Methplotlib (Ref: https://mobile.twitter.com/adrienleger2/status/1395400611869429762). But I haven't tried it yet. Another way, which may be similar to modBAM, is to create a bisBAM file (BAM file for IGV in Bisulfite mode) using the per-read outputs of deepsignal and the raw BAM file, where all unmethylated C/Gs are converted to T/As. Vahid, the author of NanoMethPhase, wrote some code for this (it supports converting nanopolish/tombo/deepsignal per-read outputs to bisBAM file, ref: https://github.com/vahidAK/NanoMethPhase/blob/iss5/nanomethphase/main.py#L631). However, the code/pipeline may need some changes, as it was designed for haplotype-aware methylation. Best, |
Hi @PengNi , Kind Regars. |
hi @PengNi , |
Hi @Fatihlrcfs , to run |
Hi @PengNi many thanks for quick response. have a great days:) |
Hi dear,
firstly thank you for providing Deepsignal. I am wondering how can ı visualize the output of Deepsignal? could you offer any package or guideline in order to visualize the output data? Also, I am currently working on the output of Nanopolish with Methyplotlib and Nanomethvis packages and is there any way to transform the output of Deepsignal to the suitable format of Methplotlib/ Nanomethviz. many thanks.
Kind Regards.
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