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Feature request: filtering of tracks (particularly alignment) #1606
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I'm not entirely sure I understand what you mean by "filter". Do you want to filter reads from the bam file? The reference to genes in a gff3 is confusing, I'm not sure what that has to do with reads in the file. If you want to look at specific loci of course that is supported. Perhaps a screenshot would help, or a detailed description of what you are currently doing would help. Or both. |
Apologies, I was trying to abstract the feature over different tracks while describing it which made the whole thing confusing. I'll break it up into a couple versions. Filtering reads while displaying an alignment trackIn a single-cell experiment we'll have reads from many different cells at a given locus. If I only want to look at the reads from a specific cell, I could make a new BAM that only has reads with a certain In the context of long-read transcriptomics, a common thing I've been doing is to look at the various transcripts predicted for a particular gene, and inspect the read support for each one. Sometimes the software will construct a "novel" transcript but a lot of evidence is ambiguous (like, a single exon) and we don't trust that so much. There can be lots of transcripts in the constructed annotation, so it's useful to filter to only the specific isoform when inspecting it. Right now I make a new BAM file for that. Alternatively I can put the isoform assignment info into a BAM tag and sort on that tag, but the visualization is less clean because it will fit in other reads where it can. Filtering transcripts from an annotation trackThis is maybe more of a niche, but again relates to deriving novel transcript annotations from long-read data. Depending on the software used, there can be a lot of isoforms identified. I've found it useful to filter that down to the subset with a large number of counts (many isoforms are represented by a single read and I doubt they're real). A filter tool could work in this context as well, if e.g. I customized the annotation file with additional metadata, to filter to isoforms with a count above some threshold. Or I could filter on the name to only look at known or novel isoforms. I think the BAM filtering is more clearly useful, but I'm not familiar with the architecture of igv.js and thought it might be possible to build a more generic filtering widget. |
OK, got it. Filtering could be static, specified in the track configuration and applied when the file is read, or dynamic from a menu (as sorting or coloring is currently done). I assume dynamic would be more useful for your case, correct? Static might be easier to implement. Both are probably useful. I'm just gather information, not sure when I will get to this. |
Yeah dynamic would be best because we could look at multiple cases in the same session without reloading. But static is still nice, it's basically just replacing a manual step where I make the BAM myself.
No worries! It's kind of a niche feature for sure but it'd be helpful for our visualization. I might look into the code myself to see if I can figure out where this could fit in, but I'm not a JS expert. |
There's another concept from IGV-desktop, not implemented in igv.js yet, that might be useful here -- grouping. Then you could group alignments, for example, by CB:Z or other tag. |
I've found igv.js and igv-notebook to be super useful for visualizing novel transcriptomes and the read support for them. One thing that I've repeatedly found myself doing: I take the input for a track I've visualizing (could be a gff3, genePred, BAM, etc) and filter it down to a specific subset so that it's easier to visualize e.g. only certain genes in the gff3, or only reads that map to a specific transcript, and so on.
It would be amazing if I could do this in the igv.js browser, or via a callback in my notebook. Being able to write a custom callback is more powerful, but I don't know how complex it would be to implement. But just the ability to filter by exact match for a given field (or BAM tag) would still be very useful.
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