Comments (2)
No, that's calculated by igv.js on the fly. So it will show in the jigv plot but it's not readily availble to write to text. you can use a pileup tool or a variant caller at specific loci to extract allele depths for given sites.
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yes, pysam can do such work, but not that fast, because mosdepth is so fast, so I wonder if you prepare to add this function into jigv
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Related Issues (20)
- Read sequence is "*" HOT 1
- Windows build HOT 1
- Anotation track HOT 4
- Add bed-format file to sites option?
- Provide small example output HOT 2
- parameter usage for RNA sequencing samples HOT 2
- Custom Template HOT 1
- IDEA: seeing reads for more than one sample without pedigree file HOT 4
- jigv settings for targeted deep sequencing HOT 4
- automatic taking images given list of regions HOT 1
- show SAM flag on click of alignment
- Empty output html HOT 1
- vcf sites html does not show alignments HOT 4
- possible to display gene name by default? HOT 3
- customization
- sort by base HOT 3
- Should print help when no input provided? HOT 1
- Security: users with access to the same server can see each others sessions HOT 2
- Feature request: find read by name and highlight/color specific read(s) HOT 2
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