IGV RNAseq- Splice junction
Hi,
I'm a beginner in RNAseq. Hope someone with expertise in IGV can clear this out for me.
What can I infer with a splice junction of depth 1 and how exactly is the flanking width related to this splice junction?
chr1:11022241-11023192 Strand: + Depth = 1, Flanking Widths: (30,95)
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chr1:11022241-11023192 means the coordinate of the intron position (chromosome 1, position 11022241-11023192), and Depth = 1 means only one alignment supports this splice junction. I do not know how to interpret the flanking widths.
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