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mscook / SeqFindR

A tool to easily create informative genomic feature plots
http://mscook.github.io/SeqFindR/
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Shading = level of similarity #4

Closed bawee closed 10 years ago

bawee commented 11 years ago

An option to represent higher sequence similarity as darker shades and lower similarity as lighter shades would be very informative.

bawee commented 11 years ago

A way of visualising a low coverage (e.g. < 70%) of the hit found in the assemblies will also be useful to highlight significant but incomplete hits.

These incomplete hits could represent pseudogenes or miscalled genes.

mscook commented 10 years ago

SeqFindR is only really for presence absence. While this may be possible, I do not have it in the plans. Labelling this as won't fix and closing.