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If Gosling already allows that, would be helpful to add the ability to show bases (in the read view) that are absent in reference genome. This makes it easy to identify reads which might be mis-mapped. If Gosling does not have such functionality, let's ignore for now.
From IGV, example of cleanly mapping region and one with likely misalignments.
The text was updated successfully, but these errors were encountered:
If Gosling already allows that, would be helpful to add the ability to show bases (in the read view) that are absent in reference genome. This makes it easy to identify reads which might be mis-mapped. If Gosling does not have such functionality, let's ignore for now.
From IGV, example of cleanly mapping region and one with likely misalignments.
The text was updated successfully, but these errors were encountered: