Convert Annotation Track Coordinates converts annotation coordinates, either from hg19 coordinates to hg38 coordinates, or vice versa. This remapping of coordinates, also referred to as 'liftover', makes use of the NCBI Remapping Service (https://www.ncbi.nlm.nih.gov/genome/tools/remap). Network access is therefore necessary to use this tool.
To run Convert Annotation Coordinates Track, go to:
Tools | QIAseq Panel Expert Tools () | QIAseq DNA Panel Expert Tools () | Convert Annotation Track Coordinates ()
The tool takes annotation tracks, typically primer tracks or target region tracks, as input (see figure 6.42).
In the next step, a target reference must be selected (see figure 6.43). If the annotation track used as input was based on an hg19 reference, select an hg38 reference genome. If the annotation track used as input was based on an hg38 reference, select an hg19 reference genome. If not already available, a copy of the relevant target reference can be downloaded using the Reference Data Manager.
Under settings you can choose to use the Use second pass alignments option that allows alignment to duplicated sequences. For more information about second pass alignment, please see https://www.ncbi.nlm.nih.gov/genome/tools/remap/docs/whatis and https://www.ncbi.nlm.nih.gov/genome/tools/remap/docs/alignments.
This tool outputs an annotation track with coordinates based on the target reference and a report. If the remapping was done without selecting the Use second pass alignments option, the report will typically list the potentially skipped intervals, that is, the annotations that could not be mapped to coordinates of the selected target reference.
If remapping was done with the Use second pass alignment option selected, the report lists Skipped intervals, Annotations with multiple intervals that were split because not all intervals could be remapped and Duplicated intervals. The duplicated intervals table lists multiple outputs for the same input, which means that the report will have multiple entries for the same chromosome, name, and interval as shown in figure 6.44.
If multiple outputs were generated for some of the annotations, it possible to manipulate the resulting Annotation Track. This can be done by opening the output file with the extension (Converted) in table view and then choosing the subset of the output annotations track that is of relevance by selecting the relevant rows and clicking on the button labeled Create Track from Selection.