#Split in new chr1 145686997 148411223 #Split in new chr1 145808272 148411223 #Split in new chr10 46005406 49845537
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Matthew Speir
UCSC Genome Browser, User Support
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Hello, Emma.
Thank you for your follow-up question.
To import these overlaps into the UCSC Genome Browser, you can load your regions as a Custom Track:
1. Go to the Custom Tracks page for hg38: https://genome.ucsc.edu/cgi-bin/hgCustom?db=hg38 (also found under "My Data" > "Custom Tracks" in the blue bar menu).
2. Paste your regions in BED format into the text box, for example:
3. Click "Submit". You'll be taken to the Manage Custom Tracks page. From there, click "Go to first annotation" to view your regions in the genome browser.
In the session Matt shared previously, he also turned on two additional tracks set to "pack" to help illustrate why the liftOver was splitting:
LiftOver & ReMap - shows alignments from hg38 to the hg19 genome assembly, used by the UCSC liftOver tool and NCBI's ReMap service. More information: https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=liftHg19
Hg19 Diff - shows the differences between the hg38 and hg19 assemblies, indicating contigs (or portions of contigs) that are new to the hg38 assembly. More information: https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=hg38ContigDiff
You can find these under the "Mapping and Sequencing" track group on the browser graphic page and set their visibility to "pack".
I hope this helps. If you have any further questions, please reply to gen...@soe.ucsc.edu. All messages sent to that address are archived on a publicly-accessible Google Groups forum. If your question includes sensitive data, you may send it instead to genom...@soe.ucsc.edu.
Gerardo Perez
UCSC Genomics Institute
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