3b7a323713edb0adefb48de6a5fc81e8265e4067 gperez2 Sat Mar 28 11:22:26 2026 -0700 Adding a QuickLift documentation link to the Notes sectiono on hgConvert, refs #36111 diff --git src/hg/htdocs/goldenPath/help/hgConvert.html src/hg/htdocs/goldenPath/help/quickLift.html similarity index 96% rename from src/hg/htdocs/goldenPath/help/hgConvert.html rename to src/hg/htdocs/goldenPath/help/quickLift.html index 3a1fc2cef2e..12b8736cb60 100755 --- src/hg/htdocs/goldenPath/help/hgConvert.html +++ src/hg/htdocs/goldenPath/help/quickLift.html @@ -1,15 +1,24 @@ + + + + + + + +

QuickLift Help Page

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Overview

An alignment between two DNA sequences maps every nucleotide in one sequence to a nucleotide in another sequence. By making and using whole-genome alignments, the UCSC Genome Browser always allowed users to "lift" genome annotations to another assembly (liftOver), in bulk, one track at a time. QuickLift is a tool that uses the same algorithm, but it maps (liftOver) annotations on demand, in real-time, for all visible tracks. Only the annotations in the currently visible region are lifted, so this is usually fast enough when browsing a genome. For example, QuickLift can be used to map annotations from hg38 or hg19 to any of the hundreds of new human high-quality genomes in GenArk @@ -132,15 +141,17 @@ utility

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