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The multi-region display allows users to "slice" their track viewing experience into a
variety of different modes that focus the display on certain features: exon-only, gene-only, or
user-defined BED coordinates. Only the portions of track annotations that fall within these
displayed regions are shown; extraneous intergenic, intronic and otherwise unwanted regions are
hidden from view.
For human assemblies hg17 and later, the multi-region view also supports the replacement of a
section of the reference genome with an alternate haplotype chromosome. This allows the user to view
annotations upstream and downstream of the haplotype sequence, and visualize the haplotype in the
general context of the reference chromosome.
Using the multi-region display, one can:
Show all SNPs that fall within exons (exon-only view).
Show only the genes on a chromosome (gene-only view).
Display the same chromosomal position on either side of a gene in order to model a repeat region
(using custom regions in BED format).
See how an alternate haplotype fits onto its chromosome (alternate haplotype view).
Getting started With Multi-Region view
Follow these steps to activate and configure multi-region view in the Genome Browser.
Step 1. Pick a genome assembly and region
Open the Genome Browser tracks display to a region of interest within a standard genome assembly, or
open a custom region within an assembly hub.
Step 2. Open the multi-region view configuration window
Click under the tracks display to open the multi-region
configuration window.
Step 3. Configure the multi-region view
By default, the Exit multi-region mode button is selected. This button returns the
display to the traditional view.
To activate a multi-region view, click one of these options:
Show exons using -- display only the exonic regions (keyboard shortcut:
"e v")
Show genes using -- display only those regions with gene annotations in the
specified genes track
Enter custom regions as BED, or a URL to them -- display only those regions entered into the
text box in BED format, or listed in a specified BED file
Show one alternate haplotype -- display the specified alternate haplotype in
place on the reference chromosome (human assemblies hg17 and later only)
(Optional) Select Highlight alternating regions in multi-region view to color
alternating slices in blue.
Click to save your changes and return to the Genome Browser tracks display.
Here is a view of the Genome Browser with the "Show exons" and "Highlight alternating
regions" options selected:
Navigation and display
With a few exceptions, most browser navigation and display features function the same in both
multi-region and single-chromosome modes, including zooming in and out, reversing and resizing the
view, highlighting and zooming to a selected region, and track search. Searching and zooming
conventions differ when displaying custom BED regions. See About Custom
Regions for more information.
About the Multi-Region modes
Exon-only mode
The exon-only view shows only those bases and annotations that fall within an exon or padding
region. Bases and alignments within intronic and intergenic regions are removed from the
display.
The exon-only view "virtual chromosome" is constructed of all the exons present in the
gene track specified in the multi-region configuration window. Exon "slices" are visually
separated by blocks of intronic or intergenic bases, the size of which are set by the padding field.
This designates the padding on both sides of an exon, and therefore is additive, e.g., a padding
size of 6 will result in a 12-base space between exon slices:
If the gene track used to compute the slicing is a
super track or contains other transcripts, only
the longest exon will be used to determine slicing, regardless of whether or not they are in the same transcript. See Example 1 for more information.
Gene-only mode
The gene-only view displays the bases and annotations that fall within the coordinates of a gene,
but hides all of the intergenic bases except those used for padding
(Example 2). As with exon-only mode, the padding field sets the number of
intergenic bases displayed to visually separate each gene slice.
Because genes and alternate transcripts often overlap by a few bases, the windows created by the
gene-only (and exon-only) mode may sometimes merge together. Reducing the number of padding bases
may increase the number of alternate regions by allowing less intergenic space between genes.
However, this overlap is a common feature for most of the Genome Browser gene sets, and should be
no cause for concern.
Custom regions mode
The custom regions mode allows user-specific modeling of genomic regions by either entering them into the
text box, or linking to a
BED file. Typically when a BED file is loaded into
the browser, the entries are displayed in the tracks window in order of chromosomal location,
regardless of the order in the file. When the multi-region view option is selected, the BED file
entries are displayed in the same order they appear in the file. This feature can be used to
manipulate the display of other annotations in the browser window, for example to duplicate a
display region, reorder the exon display within a gene, or display regions from 2 different
chromosomes side-by-side. Example 3 demonstrates the importance of ordering
entries within a file.
Although all types of BED files are supported, only the information from BED 3 or BED 12 files is
relevant to the display. Like BED custom tracks, comments are supported in the BED files used by
multi-region mode. Comments are included at the top of the BED file, preceded by "#". The
supported comments are:
#database: The genome assembly database for which the BED file is intended. If
the file is loaded onto a different assembly, the custom regions mode will not work.
#shortDesc: (Optional) A short description of the custom region, displayed next
to the chromosome ideogram.
#padding: Sets the size of the padding on either side of a BED entry in the
browser tracks window.
Here is an example of a BED3 file with comments:
#database hg38
#shortDesc Example of a short description
#padding 6
chr1 pos1 pos2
chr2 pos1 pos2
The Genome Browser search mechanism functions differently when using custom BED regions in
multi-region view. When searching for a term or position, the browser first searches for the term
within the BED-defined regions. If the item is found, the browser display will shift to that
location.
If the term is not found within the BED-defined regions, but is found elsewhere, the browser
will display a message asking if you would like to return to a default view at that
location. If you prefer to return to your custom region instead, click
. Otherwise, click "here" to return to the default
view.
If the term is not found at all in the assembly, an error message will display.
When scrolling or zooming while viewing regions from a custom BED URL, the range is restricted to
the BED-defined regions. Although you can still zoom in to single base resolution, the outward zoom
is limited to the extent of the defined regions. Scrolling upstream and downstream is also limited
to the BED-defined range.
Haplotype mode
An additional viewing mode is available on human assemblies hg17 and later: showing an alternative
haplotype placed in its chromosomal context (Example 5). The haplotype is
specified by entering its ID in the form chr_name_alt in the configuration window. To view
the list of haplotype IDs for a given assembly, go to
http://hgdownload.soe.ucsc.edu/goldenPath/$db/bigZips/$db.chrom.sizes,
where $db is the human assembly name (e.g., hg38, hg19, hg18 or
hg17).
Alternatively, haplotypes can be viewed using the Alt Map... track in the Mapping
and Sequencing group. Open the track and navigate to the haplotype of interest in the track window.
Click on the haplotype to display its details page, then click the link Show this alternate
haplotype placed on its chromosome.
Examples
Example 1. Exon-only mode
This screenshot shows the exon-only view for the SOD1 gene in human assembly hg38. The third
"exon" from the left falls within the intron of the actual SOD1 gene, but is shown as an
exon because it is part of the GENCODE v22 super-track.
Click here
to view this example in the Genome Browser. To quickly exit multi-region mode and return to
the default single chromosome view, use the keyboard shortcut "d v".
Example 2. Gene-only mode
This example illustrates how intergenic regions are removed from the default browser tracks view in
gene-only mode. The displayed region of the X chromosome on the human hg19 assembly consists of
three genes (DKC1, MPP1, and F8) with varying amounts of intergenic space separating them. The first
screenshot shows the standard browser display of the gene track in "single chromosome"
view. Compare it with the second screenshot, which shows the same region in gene-only mode with the
padding set to 6. (Click
here
to view this example in the Genome Browser.)
To quickly exit multi-region mode and return to the default single chromosome view, use the
keyboard shortcut "d v".
Example 3. Custom regions from BED file
Here is an example BED file for mm10 that
contains a list of exon positions for the Pax9 gene. If this file is loaded into the browser as a
custom track without turning on multi-region mode, the blocks display in order of genomic
position, not in the order they are specified in the file:
However, if multi-region mode is turned on after loading a custom track, the blocks display in the
order they are listed in the BED file, rather than in genomic position order. This in turn affects
the display order of other features in this view, in this case the display order of the exons in
Pax9. This feature can be used to manipulate the display of other annotations, for example to allow
the visualization of centromeric regions or viewing the same gene twice within the same window to
compare annotations in a separate region.
Click
here
to view this example in the Genome Browser. To quickly exit multi-region mode and return to the
default single chromosome view, use the keyboard shortcut "d v".
Example 4. BED12
The following BED file utilizes BED12 format
to display two regions from two different chromosomes, chromosome 22 and chromosome 21, side-by-side
in the browser tracks window, along with human genes POTEH, CECR2, USP25 and CHODL.
The multi-region display utilizes the data in the blockStarts and blockSizes fields of the BED file
to draw its regions, allowing for even more customization of the Genome Browser display.
Click
here
to view this example in the Genome Browser. To quickly exit multi-region mode and return to the
default single chromosome view, use the keyboard shortcut "d v".
Example 5. Haplotype
This example shows how the human hg38 haplotype chr1_KI270762v1_alt fits onto chromosome 1. Note
that annotations from the standard browser display do not extend into or out of the haplotype
region, since haplotypes are annotated separately from regular chromosomes.
Click
here
to view this example in the Genome Browser. To quickly exit multi-region mode and return to the
default single chromosome view, use the keyboard shortcut "d v".
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