Locate genomic intervals using Interval Finder |
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When performing an HD probe search or SNP probe search, or creating probes using Genomic Tiling, you can enter a genomic interval as a parameter. To help you identify genomic intervals of interest, the Interval Finder can produce a list of genomic intervals that are associated with specific annotations.
Note: Interval Finder is not available in the Expression application type.
Click the Workspace tab. (Interval Finder searches are not available in collaborations.)
Click Probe
, then select Interval Finder.
The Interval Finder pane appears.
In Search Type, select one of the following options, then enter the desired search terms as described below.
Option |
Instructions/Details |
All |
This type of search returns intervals that have any annotation that matches a single search term that you enter.
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Accessions |
In Search Term(s), type an accession number, without its source, or multiple accession numbers separated by pipe "|" characters. The search returns the genomic intervals that correspond with each of the accessions. For the search to return intervals, accessions must match exactly. Use upper case (capital) letters in accessions. Example: NM_012257|Q0055|NM_012298 You can also upload a file of accessions. Prepare a plain text file with an extension of .txt. Put one accession on each line, and end each line with a new line character (press Enter). To upload the file, click Upload. For details, see Upload data for probe searches. |
Cytoband |
In Search Term(s), type a cytoband designation, without its source, or multiple cytobands separated by pipe "|" characters. The search returns the genomic intervals that correspond with each of the cytobands. For the search to return intervals, cytobands must match exactly. Use lower case letters to specify the p or q chromosome arms. Example: 1p22.2|2q33.3 You can also upload a file of cytobands. Prepare a plain text file with an extension of .txt. List one cytoband per line, and end each line with a new line character (press Enter). To upload the file, click Upload. For details, see Upload data for probe searches. |
Gene Symbol |
In Search Term(s), type a gene symbol, or multiple gene symbols separated by pipe "|" characters. The search returns the genomic intervals that correspond with each of the gene symbols. For the search to return intervals, gene symbols must match exactly. Use upper case (capital) letters in gene symbols. Example: H3N2|BRMS1|BRCA1 You can also upload a file of gene symbols. Prepare a plain text file with an extension of .txt. List one gene symbol per line, and end each line with a new line character (press Enter). To upload the file, click Upload. For details, see Upload data for probe searches. |
In Species, select the desired species. H. sapiens is selected by default.
Click Search.
eArray retrieves the genomic intervals. A Search Results pane appears.
For each interval, the pane shows the associated annotation, the genomic
coordinates of the interval, and a brief description.
After eArray displays the retrieved
genomic intervals, you can take action on them.
Use the tasks in the table below to navigate among the returned intervals and select them for further action.
Task |
Instructions/Details |
Select a single interval |
Mark the check box in its row. |
Select additional intervals |
Mark the check boxes next to the
name of each desired interval. |
Go to another page of Search Results |
Click the Pages links. eArray remembers your selections as you go from page to page. |
Sort the results |
Click the heading of a column. |
Select all intervals on all pages |
Mark Select Entire Result. |
Select all intervals on one page |
Mark the check box in the column heading row. |
Use the tasks in the table below to take action on the intervals that you selected in the previous step.
Task |
Instructions/Details |
Download the selected intervals as a list |
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Download the selected intervals as a BED format file |
This task can be useful if you want to use the selected intervals in a genome browser or other software that accepts BED format files.
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Start a new HD search based on the selected intervals |
(CGH and ChIP application types)
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Start a Genomic Tiling job based on the selected intervals |
(SureSelect Capture Array application type)
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Start a SNP probe search based on the selected intervals |
(CGH application type) Download the selected intervals, as described at the top of this table, then upload them in the Genomic Intervals parameter. See Search for SNP probes. |
Download a list of the search terms that did not return any intervals |
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View a list of the chromosomes associated with the selected intervals |
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See also