How can I convert output from Jim Kent's BLAT, which is in PSL format, into BED format?
Unconfigured Ad
Collapse
X
-
I have posted a new psl2bed conversion script to an unstable development branch of our BEDOPS suite, which you can download as follows:
$ svn checkout http://bedops.googlecode.com/svn/branches/v2p1p0 bedops_v2p1p0
$ cd bedops_v2p1p0
$ make
$ make install
$ cd bin
$ ./psl2bed --help
This script will convert headerless (default) and headered PSL files by moving columns around into BED output that follows UCSC BED format conventions, up to the first six columns. Remaining fields are mapped to columns 7 through 21.
Run psl2bed --help for a more complete description.
As an example, here is how to make a sorted BED file called sorted-foo.bed, converted from a headered PSL file called foo.psl:
$ psl2bed --headered < foo.psl > sorted-foo.bed
This relies on installing BEDOPS binaries, including psl2bed and sort-bed in a location accessible through your PATH environment variable.
Note that this is a development branch, so there are no guarantees that versions of BEDOPS apps made from this branch are stable. These and other improvements will end up in the final v2.1 release of BEDOPS, hopefully in a month or two.Last edited by AlexReynolds; 03-09-2013, 03:06 AM.
-
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
27 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
20 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
36 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
43 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
Comment