Hello
when I try to run rm on multiple files I have problem to delete files with space.
I have this command :
find . -name "*.cmd" | xargs \rm -f
it doing the work fine but when it comes across files with spaces like : "my foo file.cmd"
it refuse to delete it
why? (1 Reply)
Question for anyone that might be able to help:
My objective is to eheck if a file (a source file) exists in a directory. If it does then, I'd like to call an application (Informatica ETL file...not necessary to know) to run a program which extracts data and loads it into multiple targets.
... (6 Replies)
Hi,
I have thousands of files in a directory that have the following 2 formats:
289620178.aln
289620179.aln
289620180.aln
289620183.aln
289620184.aln
289620185.aln
289620186.aln
289620187.aln
289620188.aln
289620189.aln
289620190.aln
289620192.aln....
and:
alnCDS_1.fasta (1 Reply)
Hi,
I want to run a Perl script on multiple files, with same name ("Data.txt") but in different directories (eg : 2010_06_09_A/Data.txt, 2010_06_09_B/Data.txt).
I know how to run this perl script on files in the same directory like:
for $i in *.txt
do
perl myscript.pl $i > $i.new... (8 Replies)
Hi
I have 1000 files labelled data1.txt through data1000.txt. I want to write a script that prints out the number of lines in each txt file and outputs it in the following format:
Column 1: number of data file (1 through 1000)
Column 2: number of lines in the text file
Thanks! (2 Replies)
Hi everyone,
I'm new to the forums, as you can probably tell... I'm also pretty new to scripting and writing any type of code.
I needed to know exactly how I can grep for multiple strings, in files located in one directory, but I need each string to output to a separate file.
So I'd... (19 Replies)
Hi
I have 100 files under file A labled 1.txt 2.txt.....100.txt(made up name)
I have 1 files under file B labled name.txt
How can i run the same perl script on 100 files and file name.txt
I want to run
perl script.pl A/1.txt B/name.txt
perl script.pl A/2.txt B/name.txt
.......
perl... (3 Replies)
How can I run the following command on multiple files and print out the corresponding multiple files.
perl script.pl genome.gff 1.txt > 1.gff
However, there are multiples files of 1.txt, from 1----100.txt
Thank you so much.
No duplicate posting! Continue here. (0 Replies)
I have a script that I need to run on one file at a time. Unfortunately using for i in F* or cat F* is not possible. When I run the script using that, it jumbles the files and they are out of order. Here is the script:
gawk '{count++; keyword = $1}
END {
for (k in count)
{if (count == 2)... (18 Replies)
Hi Guys,
I've been having a look around to try and understand how i can do the below however havent come across anything that will work.
Basically I have a parser script that I need to run across all files in a certain directory, I can do this one my by one on comand line however I... (1 Reply)
Discussion started by: mutley2202
1 Replies
LEARN ABOUT DEBIAN
bio::graphics::glyph::vista_plot
Bio::Graphics::Glyph::vista_plot(3pm) User Contributed Perl Documentation Bio::Graphics::Glyph::vista_plot(3pm)NAME
Bio::Graphics::Glyph::vista_plot - The "vista_plot" glyph
SYNOPSIS
See Bio::Graphics::Glyph, Bio::Graphics::Glyph::wiggle_xyplot and Bio::Graphics::Glyph::heat_map.
DESCRIPTION
This glyph draws peak calls (features with discreet boundaries, i.e. putative transcription sites, over signal graph (wiggle_xyplot)
requires a special load gff file that uses attributes 'wigfile' and 'peak_type'
Example:
2L chip_seq vista 5407 23011573 . . . Name=ChipSeq Exp 1;wigfile=SomeWigFile.wigdb;peak_type=binding_site:exp1
The glyph will draw the wiggle file first, than overlay the peaks (if there are any) over signal graph. Elsewhere in the GFF3 file, there
should be one or more features of type "binding_site:exp1", e.g.:
2L exp1 binding_site 91934 92005 . . .
Options like 'balloon hover' and 'link' are available to customize interaction with peaks in detail view.
BigWig support:
Supported bigwig format also requires another attribute to be supplied in load gff file (fasta) which specifies sequence index file for the
organism in use. The data file should have the 'bw' extension - it is used to detect the BigWig format by vista_plot
3L chip_seq vista 1 24543530 . . . Name=ChipSeq Exp
2;wigfile=SomeBigWigFile.bw;peak_type=binding_site:exp2;fasta=YourOrganism.fasta
Note that all attributes should be present in load gff, as the code currently does not handle situation when only some of the attributes
are in gff. To omit peak or signal drawing use "" (i.e. peak_type="") In both cases, the stanza code will look the same (only essential
parameters shown):
[VISTA_PLOT]
feature = vista:chip_seq
glyph = vista_plot
label = 1
smoothing = mean
smoothing_window = 10
bump density = 250
autoscale = local
variance_band = 1
max_peak = 255
min_peak = 1
peakwidth = 3
start_color = lightgray
end_color = black
pos_color = blue
neg_color = orange
bgcolor = orange
alpha = 80
fgcolor = black
database = database_with_load_gff_data
box_subparts = 1
bicolor_pivot = min
key = VISTA plot
OPTIONS
Options are the same as for wiggle_xyplot and heat_map
Additional parameters:
alpha set transparency for peak area.
glyph_subtype Display only 'peaks', 'signal', 'density' or 'peaks+signal'. Aliases for 'peaks+signal' include "both" and "vista".
Recommended global settings:
for proper peak drawing transparency should be enabled by setting truecolors=1 in GBrowse.conf file
BUGS
Please report them.
SEE ALSO
Bio::Graphics::Panel Bio::Graphics::Glyph Bio::Graphics::Glyph::wiggle_xyplot Bio::Graphics::Glyph::heat_map GD
AUTHOR
Peter Ruzanov pruzanov@oicr.on.ca
Copyright (c) 2010 Ontario Institute for Cancer Research
This package and its accompanying libraries is free software; you can
redistribute it and/or modify it under the terms of the GPL (either
version 1, or at your option, any later version) or the Artistic
License 2.0. Refer to LICENSE for the full license text. In addition,
please see DISCLAIMER.txt for disclaimers of warranty.
perl v5.14.2 2012-02-20 Bio::Graphics::Glyph::vista_plot(3pm)