bedtools | A powerful toolset
kandi X-RAY | bedtools Summary
kandi X-RAY | bedtools Summary
A powerful toolset for genome arithmetic.
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QUESTION
I am a very new beginner in bash programming and never succeed in installing tools on my computer.
I am trying to install bedtools without any success
I typed these following commands on my terminal
...ANSWER
Answered 2022-Mar-05 at 17:07It looks like you accidentally downloaded and compiled the program under your my_bin
directory. That creates some potential for confusion, so I would recommend running the wget
and make
commands from a temporary directory, such as /tmp
or a tmp
directory under your home directory. As a result, the compiled binaries are now under /Users/avitrac/my_bin/bedtools2/bin
. I would recommend moving that directory outside of your my_bin
directory, perhaps to a ~/tmp
directory; you could then skip directly to step 5 below.
(You could leave it there and simply cp /Users/avitrac/my_bin/bedtools2/bin/bedtools ~/my_bin
, but that would leave the source code and compilation artifacts under your bin directory for no good reason).
mkdir ~/tmp
## if neededcd ~/tmp
wget https://github.com/arq5x/bedtools2/releases/download/v2.29.1/bedtools-2.29.1.tar.gz
make
cp bin/bedtools ~/my_bin/
The bedtools-2.29.1.tar.gz
file and bedtools2
directory can both be removed now. The "Compiling from source via Github" instructions gloss over this (fairly typical) use-case and omitted the explicit instructions to build the program in a temporary location.
QUESTION
I have a very large file (~700M rows) and I would like to reduce the size by grouping mostly matching rows. Specifically, the file is sorted by fields 1 and 2 and I would like to group rows where field 2 contains consecutive numbers but all other fields match. If there is a gap in field 2 or if any other fields do not match the previous row then I would like to start a new interval. Ideally, I would like the output to return the interval range for the grouped rows and would prefer a solution that works in bash with awk and/or sed. I'm open to other solutions as well as long as they don't require re-sorting or other operations that might crash with such a long file.
The input file looks something like this.
...ANSWER
Answered 2021-Aug-03 at 21:53I doubt there is a standard tool like uniq -c
for this. But you can use this custom awk
script:
QUESTION
I'm doing an internship (= yes I'm a newbie). My supervisor gave told me to create a conda environment. She passed me a log file containing many packages.
A quick qwant.com search shows me how to create envs via the
...ANSWER
Answered 2021-May-06 at 15:41alright, so, it seems that they give you the output of conda list
rather than the .yml file produced by conda with conda env export > myenv.yml
. Therefore you have two solutions:
You ask for the proper file and then proceed to install the env with conda built-in pipeline
If you do not have any access on the proper file, you could do one of the following:
i) Parse with python into a proper .yml file and then do the conda procedure.
ii) Do a bash script, downloading the packages listed in the file she gave you.
This is how I would proceed, personally :)
QUESTION
to speed up a my workflow I would like to do something similar to snakemake-unknown-output-input-files-after-splitting-by-chromosome
...ANSWER
Answered 2021-Jan-15 at 08:08The Dynamic Files feature of Snakemake is probably what you need:
Dynamic files can be used whenever one has a rule for which the number of output files is unknown before the rule was executed.
You should wrap the "results/{sample}_{chrom}.bed"
with dynamic()
modifier in both input and output counterparts:
QUESTION
I would like to input a variable in the place of a file in the command below, is this possible?
I would like to generate some FASTA files using the programme bedtools getfasta
. Typically I would order the input files first using the awk
to bedtools sort
commands below. The output is then piped into an output file. This output file would then follow the -bed
flag in bedtools getfasta
so I can create the FASTA files I require, e.g.
ANSWER
Answered 2020-Dec-17 at 16:20If you look in the test suite for the bedtools getfasta
command, you'll see that it passes the word stdin
as a filename when it wants the BED input to be read from stdin. For example:
QUESTION
I am trying to extract fasta sequences from a genome using a bed file (homemade). The bed file looks like this (tab separated):
...ANSWER
Answered 2020-Jun-29 at 14:21According to bed format, the strand is on the 6th column, so in your example just move the strand to the 6th column:
QUESTION
I'm trying to learn how to code. I have to say that I'm using the Ubuntu app on the Windows system, so I don't know if my problems are related to this system. I established these variables in the terminal
...ANSWER
Answered 2020-Jul-01 at 16:16You need to export the variables so that they'll be inherited by the shell process running the script.
QUESTION
I have a data table in R which I want to count the number of overlapping windows for. This is essentially a pileup command and seems to be something that could be done using bedtools, but I can't figure out how to do so without leaving R.
Is there an R function to do this already, or any suggestions about what may be an efficient approach?
In case it's helpful, here is a mini example of what I'm trying to do. Thanks in advance!
input:
...ANSWER
Answered 2020-Jun-25 at 22:43You can use GenomicRanges, first we create the GRanges object:
QUESTION
I have two bedfiles as dataframes in R, for which I want to map all overlapping regions to each other (similar to what bedtools closest would be able to do).
BedA:
...ANSWER
Answered 2020-May-11 at 12:00Here is a solution using the data.table
package.
QUESTION
I would like to combine two command lines as one single to avoid the intermediate files.
...ANSWER
Answered 2020-Feb-19 at 09:42You probably get an invalid syntax because of the "
you use in your shell here: Description="Gene name">
. This closes your shell. You can either escape these quotes or use the """
syntax:
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