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On this page you find all important commands for the CLI tool bedtools. If the command you are looking for is missing please ask our AI.

bedtools

Bedtools is a powerful and widely used command line tool for genomic analysis. It is specifically designed to manipulate and analyze genomic intervals, typically represented in the BED format.

Some key features of bedtools include:

  1. Interval operations: Bedtools provides a wide range of operations for intersecting, merging, subtracting, and comparing intervals. These operations enable users to perform tasks such as finding overlapping regions, identifying unique intervals, and locating gaps between intervals.

  2. Genomic arithmetic: Bedtools allows users to perform mathematical operations on intervals, such as scaling, shifting, and calculating the union or intersection of intervals. This is particularly useful for tasks like scaling interval coordinates or finding the overlap of intervals across different samples or datasets.

  3. File format conversions: Bedtools supports seamless conversion between various genomic file formats, including BED, GFF, VCF, SAM, BAM, and more. This flexibility makes it easy to integrate bedtools into existing analysis pipelines or work with different file formats.

  4. Fast and memory-efficient: Bedtools is optimized for performance and handles large datasets efficiently, making it suitable for working with genome-scale data. It employs advanced indexing strategies to rapidly access specific regions of interest, reducing computational time and memory requirements.

  5. Extensible and scriptable: Bedtools provides a comprehensive set of command line options that can be combined in complex ways to create custom analysis pipelines. It is also compatible with other bioinformatics tools and scripting languages, enabling users to automate their genomic analyses.

Overall, bedtools is a versatile and indispensable tool for genomic research, enabling researchers to efficiently manipulate and analyze interval data. It has gained widespread usage in the genomics community and remains an essential component of bioinformatics workflows.

List of commands for bedtools:

  • bedtools:tldr:02091 bedtools: Convert bam-formatted file to a bed-formatted one.
    $ bedtools bamtobed -i ${filename}.bam > ${filename}.bed
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  • bedtools:tldr:7347d bedtools: Find for all features in {{file_1}}.bed the closest one in {{file_2}}.bed and write their distance in an extra column (input files must be sorted).
    $ bedtools closest -a ${filename_1}.bed -b ${filename_2}.bed -d
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  • bedtools:tldr:77d8f bedtools: Intersect two files with a left outer join, i.e. report each feature from {{file_1}} and NULL if no overlap with {{file_2}}.
    $ bedtools intersect -a ${filename_1} -b ${filename_2} -lof > ${path-to-output_file}
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  • bedtools:tldr:8b38f bedtools: Intersect two files regarding the sequences' strand and save the result to the specified file.
    $ bedtools intersect -a ${filename_1} -b ${filename_2} -s > ${path-to-output_file}
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  • bedtools:tldr:b6f90 bedtools: Group file {{`path/to/file`}} based on the first three and the fifth column and summarize the sixth column by summing it up.
    $ bedtools groupby -i ${filename} -c 1-3,5 -g 6 -o sum
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  • bedtools:tldr:f5eee bedtools: Using more efficient algorithm to intersect two pre-sorted files.
    $ bedtools intersect -a ${filename_1} -b ${filename_2} -sorted > ${path-to-output_file}
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tool overview