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To Calculate The Exact Total Number Of Mapped Reads In Exome Regions

Dear All, I have some questions here. I want to do some quality control analysis on my exome data that are mapped on the reference genome. I am having the input bam file for a sample which contains...

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Calculating Exome Coverage

*// Edit to make the post more clear (Mapping done via Bowtie2). My problem is that when counting Exome Coverage via coverageBed gives different results than via genomeCoverageBed. So I'm not sure if...

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Genbank to bed conversion for bedtools analysis

Hi, I need to use bedtools to obtain the coverage across two bam files for comparison. However, to do this, I need a .bed file of the genome features (of the reference genome used to generate the...

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Does Bedops Have A Command Similar To The Bedtools Makewindows?

With bedtools you can make genomic windows from a genome file or a bed fileinput.bedchr1 1000000 1500000 chr3 500000 900000[prompt]$ bedtools makewindows -b input.bed -w 250000chr1 1000000 1250000 chr1...

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Intersectbed: Return Reads In Fraction In Input Files

I have a question with respect to intersectBED and multiple input files:Is it possible to return reads which are present in, say 8/10 input files, without fractioning the reads in smaller...

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Identify Overlapping And Non Overlapping Regions For Paired-End Data

gene1 gene2 chr1 25 30 chr1 34 37 chr1 15 20 chr1 25 28 chr1 80 90 chr1 10 13 gene1 gene2 chr1 25 30 chr1 36 39 chr1 15 20 chr1 18 20 chr1 80 90 chr1 19 22 common gene1 uniq gene2 (when we compare file...

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Coveragebed, Depth/Breadth Of Coverage

I'm using coverageBed to calculate the depth and breadth of coverage, but I'm not sure I'm doing this right. I want to calculate the two values for each human chromosome. For example, I've created a...

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Tutorial: Introduction to bedtools.

We have created a basic tutorial introducing bedtools. It is intended for folks that are new to the tools, but in addition, there are some puzzles at the end that may be useful for people that use...

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How To Use Bedtools Windows To Overlap Upstream For Positive Strand Strand

Hi,I am trying to use bedtools windows. It has been explained in the manual of the bedtools but I am still bit confused and thought a confirmation would be good. And I have no biological background.I...

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Does Windowbed Extend Reads?

I am using WindowBed, part of the BedTools suite, to align reads to a reference file and I obtained a very interesting result. I am trying to rule out an analysis artifact that could be caused by...

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Bedtools Genomecoveragebed Usage : How To Create A Genome File?

I am using BEDTOOLS and the following command to get the coverage file:$ ./genomeCoverageBed -ibam ~/GG_project/trim/ecoli.bam -g > ~/GG_project/trim/coveragewhere ecoli.bam is my sorted bam file,...

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Correlation Of Fpkm And Length Normalized Transcript Mapped Read Count

Hello, in the process of estimating expression for a 16 human tissue dataset ("Human Body Map 2.0 GSE30611") I used different methods to estimate the expression of the genes. After mapping against hg19...

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Bedtools on Cygwin problem.

Hi   I'm trying to install the latest release of Bedtools via Cygwin but there's a weird error during process. I know this isn't the best solution, but I do not have an other choice. Perhaps anyone...

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How To Use Bedtools To Extract Promoters From A Mouse Bed File

Hello, I would like to know how to use Bedtools to extract promoter sequences (as FASTAs) from the mouse genome (mm9) starting from a BED file.

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How To Find The Nearest Gene To A Retrotransposon Insert?

Hi,I have a BED file with the position of retrotransposons in the mouse genome and I would like to find the nearest gene, the distance to that gene and whether it is on the + or - strand. There are so...

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Bed_intersect -s empty output

Hi!, I have problems with bedintersect. I need to intersect two bed files like these: A.bed   chr1    10568    10571    -    5 chr1    10568    10571    -    5 chr1    10568    10571    -    5 chr1...

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What Is The Best Way To Run Bedtools In Parallel With Blocking

Say I am working on a server with a shared file system and 4 quad core nodes (I/O is not an issue, 16 cores total). I want to run coverageBed across 20 files. Currently I have a shell script that would...

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Creating Bed File For Lncrna Using Gencode Gtf File

Hi all,I want to get the bed file of lncRNA based on GENCODE GTF fileI download the file "gencode.v16.long_noncoding_RNAs.gtf.gz", and extract the chr, start, end info from the file, then I use...

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Annotating Genomic Intervals

How can I annotate human genomic intervals (BED file) from a ChIP-seq experiment with information such as whether the interval overlaps with a gene(s)? Upstream of a gene? Overlaps with an exon?...

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bedtools 2.0 merge - "unable to open file or unable to determine types"

I have a sorted bedfile comprised of three columns: seqid, start, and end. sort -k1,1 -k2,2n tmp2.bed > tmp3.bed 1    6589256    6589207 1    11627195    12127194 1    12616616    12116617 1...

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