Does anyone know a program which can split BED file according to the chromosome? I have generate a BED file which contains the data for all chromosome, but it is not sorted. When I did sorting using BedSort, the output was not ordered according the numeric order, it always give chr10 on the top and then followed chr11, up to chr19. It seems I have to do the sorting for each chr respectively, I wonder whether there is a program which can split BED file according to the chromosome. Thanks
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You could try the following with your bed file:
if you want to split your bed file you could do with bash:Code:sort -k 1V,1 -k 2n,2 file.bed -o file.sorted.bed
Code:mkdir -p split_results for chr in `cut -f 1 file.bed | sort | uniq`; do grep -w $chr file.bed > split_results/$chr.output.bed done
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Similar to adamdeluca's suggestion, here is another simple awk solution. Note that the ">>" creates and appends to files named CHROM.bed, where CHROM is column 1 of the bed input bed file (in this case, example.bed).
So, in plain English, the awk command prints each entire line ($0) from example.bed to distinct files that are each named by the chrom field ($1).
This strategy is useful in many other cases where you want to do a context-based "grep", and route the results to distinct files.
arqCode:$ awk '{print $0 >> $1".bed"}' example.bed $ ls -1 *.bed chr1.bed chr2.bed ... (snip) chrY.bed example.bed
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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by SEQadmin2
I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
Here are nine questions we think about, in roughly the order they matter, before...-
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