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
Unconfigured Ad
Collapse
X
-
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
-
-
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
Comment
-
Latest Articles
Collapse
-
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...-
Channel: Articles
Yesterday, 07:11 AM -
-
by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
...-
Channel: Articles
06-02-2026, 10:05 AM -
-
by SEQadmin2
With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...-
Channel: Articles
05-22-2026, 06:42 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Whole-Genome Sequencing Traces Faroe Islands Ancestry to a North Atlantic Founder Population
by SEQadmin2
Started by SEQadmin2, 06-17-2026, 06:09 AM
|
0 responses
20 views
0 reactions
|
Last Post
by SEQadmin2
06-17-2026, 06:09 AM
|
||
|
Sequencing the Two-Toed Sloth Genome Reveals Jumping Genes Tied to Its Extreme Metabolism
by SEQadmin2
Started by SEQadmin2, 06-09-2026, 11:58 AM
|
0 responses
38 views
0 reactions
|
Last Post
by SEQadmin2
06-09-2026, 11:58 AM
|
||
|
Started by SEQadmin2, 06-05-2026, 10:09 AM
|
0 responses
45 views
0 reactions
|
Last Post
by SEQadmin2
06-05-2026, 10:09 AM
|
||
|
Started by SEQadmin2, 06-04-2026, 08:59 AM
|
0 responses
49 views
0 reactions
|
Last Post
by SEQadmin2
06-04-2026, 08:59 AM
|
Comment