Dear all,
I'm analyzing small RNA seq data.
I have the genomic coordinates of some elements (called cluster) on the genome.
I have to make some graph, representing the density of small RNA mapping to these cluster using a windows size of 250nt and step size of 25 nt ( i have to do this because it has already been done in a paper).
I'm not sure to well understand :
does it mean that i have to created a BED file called windows.bed for 250nt windows across the element of interest and that each windows overlap by 25 nt.
For example :
and i create a 2nd bed file of sequence reads called reads.bed
And i can use coverageBed from Bedtools to calculate for each window in windows.bed the number of reads in reads.bed that overlap the window.
Do i well understand the notion of window size / step size ?
Thanks in advance for your help,
Stéph
and then, i can use Bedtools
I'm analyzing small RNA seq data.
I have the genomic coordinates of some elements (called cluster) on the genome.
I have to make some graph, representing the density of small RNA mapping to these cluster using a windows size of 250nt and step size of 25 nt ( i have to do this because it has already been done in a paper).
I'm not sure to well understand :
does it mean that i have to created a BED file called windows.bed for 250nt windows across the element of interest and that each windows overlap by 25 nt.
For example :
Code:
chr1 0 250 chr1 225 475 ....
And i can use coverageBed from Bedtools to calculate for each window in windows.bed the number of reads in reads.bed that overlap the window.
Do i well understand the notion of window size / step size ?
Thanks in advance for your help,
Stéph
and then, i can use Bedtools
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