Hi all,
This is probably a rather basic question but here it goes. Up until recently I have been doing RNA-seq using single-ended sequence reads....
5 results in 0.0036 seconds.
-
is bedtools paired-end aware?
-
Samtools MPILEUP on single-end/paired-end data
Hi everybody,
for variant calling, i am using samtools mpileup.
as far as i know, mpileup is by default ignoring certain... -
Can regular single end sequencing tell the transcription of genes in a strand-specifi
Just a very basic question (maybe too easy). Can regular single end sequencing tell the transcription of genes in a strand specific manner? -
Calling structural variants (CNVs) with single-end reads
Hi,
I would like to hear if anyone tried calling structural variants using single-end data. It seems that most of the tools available for... -
Sequencing/Capture problems
Has anyone experienced that the sequences generated after the capture are mostly those not included in the capture??
I have just looked at 1/10...
