ALIGNING TWO FASTQ FILES OR TWO BAM-SORTED FILES
How to align two fastq(unpaired) files with each other before mapping or align reads at the level of indexing? Is there any working tool to do the job?
• 1,508 views
•
link
written
by
me.sr1510 •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
How to identify mitochondrial contamination in RNAseq and QC data?
written by mohammedtoufiq91
-
Comparing fastq files
written by diffexp123 •
-
Accurately identifying long non coding RNA from stranded total RNAseq(rRNA depleted)
written by m.sadman.sakib
-
merging multiple pair end read files into one
written by Bioinfonext
-
group reads by sequence length
written by genya35 •
-
tools to align DNA sequences against protein sequence
written by Ana
-
multiple Fastq file alignment
written by me.sr1510 •
-
Problem when having multiple Tophat runs inside one workflow in Galaxy
written by tunl
-
problem with newbler(error)
written by midox
-
Why Do We Align Each Pair Set Separately In An Illumina Paired End Sequencing Study?
written by Biomed
WHAT ARE YOU TRYING TO ACHIEVE AT THE END ?
and what is the difference with your previous question : multiple Fastq file alignment
Hello me.sr1510!
We believe that this post does not fit the main topic of this site.
Not a specific question, please describe your problem in detail and use google.
For this reason we have closed your question. This allows us to keep the site focused on the topics that the community can help with.
If you disagree please tell us why in a reply below, we'll be happy to talk about it.
Cheers!