What are chimeric reads? Is there any effective method to distinguish chimeric reads from normal ones? Can someone point me to a survey or reviews on that topic? Thank you a lot!
Zhen
What are chimeric reads? Is there any effective method to distinguish chimeric reads from normal ones? Can someone point me to a survey or reviews on that topic? Thank you a lot!
Zhen
Chimeric reads occur when one sequencing read aligns to two distinct portions of the genome with little or no overlap. Chimeric reads are indicative of structural variation. Chimeric reads are also called split reads.
After aligning with bwa mem, chimeric reads will have an SA tag as described on page 7 of the SAM format specification. To find them all you have to do is extract them using grep.
samtools view my_alignment.bam | grep 'SA:' | less
For reference:
Chimerism condition in which a gene is formed from combination of two other genes. Suppose part of your gene is matching to one gene ( also of species) and other part is matching to other gene (also can be from different species).
If you want to detect chimerism in your sequence, the simplest way is to match your gene to NCBI or any other database. Then check the alignment hits. If there chimerism exists, part of your gene will match to different genes.
A simple explanation: http://drive5.com/usearch/manual/chimera_formation.html
possibly here now https://drive5.com/usearch/manual/chimeras.html
Chimeric reads is the sequence form through the combination of portions of one or more coding sequences to produce new genes.
http://scienceblogs.com/digitalbio/2007/02/01/sequencing-a-genome-part-vi-ch/
Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Linear alignment
vschimeric reads
chimeric reads
vssoft clipping
vshard clipping
representative
vssupplementary
alignmentMultiple mapping
Is there a way of forcing a linear alignment with bwa?
This might be relevant: http://scienceblogs.com/digitalbio/2007/02/01/sequencing-a-genome-part-vi-ch/