Below is the alignment of my paired-end reads from targeted sequencing. There are many soft clipped reads as shown from the highlighted region. What do they mean and what are the potential source of these clipped bases? (Reads have been removed for adapter using fastp software). Thanks
What is difference between soft-clipped and hard-clipped in SAM specification?
Here is a nice post regarding the effect of soft cliping: https://sequencing.qcfail.com/articles/soft-clipping-of-reads-may-add-potentially-unwanted-alignments-to-repetitive-regions/
And here in depth explanation: https://davetang.org/wiki/tiki-index.php?page=SAM