I have sam files for the chimeric reads, which come from two different parts of the genome (For example, the first half of the read from part of Chromosome 1 and the second half of the read from part of Chromosome 3). I found 3 reads with the same ID in the sam files. Could anyone explain this? Thanks!
L180:234:HTHGMADXX:1:1101:1137:6179 99 V 10092485 60 29S33M = 10092488 63 ACATGTGCGAAAAAAAAACTTTGAGTATTTTGTGCGTTGATGATGTTGGGGGAATGAGTGTG BBBFFFFFFFFFFIIIIIFFFIFIFFFIFBFFFFIIBFFIIFIIIBFFFFFFBFFFFFBB<B NM:i:0 MD:Z:33 MC:Z:60M AS:i:33 XS:i:0 SA:Z:V,10092453,-,29S33M,60,0;
L180:234:HTHGMADXX:1:1101:1137:6179 2163 V 10092453 60 29H33M = 10092488 63 ACAAAATACTCAAAGTTTTTTTTTCGCACATGT FFFBFIFFFIFIFFFIIIIIFFFFFFFFFFBBB NM:i:0 MD:Z:33 MC:Z:60M AS:i:33XS:i:0 SA:Z:V,10092485,+,29S33M,60,0;
L180:234:HTHGMADXX:1:1101:1137:6179 147 V 10092488 60 60M = 10092485 -63 TGCGTTGATGATGTTGGGGGAATGAGTGTGACGAAATTGAAAAACTAAAAGCAGAAGTAG IIFIIIIIIIIFFIIIIIIIIIIIIIIIIFFIIIIIIIIIIIIFIFIFFFFFFFFFFBBB NM:i:0 MD:Z:60 MC:Z:29S33M AS:i:60 XS:i:0
could they just be multimapping?