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Hello Leinal: If you are mapping reads from a human whole genome sequencing experiment to the Chromosome 6 ONLY, then reads that might map to a (somewhat) similar genome sequence on another chromosome might be erroneously mapped to a region on Chr 6. Whole genome reads should always be mapped back to whole genome reference, and then you can use IGV to view the reads that map to your genome region of interest. Your alignment seems quite odd, but it is not a problem in IGV.. it is a problem during the read mapping step. If you have paired end reads, then definitely check the mapping / alignment of the paired read too. Cheers, Hugo
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--Gregory A. NewbyPost-doctoral fellowLaboratory of David LiuBroad Institute of MIT and Harvard75 Ames Street, Room 3010Cambridge, MA 02142
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--Gregory A. NewbyPost-doctoral fellowLaboratory of David LiuBroad Institute of MIT and Harvard
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--Gregory A. NewbyPost-doctoral fellowLaboratory of David LiuBroad Institute of MIT and Harvard
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--Gregory A. NewbyPost-doctoral fellowLaboratory of David LiuBroad Institute of MIT and Harvard75 Ames Street, Room 3010Cambridge, MA 02142
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