Is there a tool or script that can help identify false positives from a BAM file? Thanks.
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We use Ion Torrent PGM sequencing and use the aligned hg19 BAM in NextGene. I know that TVC is better at removing false positive variants, presumably because it has access to the SFF file and which contain signal values in flow space and a mapping between sequence. Is there a preferred or optimal way to asses MAPQ in the BMA alignment? Thanks.Last edited by cmccabe; 08-25-2014, 06:07 AM.
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I have contacted them and explained the issue. I am sure that future versions of the software will get better, but in the meantime I want to ensure that we are providing the best information possible. I am looking for some ideas from community members in developing a perl script to help address this. Some of the false positive calls have great PhreD scores (> 20), with good balance, so I am stumped. Thanks.
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