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14 | 14 | ##INFO=<ID=LSEQ,Number=1,Type=String,Description="5' flanking seq"> |
15 | 15 | ##INFO=<ID=RSEQ,Number=1,Type=String,Description="3' flanking seq"> |
16 | 16 | ##INFO=<ID=STATUS,Number=1,Type=String,Description="Somatic or germline status"> |
| 17 | +##INFO=<ID=P0.01Likely,Number=0,Type=Flag,Description="Likely candidate but p-value > 0.01/5**vd2 (means the evidence in tumor sample might be weak, e.g. small diff in AF)"> |
| 18 | +##INFO=<ID=IndelLikely,Number=0,Type=Flag,Description="Likely indels more than 2bp are not considered somatic (weak evidence of presence in normal samples)"> |
17 | 19 | ##FILTER=<ID=q22.5,Description="Mean Base Quality Below 22.5"> |
18 | 20 | ##FILTER=<ID=Q0,Description="Mean Mapping Quality Below 0"> |
19 | 21 | ##FILTER=<ID=p8,Description="Mean Position in Reads Less than 8"> |
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26 | 28 | ##FILTER=<ID=f0.02,Description="Allele frequency < 0.02"> |
27 | 29 | ##FILTER=<ID=P0.05,Description="Not significant with p-value > 0.05"> |
28 | 30 | ##FILTER=<ID=DIFF0.2,Description="Non-somatic or LOH and allele frequency difference < 0.2"> |
29 | | -##FILTER=<ID=P0.01Likely,Description="Likely candidate but p-value > 0.01/5**vd2"> |
30 | | -##FILTER=<ID=InDelLikely,Description="Likely Indels are not considered somatic"> |
31 | 31 | ##FILTER=<ID=MSI12,Description="Variant in MSI region with 12 non-monomer MSI or 12 monomer MSI"> |
32 | 32 | ##FILTER=<ID=NM5.25,Description="Mean mismatches in reads >= 5.25, thus likely false positive"> |
33 | 33 | ##FILTER=<ID=InGap,Description="The somatic variant is in the deletion gap, thus likely false positive"> |
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