Mercurial > repos > mini > strelka
comparison strelka_config.sample @ 6:87568e5a7d4f
Testing strelka version 0.0.1
author | mini |
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date | Fri, 26 Sep 2014 13:24:13 +0200 |
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5:07cbbd662111 | 6:87568e5a7d4f |
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2 ; | |
3 ; User configuration options for Strelka somatic small-variant caller | |
4 ; workflow: | |
5 ; | |
6 | |
7 [user] | |
8 | |
9 ; | |
10 ; isSkipDepthFilters should be set to 1 to skip depth filtration for | |
11 ; whole exome or other targeted sequencing data | |
12 ; | |
13 isSkipDepthFilters = 1 | |
14 | |
15 ; | |
16 ; strelka will not accept input reads above this depth (they will be skipped | |
17 ; until the depth drops below this value). Set this value <= 0 to disable | |
18 ; this feature. Using this filter will bound memory usage given extremely high | |
19 ; depth input, but may be problematic in high-depth targeted sequencing | |
20 ; applications. | |
21 ; | |
22 maxInputDepth = 10000 | |
23 | |
24 ; | |
25 ; If the depth filter is not skipped, all variants which occur at a | |
26 ; depth greater than depthFilterMultiple*chromosome mean depth will be | |
27 ; filtered out. | |
28 ; | |
29 depthFilterMultiple = 3.0 | |
30 | |
31 ; | |
32 ; Somatic SNV calls are filtered at sites where greater than this | |
33 ; fraction of basecalls have been removed by the mismatch density | |
34 ; filter in either sample. | |
35 ; | |
36 snvMaxFilteredBasecallFrac = 0.4 | |
37 | |
38 ; | |
39 ; Somatic SNV calls are filtered at sites where greater than this | |
40 ; fraction of overlapping reads contain deletions which span the SNV | |
41 ; call site. | |
42 ; | |
43 snvMaxSpanningDeletionFrac = 0.75 | |
44 | |
45 ; | |
46 ; Somatic indel calls are filtered if they represent an expansion or | |
47 ; contraction of a repeated pattern with a repeat count greater than | |
48 ; indelMaxRefRepeat in the reference (ie. if indelMaxRefRepeat is 8, | |
49 ; then the indel is filtered when it is an expansion/contraction of a | |
50 ; homopolymer longer than 8 bases, a dinucleotide repeat longer than | |
51 ; 16 bases, etc.) | |
52 ; | |
53 indelMaxRefRepeat = 8 | |
54 | |
55 ; | |
56 ; Somatic indel calls are filtered if greater than this fraction of | |
57 ; basecalls in a window extending 50 bases to each side of an indel's | |
58 ; call position have been removed by the mismatch density filter. | |
59 ; | |
60 indelMaxWindowFilteredBasecallFrac = 0.3 | |
61 | |
62 ; | |
63 ; Somatic indels are filtered if they overlap ’interrupted | |
64 ; homopolymers’ greater than this length. The term 'interrupted | |
65 ; homopolymer' is used to indicate the longest homopolymer which can | |
66 ; be found intersecting or adjacent to the called indel when a single | |
67 ; non-homopolymer base is allowed. | |
68 ; | |
69 indelMaxIntHpolLength = 14 | |
70 | |
71 ; | |
72 ; prior probability of a somatic snv or indel | |
73 ; | |
74 ssnvPrior = 0.000001 | |
75 sindelPrior = 0.000001 | |
76 | |
77 ; | |
78 ; probability of an snv or indel noise allele | |
79 ; | |
80 ; NB: in the calling model a noise allele is shared in tumor and | |
81 ; normal samples, but occurs at any frequency. | |
82 ; | |
83 ssnvNoise = 0.0000005 | |
84 sindelNoise = 0.000001 | |
85 | |
86 ; | |
87 ; Fraction of snv noise attributed to strand-bias. | |
88 ; | |
89 ; It is not recommended to change this setting. However, if it is | |
90 ; essential to turn the strand bias penalization off, the following is | |
91 ; recommended: | |
92 ; Assuming the current value of ssnvNoiseStrandBiasFrac is 0.5, | |
93 ; (1) set ssnvNoiseStrandBiasFrac = 0 | |
94 ; (2) divide the current ssnvNoise value by 2 | |
95 ; | |
96 ssnvNoiseStrandBiasFrac = 0.5 | |
97 | |
98 ; | |
99 ; minimum MAPQ score for PE reads at tier1: | |
100 ; | |
101 minTier1Mapq = 20 | |
102 | |
103 ; | |
104 ; minimum MAPQ score for PE and SE reads at tier2: | |
105 ; | |
106 minTier2Mapq = 5 | |
107 | |
108 ; | |
109 ; Somatic quality score (QSS_NT, NT=ref) below which somatic SNVs are | |
110 ; marked as filtered: | |
111 ; | |
112 ssnvQuality_LowerBound = 15 | |
113 | |
114 ; | |
115 ; Somatic quality score (QSI_NT, NT=ref) below which somatic indels | |
116 ; are marked as filtered: | |
117 ; | |
118 sindelQuality_LowerBound = 30 | |
119 | |
120 ; | |
121 ; Optionally write out read alignments which were altered during the | |
122 ; realignment step. At the completion of the workflow run, the | |
123 ; realigned reads can be found in: | |
124 ; | |
125 ; ${ANALYSIS_DIR}/realigned/{normal,tumor}.realigned.bam | |
126 ; | |
127 isWriteRealignedBam = 0 | |
128 | |
129 ; | |
130 ; Jobs are parallelized over segments of the reference genome no larger | |
131 ; than this size: | |
132 ; | |
133 binSize = 25000000 | |
134 | |
135 ; | |
136 ; Additional arguments passed to strelka. | |
137 ; | |
138 extraStrelkaArguments = | |
139 |