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35 {
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37 "name": "VCF file of known variants (dbSNP)"
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38 }
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51 "user_outputs": []
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52 },
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53 "2": {
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54 "annotation": "These are locations other than those in dbSNP. This could include variants from the subject normal tissue. \nThe ID will be used to annotate the Variants dataset, and then can be filtered out. There needs to be at least one entry for each chromosome: (M,1,2,...,X,Y)",
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55 "id": 2,
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56 "input_connections": {},
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58 {
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60 "name": "VCF file of additional known variants "
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