Clinical-Genomics / cgbeacon2 / 338 / 1
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coverage: 96.984%. Remained the same
TRAVIS=1

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Merge pull request #62 from Clinical-Genomics/snvs_variantTypes

Save also non-SV variants datatypes (SNP, INDEL) info to database

804 of 829 relevant lines covered (96.98%)

0.97 hits per line

Source Files on job 338.1 (TRAVIS=1)