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jeremymcrae / clinical-filter / 136
87%

Build:
DEFAULT BRANCH: master
Ran 24 Nov 2016 04:55PM UTC
Jobs 2
Files 19
Run time 33s
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jeremymcrae
fix handling alt alleles with zero depth

Previously we mucked around with the HGNC and ENST lists, but I have
refactored this, so that we identify alt alleles with zero depth,
then mask them from the gene and consequence lists. This meant the
gene variant.genes and variant.consequence lists have now been
standardised as nested lists of lists, one entry per alt allele.

Unit tests have been updated, and I've check that this gives the
same variants as previous iterations.

1747 of 1979 relevant lines covered (88.28%)

1.76 hits per line

Jobs
ID Job ID Ran Files Coverage
1 136.1 24 Nov 2016 04:55PM UTC 0
88.28
Travis Job 136.1
2 136.2 24 Nov 2016 04:56PM UTC 0
88.18
Travis Job 136.2
Source Files on build 136
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