1
88%
master: 89%

Ran 25 Apr 2016 09:09PM CUT

Files 14

Run time 0s

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Committed 25 Apr 2016 04:54PM CUT coverage: 87.867%. First build

Job # 122.1

Build Type

push

travis-ci

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Commit Message

Merge pull request #18 from hammerlab/trim-N-from-read-sequence

Trim 'N' from nucleotide sequences when creating VariantRead

Run Details

659 of 750 relevant lines covered (87.87%)

0.88 hits per line

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Search:

Coverage	File	Lines	Relevant	Covered	Missed	Hits/Line
76.81	isovar/read_at_locus.py	237	69	53	16	1.0
79.79	isovar/variant_read.py	339	94	75	19	1.0
82.47	isovar/reference_context.py	451	97	80	17	1.0
86.18	isovar/translation.py	649	123	106	17	1.0
87.8	isovar/variant_sequence.py	229	41	36	5	1.0
88.24	isovar/nucleotide_counts.py	109	34	30	4	1.0
90.7	isovar/common.py	100	43	39	4	1.0
93.02	isovar/variant_helpers.py	185	43	40	3	1.0
94.37	isovar/assembly.py	146	71	67	4	1.0
95.45	isovar/dataframe_builder.py	128	44	42	2	1.0

Showing 1 to 10 of 14 entries