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Q30653786-3A18D471-603F-40F3-9AFA-D5EA84F25DE3
Q30653786-3A18D471-603F-40F3-9AFA-D5EA84F25DE3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30653786-3A18D471-603F-40F3-9AFA-D5EA84F25DE3
A practical method to detect SNVs and indels from whole genome and exome sequencing data.
P2860
Q30653786-3A18D471-603F-40F3-9AFA-D5EA84F25DE3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30653786-3A18D471-603F-40F3-9AFA-D5EA84F25DE3
rank
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type
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Statement
wasDerivedFrom
12342af6f7a5ca8c24460b5cae3b7a11e57e6944
P2860
Natural genetic variation caused by small insertions and deletions in the human genome