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Kurt Gaastra
Kurt Gaastra
DNA sequencing
Bioinformatics
False positive paradox
Exome sequencing
Indel
4
Papers
213
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Abstract 3576: Accurate identification of somatic mutations in cancer patient specimens in the lack of normal tissue by targeted high-throughput sequencing
2017
Cancer Research
Francisco M. Vega
Sean Alistair Irvine
David Ware
Kurt Gaastra
Yannick Pouiliot
Len Trigg
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Comparing Variant Call Files for Performance Benchmarking of Next-Generation Sequencing Variant Calling Pipelines
2015
bioRxiv
John G. Cleary
Ross Braithwaite
Kurt Gaastra
Brian Hilbush
Stuart J. Inglis
Sean Alistair Irvine
Alan Timothy Jon Jackson
Richard Littin
Mehul Rathod
David Ware
Justin M. Zook
Len Trigg
Francisco M. De La Vega
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Citations (109)
Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data
2014
Journal of Computational Biology
John G. Cleary
Ross Braithwaite
Kurt Gaastra
Brian S. Hilbush
Stuart John Inglis
Sean A. Irvine
Alan Jackson
Richard Littin
Sahar Nohzadeh-Malakshah
Mehul Rathod
David Ware
Len Trigg
Francisco M. De La Vega
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Citations (62)
Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data
2014
Journal of Computational Biology
John G Cleary
Ross Braithwaite
Kurt Gaastra
Brian S. Hilbush
Stuart John Inglis
Sean A. Irvine
Alan Jackson
Richard Littin
Sahar Nohzadeh-Malakshah
Minita Shah
Mehul Rathod
David Ware
Len Trigg
Francisco M. De La Vega
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Citations (42)
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