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Briefings in Bioinformatics|January 14, 2014
A bioinformatician's guide to the forefront of suffix array construction algorithmsAnish Man Singh Shrestha, Martin C Frith, Paul Horton
Bioinformatics (Oxford, England)|February 16, 2013
An approximate Bayesian approach for mapping paired-end DNA reads to a reference genomeAnish Man Singh Shrestha, Martin C Frith
BMC Bioinformatics|February 11, 2010
Parameters for accurate genome alignmentMartin C Frith, Michiaki Hamada, Paul Horton
Nucleic Acids Research|January 30, 2010
Incorporating sequence quality data into alignment improves DNA read mappingMartin C Frith, Raymond Wan, Paul Horton
Nucleic Acids Research|July 5, 2012
Mammalian NUMT insertion is non-randomJunko Tsuji, Martin C Frith, Kentaro Tomii, et al.
Nucleic Acids Research|December 6, 2011
RecountDB: a database of mapped and count corrected transcribed sequencesEdward Wijaya, Martin C Frith, Kiyoshi Asai, et al.
BMC Medical Genomics|April 27, 2018
EAGLE: Explicit Alternative Genome Likelihood EvaluatorTony Kuo, Martin C Frith, Jun Sese, et al.
Plos One|January 26, 2013
Finding protein-coding genes through human polymorphismsEdward Wijaya, Martin C Frith, Paul Horton, et al.
Genome Informatics. International Conference on Genome Informatics|February 25, 2010
Recount: expectation maximization based error correction tool for next generation sequencing dataEdward Wijaya, Martin C Frith, Yutaka Suzuki, et al.
Genome Research|January 7, 2011
Adaptive seeds tame genomic sequence comparisonSzymon M Kiełbasa, Raymond Wan, Kengo Sato, et al.
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