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Martin C Frith

Showing results (31-40 of 91) with videos related to

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Bioinformatics (Oxford, England)|January 26, 2023
How to optimally sample a sequence for rapid analysisMartin C Frith, Jim Shaw, John L Spouge
European Journal of Human Genetics : EJHG|June 23, 2005
The amazing complexity of the human transcriptomeMartin C Frith, Michael Pheasant, John S Mattick
Bioinformatics (Oxford, England)|October 7, 2011
Probabilistic alignments with quality scores: an application to short-read mapping toward accurate SNP/indel detectionMichiaki Hamada, Edward Wijaya, Martin C Frith, et al.
Nucleic Acids Research|July 5, 2012
Mammalian NUMT insertion is non-randomJunko Tsuji, Martin C Frith, Kentaro Tomii, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|March 25, 2026
Simple and Thorough Detection of Related Sequences with Position-Varying Probabilities of Substitutions, Insertions, and DeletionsMartin C Frith, Patrick Boppert, Patrick Styll, 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.
Trends in Genetics : TIG|November 18, 2005
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of functionKen C Pang, Martin C Frith, John S Mattick
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.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
Bioinformatics (Oxford, England)|January 26, 2023
How to optimally sample a sequence for rapid analysisMartin C Frith, Jim Shaw, John L Spouge
European Journal of Human Genetics : EJHG|June 23, 2005
The amazing complexity of the human transcriptomeMartin C Frith, Michael Pheasant, John S Mattick
Bioinformatics (Oxford, England)|October 7, 2011
Probabilistic alignments with quality scores: an application to short-read mapping toward accurate SNP/indel detectionMichiaki Hamada, Edward Wijaya, Martin C Frith, et al.
Nucleic Acids Research|July 5, 2012
Mammalian NUMT insertion is non-randomJunko Tsuji, Martin C Frith, Kentaro Tomii, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|March 25, 2026
Simple and Thorough Detection of Related Sequences with Position-Varying Probabilities of Substitutions, Insertions, and DeletionsMartin C Frith, Patrick Boppert, Patrick Styll, 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.
Trends in Genetics : TIG|November 18, 2005
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of functionKen C Pang, Martin C Frith, John S Mattick
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.
Pageof 10