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Bioinformatics (Oxford, England)
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January 26, 2023
How to optimally sample a sequence for rapid analysis
Martin C Frith, Jim Shaw, John L Spouge
European Journal of Human Genetics : EJHG
|
June 23, 2005
The amazing complexity of the human transcriptome
Martin 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 detection
Michiaki Hamada, Edward Wijaya, Martin C Frith, et al.
Nucleic Acids Research
|
July 5, 2012
Mammalian NUMT insertion is non-random
Junko 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 Deletions
Martin C Frith, Patrick Boppert, Patrick Styll, et al.
Nucleic Acids Research
|
December 6, 2011
RecountDB: a database of mapped and count corrected transcribed sequences
Edward Wijaya, Martin C Frith, Kiyoshi Asai, et al.
BMC Medical Genomics
|
April 27, 2018
EAGLE: Explicit Alternative Genome Likelihood Evaluator
Tony 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 function
Ken C Pang, Martin C Frith, John S Mattick
Plos One
|
January 26, 2013
Finding protein-coding genes through human polymorphisms
Edward 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 data
Edward Wijaya, Martin C Frith, Yutaka Suzuki, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 91) with videos related to
Sort By:
Page
of 10
Bioinformatics (Oxford, England)
|
January 26, 2023
How to optimally sample a sequence for rapid analysis
Martin C Frith, Jim Shaw, John L Spouge
European Journal of Human Genetics : EJHG
|
June 23, 2005
The amazing complexity of the human transcriptome
Martin 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 detection
Michiaki Hamada, Edward Wijaya, Martin C Frith, et al.
Nucleic Acids Research
|
July 5, 2012
Mammalian NUMT insertion is non-random
Junko 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 Deletions
Martin C Frith, Patrick Boppert, Patrick Styll, et al.
Nucleic Acids Research
|
December 6, 2011
RecountDB: a database of mapped and count corrected transcribed sequences
Edward Wijaya, Martin C Frith, Kiyoshi Asai, et al.
BMC Medical Genomics
|
April 27, 2018
EAGLE: Explicit Alternative Genome Likelihood Evaluator
Tony 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 function
Ken C Pang, Martin C Frith, John S Mattick
Plos One
|
January 26, 2013
Finding protein-coding genes through human polymorphisms
Edward 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 data
Edward Wijaya, Martin C Frith, Yutaka Suzuki, et al.
Page
of 10