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Nucleic Acids Research
|
March 30, 2012
A mostly traditional approach improves alignment of bisulfite-converted DNA
Martin C Frith, Ryota Mori, Kiyoshi Asai
Bioinformatics (Oxford, England)
|
February 16, 2013
An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome
Anish Man Singh Shrestha, Martin C Frith
Bioinformatics Advances
|
February 23, 2023
An immune-suppressing protein in human endogenous retroviruses
Huan Zhang, Shengliang Ni, Martin C Frith
Bioinformatics (Oxford, England)
|
December 21, 2020
Minimally overlapping words for sequence similarity search
Martin C Frith, Laurent Noé, Gregory Kucherov
Nucleic Acids Research
|
December 25, 2008
Pseudocounts for transcription factor binding sites
Keishin Nishida, Martin C Frith, Kenta Nakai
Methods in Molecular Biology (Clifton, N.J.)
|
December 8, 2020
lamassemble: Multiple Alignment and Consensus Sequence of Long Reads
Martin C Frith, Satomi Mitsuhashi, Kazutaka Katoh
BMC Medical Genomics
|
January 8, 2021
Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general population
Satomi Mitsuhashi, Martin C Frith, Naomichi Matsumoto
IEEE/ACM Transactions on Computational Biology and Bioinformatics
|
July 12, 2018
A Simplified Description of Child Tables for Sequence Similarity Search
Martin C Frith, Anish M S Shrestha
Nucleic Acids Research
|
June 26, 2003
Cluster-Buster: Finding dense clusters of motifs in DNA sequences
Martin C Frith, Michael C Li, Zhiping Weng
Nucleic Acids Research
|
June 25, 2004
CARRIE web service: automated transcriptional regulatory network inference and interactive analysis
Peter M Haverty, Martin C Frith, Zhiping Weng
Page
of 10
Search research articles
Search
Showing results (21-30 of 91) with videos related to
Sort By:
Page
of 10
Nucleic Acids Research
|
March 30, 2012
A mostly traditional approach improves alignment of bisulfite-converted DNA
Martin C Frith, Ryota Mori, Kiyoshi Asai
Bioinformatics (Oxford, England)
|
February 16, 2013
An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome
Anish Man Singh Shrestha, Martin C Frith
Bioinformatics Advances
|
February 23, 2023
An immune-suppressing protein in human endogenous retroviruses
Huan Zhang, Shengliang Ni, Martin C Frith
Bioinformatics (Oxford, England)
|
December 21, 2020
Minimally overlapping words for sequence similarity search
Martin C Frith, Laurent Noé, Gregory Kucherov
Nucleic Acids Research
|
December 25, 2008
Pseudocounts for transcription factor binding sites
Keishin Nishida, Martin C Frith, Kenta Nakai
Methods in Molecular Biology (Clifton, N.J.)
|
December 8, 2020
lamassemble: Multiple Alignment and Consensus Sequence of Long Reads
Martin C Frith, Satomi Mitsuhashi, Kazutaka Katoh
BMC Medical Genomics
|
January 8, 2021
Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general population
Satomi Mitsuhashi, Martin C Frith, Naomichi Matsumoto
IEEE/ACM Transactions on Computational Biology and Bioinformatics
|
July 12, 2018
A Simplified Description of Child Tables for Sequence Similarity Search
Martin C Frith, Anish M S Shrestha
Nucleic Acids Research
|
June 26, 2003
Cluster-Buster: Finding dense clusters of motifs in DNA sequences
Martin C Frith, Michael C Li, Zhiping Weng
Nucleic Acids Research
|
June 25, 2004
CARRIE web service: automated transcriptional regulatory network inference and interactive analysis
Peter M Haverty, Martin C Frith, Zhiping Weng
Page
of 10