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Martin C Frith

Showing results (51-60 of 91) with videos related to

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Bioinformatics (Oxford, England)|August 31, 2014
Frameshift alignment: statistics and post-genomic applicationsSergey L Sheetlin, Yonil Park, Martin C Frith, et al.
Nucleic Acids Research|May 14, 2011
CentroidHomfold-LAST: accurate prediction of RNA secondary structure using automatically collected homologous sequencesMichiaki Hamada, Koichiro Yamada, Kengo Sato, et al.
Nucleic Acids Research|November 29, 2017
Jointly aligning a group of DNA reads improves accuracy of identifying large deletionsAnish M S Shrestha, Martin C Frith, Kiyoshi Asai, et al.
Nucleic Acids Research|September 18, 2008
The whole alignment and nothing but the alignment: the problem of spurious alignment flanksMartin C Frith, Yonil Park, Sergey L Sheetlin, et al.
Genome Medicine|August 1, 2020
A pipeline for complete characterization of complex germline rearrangements from long DNA readsSatomi Mitsuhashi, Sachiko Ohori, Kazutaka Katoh, et al.
Plos Computational Biology|April 26, 2008
Discovering sequence motifs with arbitrary insertions and deletionsMartin C Frith, Neil F W Saunders, Bostjan Kobe, et al.
Genome Research|January 7, 2011
Adaptive seeds tame genomic sequence comparisonSzymon M Kiełbasa, Raymond Wan, Kengo Sato, et al.
Genome Research|November 23, 2007
A code for transcription initiation in mammalian genomesMartin C Frith, Eivind Valen, Anders Krogh, et al.
Nucleic Acids Research|February 28, 2004
Detection of functional DNA motifs via statistical over-representationMartin C Frith, Yutao Fu, Liqun Yu, et al.
Human Molecular Genetics|March 11, 2021
Nanopore direct RNA sequencing detects DUX4-activated repeats and isoforms in human muscle cellsSatomi Mitsuhashi, So Nakagawa, Mitsuru Sasaki-Honda, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
Bioinformatics (Oxford, England)|August 31, 2014
Frameshift alignment: statistics and post-genomic applicationsSergey L Sheetlin, Yonil Park, Martin C Frith, et al.
Nucleic Acids Research|May 14, 2011
CentroidHomfold-LAST: accurate prediction of RNA secondary structure using automatically collected homologous sequencesMichiaki Hamada, Koichiro Yamada, Kengo Sato, et al.
Nucleic Acids Research|November 29, 2017
Jointly aligning a group of DNA reads improves accuracy of identifying large deletionsAnish M S Shrestha, Martin C Frith, Kiyoshi Asai, et al.
Nucleic Acids Research|September 18, 2008
The whole alignment and nothing but the alignment: the problem of spurious alignment flanksMartin C Frith, Yonil Park, Sergey L Sheetlin, et al.
Genome Medicine|August 1, 2020
A pipeline for complete characterization of complex germline rearrangements from long DNA readsSatomi Mitsuhashi, Sachiko Ohori, Kazutaka Katoh, et al.
Plos Computational Biology|April 26, 2008
Discovering sequence motifs with arbitrary insertions and deletionsMartin C Frith, Neil F W Saunders, Bostjan Kobe, et al.
Genome Research|January 7, 2011
Adaptive seeds tame genomic sequence comparisonSzymon M Kiełbasa, Raymond Wan, Kengo Sato, et al.
Genome Research|November 23, 2007
A code for transcription initiation in mammalian genomesMartin C Frith, Eivind Valen, Anders Krogh, et al.
Nucleic Acids Research|February 28, 2004
Detection of functional DNA motifs via statistical over-representationMartin C Frith, Yutao Fu, Liqun Yu, et al.
Human Molecular Genetics|March 11, 2021
Nanopore direct RNA sequencing detects DUX4-activated repeats and isoforms in human muscle cellsSatomi Mitsuhashi, So Nakagawa, Mitsuru Sasaki-Honda, et al.
Pageof 10