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Bioinformatics (Oxford, England)
|
August 31, 2014
Frameshift alignment: statistics and post-genomic applications
Sergey 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 sequences
Michiaki 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 deletions
Anish 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 flanks
Martin 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 reads
Satomi Mitsuhashi, Sachiko Ohori, Kazutaka Katoh, et al.
Plos Computational Biology
|
April 26, 2008
Discovering sequence motifs with arbitrary insertions and deletions
Martin C Frith, Neil F W Saunders, Bostjan Kobe, et al.
Genome Research
|
January 7, 2011
Adaptive seeds tame genomic sequence comparison
Szymon M Kiełbasa, Raymond Wan, Kengo Sato, et al.
Genome Research
|
November 23, 2007
A code for transcription initiation in mammalian genomes
Martin C Frith, Eivind Valen, Anders Krogh, et al.
Nucleic Acids Research
|
February 28, 2004
Detection of functional DNA motifs via statistical over-representation
Martin 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 cells
Satomi Mitsuhashi, So Nakagawa, Mitsuru Sasaki-Honda, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 91) with videos related to
Sort By:
Page
of 10
Bioinformatics (Oxford, England)
|
August 31, 2014
Frameshift alignment: statistics and post-genomic applications
Sergey 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 sequences
Michiaki 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 deletions
Anish 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 flanks
Martin 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 reads
Satomi Mitsuhashi, Sachiko Ohori, Kazutaka Katoh, et al.
Plos Computational Biology
|
April 26, 2008
Discovering sequence motifs with arbitrary insertions and deletions
Martin C Frith, Neil F W Saunders, Bostjan Kobe, et al.
Genome Research
|
January 7, 2011
Adaptive seeds tame genomic sequence comparison
Szymon M Kiełbasa, Raymond Wan, Kengo Sato, et al.
Genome Research
|
November 23, 2007
A code for transcription initiation in mammalian genomes
Martin C Frith, Eivind Valen, Anders Krogh, et al.
Nucleic Acids Research
|
February 28, 2004
Detection of functional DNA motifs via statistical over-representation
Martin 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 cells
Satomi Mitsuhashi, So Nakagawa, Mitsuru Sasaki-Honda, et al.
Page
of 10