A new repeat-masking method enables specific detection of homologous sequences

Por Frith, Martin C.
Publicado em 2011

Gentle Masking of Low-Complexity Sequences Improves Homology Search

Por Frith, Martin C.
Publicado em 2011

Explaining the correlations among properties of mammalian promoters

Por Frith, Martin C.
Publicado em 2014

Adding unaligned sequences into an existing alignment using MAFFT and LAST

Por Katoh, Kazutaka, Frith, Martin C.
Publicado em 2012

Improved search heuristics find 20 000 new alignments between human and mouse genomes

Por Frith, Martin C., Noé, Laurent
Publicado em 2014

Split-alignment of genomes finds orthologies more accurately

Por Frith, Martin C, Kawaguchi, Risa
Publicado no Genome Biol (2015)

Pseudocounts for transcription factor binding sites

Por Nishida, Keishin, Frith, Martin C., Nakai, Kenta
Publicado em 2009

Incorporating sequence quality data into alignment improves DNA read mapping

Por Frith, Martin C., Wan, Raymond, Horton, Paul
Publicado em 2010

Parameters for accurate genome alignment

Por Frith, Martin C, Hamada, Michiaki, Horton, Paul
Publicado em 2010

A mostly traditional approach improves alignment of bisulfite-converted DNA

Por Frith, Martin C., Mori, Ryota, Asai, Kiyoshi
Publicado em 2012

An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome

Por Shrestha, Anish Man Singh, Frith, Martin C.
Publicado em 2013

Cluster-Buster: finding dense clusters of motifs in DNA sequences

Por Frith, Martin C., Li, Michael C., Weng, Zhiping
Publicado em 2003

CARRIE web service: automated transcriptional regulatory network inference and interactive analysis

Por Haverty, Peter M., Frith, Martin C., Weng, Zhiping
Publicado em 2004

RecountDB: a database of mapped and count corrected transcribed sequences

Por Wijaya, Edward, Frith, Martin C., Asai, Kiyoshi, Horton, Paul
Publicado em 2012

Mammalian NUMT insertion is non-random

Por Tsuji, Junko, Frith, Martin C., Tomii, Kentaro, Horton, Paul
Publicado em 2012

Finding Protein-Coding Genes through Human Polymorphisms

Por Wijaya, Edward, Frith, Martin C., Horton, Paul, Asai, Kiyoshi
Publicado em 2013

A bioinformatician’s guide to the forefront of suffix array construction algorithms

Por Shrestha, Anish Man Singh, Frith, Martin C., Horton, Paul
Publicado em 2014

Statistical significance of clusters of motifs represented by position specific scoring matrices in nucleotide sequences

Por Frith, Martin C., Spouge, John L., Hansen, Ulla, Weng, Zhiping
Publicado em 2002

Finding functional sequence elements by multiple local alignment

Por Frith, Martin C., Hansen, Ulla, Spouge, John L., Weng, Zhiping
Publicado em 2004

MotifViz: an analysis and visualization tool for motif discovery

Por Fu, Yutao, Frith, Martin C., Haverty, Peter M., Weng, Zhiping
Publicado em 2004