Published in Bioinformatics on December 18, 2008
VNTRseek-a computational tool to detect tandem repeat variants in high-throughput sequencing data. Nucleic Acids Res (2014) 0.98
SANS: high-throughput retrieval of protein sequences allowing 50% mismatches. Bioinformatics (2012) 0.89
Cgaln: fast and space-efficient whole-genome alignment. BMC Bioinformatics (2010) 0.77
Hit integration for identifying optimal spaced seeds. BMC Bioinformatics (2010) 0.76
Best hits of 11110110111: model-free selection and parameter-free sensitivity calculation of spaced seeds. Algorithms Mol Biol (2017) 0.75
Inverted repeat structure of the human genome: the X-chromosome contains a preponderance of large, highly homologous inverted repeats that contain testes genes. Genome Res (2004) 3.09
Replication and compartmentalization of HIV-1 in kidney epithelium of patients with HIV-associated nephropathy. Nat Med (2002) 2.10
TRDB--the Tandem Repeats Database. Nucleic Acids Res (2006) 1.57
Predicting human minisatellite polymorphism. Genome Res (2003) 1.44
Editorial. Nucleic Acids Research annual Web Server Issue in 2010. Nucleic Acids Res (2010) 1.42
Evolutionary history of mammalian transposons determined by genome-wide defragmentation. PLoS Comput Biol (2007) 1.38
GlycReSoft: a software package for automated recognition of glycans from LC/MS data. PLoS One (2012) 1.24
Mutation Master: profiles of substitutions in hepatitis C virus RNA of the core, alternate reading frame, and NS2 coding regions. RNA (2002) 1.13
Oligonucleotide fingerprint identification for microarray-based pathogen diagnostic assays. Bioinformatics (2006) 1.08
Tandem repeats over the edit distance. Bioinformatics (2007) 1.03
Whole genome sequences of a male and female supercentenarian, ages greater than 114 years. Front Genet (2012) 1.01
Mutations in the hepatitis C virus core gene are associated with advanced liver disease and hepatocellular carcinoma. Clin Cancer Res (2009) 0.99
Elevated basal slippage mutation rates among the Canidae. J Hered (2007) 0.97
The acute management of haemorrhage, surgery and overdose in patients receiving dabigatran. Emerg Med J (2013) 0.95
Clinical PathoScope: rapid alignment and filtration for accurate pathogen identification in clinical samples using unassembled sequencing data. BMC Bioinformatics (2014) 0.90
3'-UTR SIRF: a database for identifying clusters of whort interspersed repeats in 3' untranslated regions. BMC Bioinformatics (2007) 0.88
Evaluating distance functions for clustering tandem repeats. Genome Inform (2005) 0.87
The distribution of inverted repeat sequences in the Saccharomyces cerevisiae genome. Curr Genet (2010) 0.85
Investigation of the population structure of Legionella pneumophila by analysis of tandem repeat copy number and internal sequence variation. Microbiology (2011) 0.84
Targeted analysis of glycomics liquid chromatography/mass spectrometry data. Anal Bioanal Chem (2010) 0.83
Beyond patient benefit: clinical development in hemophilia. Hematology (2012) 0.82
Editorial: Nucleic Acids Research annual Web Server Issue in 2015. Nucleic Acids Res (2015) 0.78
Indel seeds for homology search. Bioinformatics (2006) 0.78
Switching treatments in haemophilia: is there a risk of inhibitor development? Eur J Haematol (2014) 0.75
Minimal entropy probability paths between genome families. J Math Biol (2003) 0.75
Mining poly-regions in DNA. Int J Data Min Bioinform (2012) 0.75
Rationale for individualizing haemophilia care. Blood Coagul Fibrinolysis (2015) 0.75