Pages that link to "Q47134065"
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The following pages link to Martin C Frith (Q47134065):
Displaying 50 items.
- Adaptive seeds tame genomic sequence comparison (Q24614485) (← links)
- A code for transcription initiation in mammalian genomes (Q24681483) (← links)
- The transcriptional landscape of the mammalian genome (Q27861110) (← links)
- Assessing computational tools for the discovery of transcription factor binding sites (Q28301463) (← links)
- Frameshift alignment: statistics and post-genomic applications (Q28650499) (← links)
- Explaining the correlations among properties of mammalian promoters (Q28658161) (← links)
- Detection of functional DNA motifs via statistical over-representation (Q28775981) (← links)
- Genome-wide analysis of mammalian promoter architecture and evolution (Q29616717) (← links)
- Protein sequence-similarity search acceleration using a heuristic algorithm with a sensitive matrix (Q30397440) (← links)
- Adding unaligned sequences into an existing alignment using MAFFT and LAST. (Q30529228) (← links)
- A bioinformatician's guide to the forefront of suffix array construction algorithms (Q30574133) (← links)
- RecountDB: a database of mapped and count corrected transcribed sequences. (Q31042913) (← links)
- Large-scale clustering of CAGE tag expression data (Q31113350) (← links)
- Characterization of genomic organization of the adenosine A2A receptor gene by molecular and bioinformatics analyses (Q33200599) (← links)
- Pseudo-messenger RNA: phantoms of the transcriptome (Q33242807) (← links)
- Clusters of internally primed transcripts reveal novel long noncoding RNAs (Q33242811) (← links)
- The abundance of short proteins in the mammalian proteome (Q33242818) (← links)
- Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs (Q33242821) (← links)
- Evolutionary turnover of mammalian transcription start sites (Q33243036) (← links)
- Informatic and genomic analysis of melanocyte cDNA libraries as a resource for the study of melanocyte development and function (Q33285294) (← links)
- Discovering sequence motifs with arbitrary insertions and deletions (Q33330862) (← links)
- Splicing bypasses 3' end formation signals to allow complex gene architectures (Q33344670) (← links)
- Incorporating sequence quality data into alignment improves DNA read mapping (Q33527204) (← links)
- RECLU: a pipeline to discover reproducible transcriptional start sites and their alternative regulation using capped analysis of gene expression (CAGE). (Q33642251) (← links)
- Variable-order sequence modeling improves bacterial strain discrimination for Ion Torrent DNA reads. (Q33792134) (← links)
- Serotyping dengue virus with isothermal amplification and a portable sequencer (Q33799483) (← links)
- Inferring transcription factor complexes from ChIP-seq data (Q33908006) (← links)
- Gentle masking of low-complexity sequences improves homology search (Q34113629) (← links)
- Experimental validation of the regulated expression of large numbers of non-coding RNAs from the mouse genome (Q34324184) (← links)
- Statistical significance of clusters of motifs represented by position specific scoring matrices in nucleotide sequences (Q34327872) (← links)
- A promoter-level mammalian expression atlas (Q34412203) (← links)
- Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function (Q34467942) (← links)
- Finding protein-coding genes through human polymorphisms (Q34562753) (← links)
- Pseudocounts for transcription factor binding sites. (Q34910288) (← links)
- CentroidHomfold-LAST: accurate prediction of RNA secondary structure using automatically collected homologous sequences (Q35075543) (← links)
- Genomic targets of nuclear estrogen receptors (Q35697315) (← links)
- Split-alignment of genomes finds orthologies more accurately. (Q35730826) (← links)
- ALP & FALP: C libraries for pairwise local alignment E-values (Q35795787) (← links)
- An approximate Bayesian approach for mapping paired-end DNA reads to a reference genome (Q36761217) (← links)
- The whole alignment and nothing but the alignment: the problem of spurious alignment flanks. (Q36935417) (← links)
- Finding functional sequence elements by multiple local alignment (Q37068067) (← links)
- Improved search heuristics find 20,000 new alignments between human and mouse genomes (Q37701308) (← links)
- Training alignment parameters for arbitrary sequencers with LAST-TRAIN. (Q37701435) (← links)
- CARRIE web service: automated transcriptional regulatory network inference and interactive analysis (Q38339717) (← links)
- Theatre: A software tool for detailed comparative analysis and visualization of genomic sequence. (Q39804043) (← links)
- Cluster-Buster: Finding dense clusters of motifs in DNA sequences. (Q39804240) (← links)
- Dynamic usage of transcription start sites within core promoters (Q41902392) (← links)
- Discrimination of non-protein-coding transcripts from protein-coding mRNA. (Q42603941) (← links)
- A new repeat-masking method enables specific detection of homologous sequences (Q42635759) (← links)
- Nanopore-based single molecule sequencing of the D4Z4 array responsible for facioscapulohumeral muscular dystrophy. (Q47097491) (← links)