Pages that link to "Q36079385"
Jump to navigation
Jump to search
The following pages link to Patterns of nucleotide substitution, insertion and deletion in the human genome inferred from pseudogenes (Q36079385):
Displaying 50 items.
- Single nucleotide polymorphism-based validation of exonic splicing enhancers (Q21092824) (← links)
- Genome-wide survey for biologically functional pseudogenes (Q21145686) (← links)
- Logarithmic gap costs decrease alignment accuracy (Q21284244) (← links)
- Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution (Q22065739) (← links)
- Climbing Mount Probable: Mutation as a Cause of Nonrandomness in Evolution (Q22066030) (← links)
- Positive selection acting on splicing motifs reflects compensatory evolution (Q24646896) (← links)
- Pseudogene.org: a comprehensive database and comparison platform for pseudogene annotation (Q24675776) (← links)
- Transition-transversion bias is not universal: a counter example from grasshopper pseudogenes (Q28469124) (← links)
- Novel Conserved Genotypes Correspond to Antibiotic Resistance Phenotypes of E. coli Clinical Isolates (Q28534076) (← links)
- Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data (Q28659873) (← links)
- Analysis of genomic variation in non-coding elements using population-scale sequencing data from the 1000 Genomes Project (Q28740767) (← links)
- Segmental duplications in the human genome reveal details of pseudogene formation (Q28748496) (← links)
- Using semantic web rules to reason on an ontology of pseudogenes (Q28751723) (← links)
- Genomic evidence for non-random endemic populations of decaying exons from mammalian genes (Q28752089) (← links)
- Pseudofam: the pseudogene families database (Q28754290) (← links)
- Analysis of the role of retrotransposition in gene evolution in vertebrates (Q28756796) (← links)
- Millions of years of evolution preserved: a comprehensive catalog of the processed pseudogenes in the human genome (Q28775887) (← links)
- Evolution of protein indels in plants, animals and fungi. (Q30351880) (← links)
- The combined effects of amino acid substitutions and indels on the evolution of structure within protein families (Q30397808) (← links)
- Optimization of sequence alignment for simple sequence repeat regions. (Q30503639) (← links)
- Comparison of insertion/deletion calling algorithms on human next-generation sequencing data (Q30872524) (← links)
- The functional genomic distribution of protein divergence in two animal phyla: coevolution, genomic conflict, and constraint (Q33202576) (← links)
- MCALIGN2: faster, accurate global pairwise alignment of non-coding DNA sequences based on explicit models of indel evolution (Q33246179) (← links)
- Long-term trends in evolution of indels in protein sequences (Q33273715) (← links)
- Sequence divergence of Mus spretus and Mus musculus across a skin cancer susceptibility locus (Q33395513) (← links)
- Phylogenetic inference under varying proportions of indel-induced alignment gaps (Q33495765) (← links)
- Extreme mutation bias and high AT content in Plasmodium falciparum (Q33558392) (← links)
- The herpevac trial for women: Sequence analysis of glycoproteins from viruses obtained from infected subjects. (Q33610941) (← links)
- Trichinella pseudospiralis vs. T. spiralis thymidylate synthase gene structure and T. pseudospiralis thymidylate synthase retrogene sequence. (Q33616540) (← links)
- Identification of human short introns (Q33698861) (← links)
- Algebraic Distribution of Segmental Duplication Lengths in Whole-Genome Sequence Self-Alignments (Q33968013) (← links)
- Performance comparison of exome DNA sequencing technologies (Q34023426) (← links)
- Human base excision repair creates a bias toward -1 frameshift mutations (Q34055705) (← links)
- Genome-wide characterization of insertion and deletion variation in chicken using next generation sequencing. (Q34061405) (← links)
- An algorithm for the reconstruction of consensus sequences of ancient segmental duplications and transposon copies in eukaryotic genomes (Q34100850) (← links)
- Mutation biases and mutation rate variation around very short human microsatellites revealed by human-chimpanzee-orangutan genomic sequence alignments (Q34130760) (← links)
- Mitochondrial pseudogenes in the nuclear genomes of Drosophila (Q34193247) (← links)
- Granaticins and their biosynthetic gene cluster from Streptomyces vietnamensis: evidence of horizontal gene transfer (Q34197910) (← links)
- Analysis of insertion-deletion from deep-sequencing data: software evaluation for optimal detection (Q34307443) (← links)
- Rapid sequence and expression divergence suggest selection for novel function in primate-specific KRAB-ZNF genes (Q34310586) (← links)
- Frequency of gaps observed in a structurally aligned protein pair database suggests a simple gap penalty function (Q34334107) (← links)
- Discovery of mutations in Saccharomyces cerevisiae by pooled linkage analysis and whole-genome sequencing (Q34386830) (← links)
- Confidence-based somatic mutation evaluation and prioritization (Q34426398) (← links)
- The tree alignment problem (Q34472525) (← links)
- Mutationism and the dual causation of evolutionary change (Q34523907) (← links)
- INDELible: a flexible simulator of biological sequence evolution (Q34979731) (← links)
- Bioinformatics challenges for personalized medicine (Q35051893) (← links)
- Mutation rate distribution inferred from coincident SNPs and coincident substitutions (Q35211692) (← links)
- On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease (Q35226155) (← links)
- Human-specific insertions and deletions inferred from mammalian genome sequences (Q35251230) (← links)