Pages that link to "Q110344467"

The following pages link to Sebastian Bauer (Q110344467):

Displaying 26 items.

• Improved exome prioritization of disease genes through cross-species phenotype comparison (Q23815226) (← links)
• Clinical diagnostics in human genetics with semantic similarity searches in ontologies (Q24657971) (← links)
• The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data (Q27927005) (← links)
• Ontologizer 2.0--a multifunctional tool for GO term enrichment analysis and data exploration (Q31156999) (← links)
• Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep (Q33248963) (← links)
• Microindel detection in short-read sequence data (Q33530434) (← links)
• GOing Bayesian: model-based gene set analysis of genome-scale data (Q33532968) (← links)
• Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome (Q33677104) (← links)
• Integrative analysis of genomic, functional and protein interaction data predicts long-range enhancer-target gene interactions (Q33756305) (← links)
• Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders (Q33806845) (← links)
• Improving ontologies by automatic reasoning and evaluation of logical definitions (Q34060065) (← links)
• Exact score distribution computation for ontological similarity searches. (Q34073150) (← links)
• The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process (Q34086362) (← links)
• Deletions of chromosomal regulatory boundaries are associated with congenital disease (Q34271260) (← links)
• Jannovar: a java library for exome annotation (Q34412573) (← links)
• The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease (Q34865360) (← links)
• Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish (Q36683045) (← links)
• Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research (Q38439017) (← links)
• Bayesian ontology querying for accurate and noise-tolerant semantic searches (Q38467048) (← links)
• Model-based gene set analysis for Bioconductor (Q38502366) (← links)
• Improved detection of overrepresentation of Gene-Ontology annotations with parent child analysis (Q38515564) (← links)
• Walking the interactome for prioritization of candidate disease genes (Q39140568) (← links)
• Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts (Q39877678) (← links)
• A short ultraconserved sequence drives transcription from an alternate FBN1 promoter (Q42521362) (← links)
• The generalised k-Truncated Suffix Tree for time-and space-efficient searches in multiple DNA or protein sequences (Q51892640) (← links)
• Short ultraconserved promoter regions delineate a class of preferentially expressed alternatively spliced transcripts. (Q51928729) (← links)