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Search Results to Michael Brudno

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Brudno, Michael

Item TypeName
Concept Software
Concept Software Validation
Academic Article PhenoTips: patient phenotyping software for clinical and research use.
Academic Article SCARPA: scaffolding reads with practical algorithms.
Academic Article VARiD: a variation detection framework for color-space and letter-space platforms.
Academic Article SHRiMP2: sensitive yet practical SHort Read Mapping.
Academic Article Automated whole-genome multiple alignment of rat, mouse, and human.
Academic Article FRESCO: flexible alignment with rectangle scoring schemes.
Academic Article The Human Phenotype Ontology in 2017.
Academic Article The Matchmaker Exchange: a platform for rare disease gene discovery.
Academic Article AGenDA: homology-based gene prediction.
Academic Article Harmonising phenomics information for a better interoperability in the rare disease field.
Academic Article VISTA : visualizing global DNA sequence alignments of arbitrary length.
Academic Article Fast and sensitive multiple alignment of large genomic sequences.
Academic Article Phylo-VISTA: interactive visualization of multiple DNA sequence alignments.
Academic Article Savant: genome browser for high-throughput sequencing data.
Academic Article Multiple whole genome alignments and novel biomedical applications at the VISTA portal.
Academic Article SHRiMP: accurate mapping of short color-space reads.
Academic Article Savant Genome Browser 2: visualization and analysis for population-scale genomics.
Academic Article PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases.
Academic Article The CHAOS/DIALIGN WWW server for multiple alignment of genomic sequences.
Academic Article Fast and sensitive alignment of large genomic sequences.
Academic Article GenomeVISTA--an integrated software package for whole-genome alignment and visualization.
Academic Article ProbCons: Probabilistic consistency-based multiple sequence alignment.
Academic Article Multiple whole-genome alignments without a reference organism.
Academic Article MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.
Academic Article Alignathon: a competitive assessment of whole-genome alignment methods.
Academic Article LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA.
Academic Article Detecting Alu insertions from high-throughput sequencing data.

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