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OpenHelix

Tools for Comparative Genomics

Tutorial and training materials by OpenHelix

Learn to use VISTA from the Genomics Division of Lawrence Berkeley National Laboratory. VISTA provides a way to examine the data from many genomes, with extensive annotation for various data types including known genes, predicted genes, SNPs, comparative multi-species analysis and much more. VISTA also contains excellent sequence alignment and visualization tools with capacity for long sequences. Use VISTA as a primary resource for your comparative genomics research needs.
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You'll learn:

  • how to examine pre-computed relationships among a variety of species
  • ways of submitting and analyzing sequences of your own in VISTA
  • how to discover possible regulatory transcription factor binding sites in your favorite genes
  • to compare genomic sequences with customizable graphical representations and many other output options


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Recent BioMed Central research articles citing this resource

Huang Hui et al., Thirteen Camellia chloroplast genome sequences determined by high-throughput sequencing: genome structure and phylogenetic relationships Genome evolution and evolutionary systems biology. BMC Evolutionary Biology (2014) doi:10.1186/1471-2148-14-151

Jabbar Sana et al., VISTA: achieving cumulative VIsion through energy efficient Silhouette recognition of mobile Targets through collAboration of visual sensor nodes Regular submissions. EURASIP Journal on Image and Video Processing (2014) doi:10.1186/1687-5281-2014-32

Eckler J Matthew et al., Multiple conserved regulatory domains promote Fezf2 expression in the developing cerebral cortex William Harris. Neural Development (2014) doi:10.1186/1749-8104-9-6

Vitting-Seerup Kristoffer et al., spliceR: an R package for classification of alternative splicing and prediction of coding potential from RNA-seq data Transcriptome analysis. BMC Bioinformatics (2014) doi:10.1186/1471-2105-15-81

Tayebi Naeimeh et al., Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families. Orphanet Journal of Rare Diseases (2014) doi:10.1186/s13023-014-0108-6

More about the resource:

VISTA is a powerful comparative genomics system which may lead to discoveries of medical importance. The VISTA family of tools is developed and hosted at Genomics Division of Lawrence Berkeley National Laboratory. This collaborative effort is supported by supported by the Programs for Genomic Applications grant from the NHLBI/NIH and the Office of Biological and Environmental Research, Office of Science, US Department of Energy.


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The materials and slides offered can not be resold or used for profit purposes. Reproduction, distribution and/or use is strictly limited to instructional purposes only and can not be used for for monetary gain or wide distribution.
Copyright 2009, OpenHelix, LLC.

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