Difference between revisions of "Services"

From Bioinformatics Core Wiki
(Data analysis)
(Basic services)
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== Basic services ==
 
== Basic services ==
  
·      Consultation on bioinformatics methods and resources
+
* Consultation on bioinformatics methods and resources
 
+
* Software evaluation, implementation, and training
·      Software evaluation, implementation, and training
+
* Customization of bioinformatics resources
 
+
* Training on different bioinformatics topics
·      Customization of bioinformatics resources
+
 
+
·      Training on different bioinformatics topics
+
  
 
== Advanced services ==
 
== Advanced services ==

Revision as of 18:05, 30 October 2012

We currently offer different types of services for internal and external users:

Basic services

  • Consultation on bioinformatics methods and resources
  • Software evaluation, implementation, and training
  • Customization of bioinformatics resources
  • Training on different bioinformatics topics

Advanced services

Data analysis

  • High-throughput data analysis of genomics, transcriptomics, epigenetics and proteomics datasets
  • Next-Gen data analysis. The unit has invested time and effort in establishing several pipelines dedicated to the analysis of Deep-sequencing data. Currently, the unit has experience analyzing different types of deep-sequencing data:
1) ChIP-Seq
· Transcription factor binding site detection / motif discovery
· Analysis of histone modifications
· Identification of target genes
· Data Visualization
2) High-resolution nucleosome positioning
3) Detection of Chromosomal Interactions (5C)
4) RNA-Seq
· Differential expression at the gene and transcript level
· Detection of rare, or novel transcripts
· Identification of alternative splicing and report of isoform abundance
· microRNA / Small RNA analysis (profiling and discovery)
· De-novo transcriptome assembly
· Data visualization
5) Variation Detection
· SNP calling
· Indel calling
· Variation filtration
· Functional impact assessment
· Data visualization
6) De novo genome assembly
· Downstream analysis for the interpretation of gene lists, including gene set enrichment, GO and pathway analysis, orthology prediction
  • Identification of functional elements in the genomes:
    • Automatic gene annotation (including non-coding genes)
    • Regulatory sequences: DNA motif analysis (novel and known)
  • Evolution of proteins:
    • Multiple Sequence Alignments
    • Orthology assignments
    • Protein structure comparisons
    • Fold Recognition
    • Phylogenetic analysis

Software Development and Data Management

  • Database design and development
  • Web interface development
  • Development of versatile ticketing and project management systems based on wiki technologies
  • Implementation of integrative bioinformatics web applications
  • Implementation of customized Genome browsers
  • Support for submission of raw data to public repositories (ENA, SRA, GEO..)
Bioinformatics Core Facility @ CRG — 2011-2024