Difference between revisions of "RTG"

From SEQwiki
Jump to: navigation, search
(Created page with "{{Bioinformatics application |sw summary=Unique mapping speed and sensitivity delivers to genome center standards through easy-to-operate variant detection and metagenomic analys...")
 
(Description)
Line 14: Line 14:
 
== Description ==
 
== Description ==
 
<!-- Describe the application in the space below -->  
 
<!-- Describe the application in the space below -->  
RTG Investigator is easy-to-operate sequence analysis software that delivers to genome center standards.  Unparalleled mapping speed and sensitivity powers comprehensive variant detection and metagenomic analysis pipelines that support integrate Illumina, Complete Genomics and Roche 454 data sets.  The software is available free for individual use.   
+
RTG Investigator is easy-to-operate sequence analysis software that delivers to genome center standards.  Unparalleled mapping speed and sensitivity powers comprehensive variant detection and metagenomic analysis pipelines that support Illumina, Complete Genomics and Roche 454 data sets.  The software is available free for individual use.   
  
  

Revision as of 07:40, 21 June 2011

Application data

Biological application domain(s) Exome and Whole genome variant detection, Metagenomics
Principal bioinformatics method(s) Mapping, Alignment, SNP/Indel calling, Translated nucleotide search, K-mer analysis, Species frequency estimation, Contaminant filtering
Technology Illumina, Complete Genomics, Roche 454
Created at Real Time Genomics, Inc.
Maintained? Yes
Input format(s) FASTA, FASTQ, Complete Genomics
Output format(s) SAM, BED, VCF
Licence Commercial software, free for individual use
Operating system(s) Linux, Mac OS X, Windows

Summary: Unique mapping speed and sensitivity delivers to genome center standards through easy-to-operate variant detection and metagenomic analysis pipelines. 200px|right

"Error: no local variable "counter" was set." is not a number.

Description

RTG Investigator is easy-to-operate sequence analysis software that delivers to genome center standards. Unparalleled mapping speed and sensitivity powers comprehensive variant detection and metagenomic analysis pipelines that support Illumina, Complete Genomics and Roche 454 data sets. The software is available free for individual use.






Links


References

  1. . 2014. Journal of Computational Biology


To add a reference for RTG, enter the PubMed ID in the field below and click 'Add'.

 


Search for "RTG" in the SEQanswers forum / BioStar or:

Web Search Wiki Sites Scientific