GENALICE MAP
|
Application data |
|
| Biological application domain(s) | Genomics |
|---|---|
| Principal bioinformatics method(s) | Read mapping, Variant calling |
| Technology | Illumina HiSeq X Ten |
| Created at | GENALICE B.V. |
| Maintained? | Yes |
| Input format(s) | FASTQ |
| Output format(s) | GAR, BAM, VCF |
| Software features | ultrafast alignment and variant calling |
| Licence | Commercial |
| Operating system(s) | Linux |
| Contact: | info@genalice.com |
Summary: From FASTQ to VCF in 30 min or less. Ultra-fast Next-Generation Sequencing (NGS) read alignment and variant calling solution.
"Error: no local variable "counter" was set." is not a number.
Description
For NGS short read alignment speed, accuracy, flexibility and storage footprint reduction of preprocessed NGS data are the key challenges.
GENALICE MAP is a Next-Generation alignment solution that deals with all. GENALICE MAP preprocesses your data on standard dual processor hardware. Faster, better and extremely cost-effective.
Links
References
none specified
To add a reference for GENALICE MAP, enter the PubMed ID in the field below and click 'Add'.
[ edit box ]
Search for "GENALICE MAP" in the SEQanswers forum / BioStar or:
| Web Search | Wiki Sites | Scientific |
|---|---|---|
