galign statistics

To access cutting-edge analytics on consensus tools, life science contexts and associated fields, you will need to subscribe to our premium service.


Citations per year

Citations chart

Popular tool citations

chevron_left Read alignment SNP detection chevron_right
Popular tools chart

Tool usage distribution map

Tool usage distribution map

Associated diseases

Associated diseases

galign specifications


Unique identifier OMICS_24204
Name galign
Software type Application/Script
Interface Command line interface
Restrictions to use None
Operating system Mac OS
Programming languages C++
Computer skills Advanced
Version 1.0
Stability Stable
Source code URL
Maintained Yes



Add your version


  • person_outline Shai Shaham <>

Publication for galign

galign in publication

PMCID: 5084644
PMID: 27810909
DOI: 10.1083/jcb.201601083

[…] using the solexa genome analyzer (illumina) 36-bp single-end reads were obtained at 13× coverage of the c. elegans genome. we used three programs to analyze the sequence reads. maqgene, maq, and galign programs were individually used to align the sequence reads to the c. elegans genome and annotate snps (; ; ). we also aligned the sequence reads to the genome with the program bowtie, […]

To access a full list of publications, you will need to upgrade to our premium service.

galign institution(s)
Laboratory of Developmental Genetics, The Rockefeller University, New York, NY, USA
galign funding source(s)
Supported in part by NIH grants R01 HD042680, R01 NS064273, and R01 HD052677.

galign reviews

star_border star_border star_border star_border star_border
star star star star star

Be the first to review galign