BLISS statistics

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

Subscribe
info

Citations per year

Citations chart
info

Popular tool citations

chevron_left Cis-regulatory module prediction chevron_right
Popular tools chart
info

Tool usage distribution map

Tool usage distribution map
info

Associated diseases

Associated diseases

BLISS specifications

Information


Unique identifier OMICS_10964
Name BLISS
Interface Web user interface
Restrictions to use None
Input data Given two orthologous DNA sequences, BLISS 2.0 is able to output all constrained clusters shared by those two sequences.
Computer skills Basic
Version 2.0
Stability No
Maintained No

Publications for BLISS

BLISS in publication

PMCID: 2669485
PMID: 19284541
DOI: 10.1186/1471-2105-10-82

[…] of tissue-specific approaches., there are two published methods proposing computational prediction of crms based on a non-specific motif set. though we could not compare our results with the bliss algorithm [], as it seems to be limited to sequences significantly smaller than 15000 bp. we believe that this is due to the fact, that the computation cost was too high. actually, the time […]


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

BLISS institution(s)
Department of Computer and Information Science and Engineering, College of Engineering, UFL, Gainesville, FL, USA; Department of Molecular Genetics and Microbiology & UF Shands Cancer Center, College of Medicine, UFL, Gainesville, FL, USA
BLISS funding source(s)
This work was supported in part by a UF Genetic Institute Seed Grant and by NIH CA095542 and AI067555.

BLISS reviews

star_border star_border star_border star_border star_border
star star star star star

Be the first to review BLISS