SPiCE is no longer maintained. To access the tool's predictions, please use SPiP, accessible at : https://sourceforge.net/projects/splicing-prediction-pipeline/ or https://github.com/raphaelleman/SPiP
If you have questions, please contact me to: r.leman@baclesse.unicancer.fr or raphael.leman@orange.fr
v2.1.5 (05/2019) + corr (01/2020):
Fix bug for linux version
v2.1.4 (03/2019):
Proxy management (only for Windows version)
v2.1.3 (07/2018):
correction bug for first 3' ss
import...
PySCeS CBMPy is a new platform for constraint based modelling and analysis. It has been designed using principles developed in the PySCeS simulation software project: usability, flexibility and accessibility.
CBMPy supports the latest standards for encoding CBM models encoding, SBML L3 FBC, COBRA as well as MIRIAM compliant RDF and custom annotations.
Its architecture is both extensible and flexible using data structures that are intuitive to the biologist while transparently...
DAWGPAWS is a suite of command line programs written in Perl that accelerates annotation of genes and transposable elements in plant genomes by automating the process of running annotation programs and facilitating combined evidence annotation curation.
Auth0 Token Vault handles secure token storage, exchange, and refresh for external providers so you don't have to build it yourself.
Rolling your own OAuth token storage can be a security liability. Token Vault securely stores access and refresh tokens from federated providers and handles exchange and renewal automatically. Connected accounts, refresh exchange, and privileged worker flows included.
parFE is fully-parallel high-performance finite element code targeted to the modeling of trabecular bones in humans. It employs scalable multigrid solvers for efficient solutions on massively parallel computers.
FieldML consists of a serialisation format and an API and an implementation of the API. It focuses on representing finite element meshes, and fields on meshes. Based on the already successful format used by CMISS (www.cmiss.org)
ReAlignerV is an alignment tool focusing on genomic nucleotide
sequences upstream of genes. ReAlignerV integrates TRANSFAC(R) Match(TM)
results to detect the conserved TFBSs.
ReAlignerV is robust against transposable element insertions.