Software

Software related to the project, developped within the Alcovna/Colib’read projects, or not.

  • KisSplice – A local transcriptome assembler for SNPs, indels and AS events
  • Mapsembler2 – targeted assembly and visualization
  • discoSnp++ – discovering Single Nucleotide Polymorphism (SNP) from raw set(s) of reads
  • TakeABreak – inversion breakpoints detection directly from raw NGS reads
  • Lordec – hybrid error correction program for long, PacBio reads
  • Commet – comparing and combining multiple metagenomic datasets
  • Short Read Connector – connect reads from (meta)-genomic dataset(s)
  • MindTheGap – detection and assembly of DNA insertion variants in NGS read datasets with respect to a reference genome
  • Leon – reference-free read compression
  • Minia – short-read assembler based on a de Bruijn graph

discoSnp++

[page edited on June, 18, 2020] – github webpage Tutorial A toturial can be followed from those slides demo_discosnp Description Software discoSnp++ is designed for discovering Single Nucleotide Polymorphism (SNP) and insertions/deletions (indels) from raw set(s) of reads obtained with Next Generation Sequencers (NGS). Note that number of input read sets is not constrained, it can …

TakeABreak

[last edited on July, 7, 2015] Description TakeABreak is a tool that can detect inversion breakpoints directly from raw NGS reads, without the need of any reference genome and without de novo assembling the genomes. Its implementation has a very limited memory impact allowing its usage on common desktop computers and acceptable runtime (Illumina reads …

Commet

Comparing and combining multiple metagenomic datasets [PAGE Created on July, 29 2014] Description: COMMET (“COmpare Multiple METagenomes”) provides a global similarity overview between all datasets of a large metagenomic project. Directly from non-assembled reads, all against all comparisons are performed through an efficient indexing strategy. Then, results are stored as bit vectors, a compressed representation …

Compareads

Compareads is no more maintained. You can now use the new Commet software which does more and better than compareads. [PAGE UPDATED on July, 29 2014] Description: Compareads is a tool designed to extract similar reads between potentially huge metagenomic datasets (i.e., hundreds of millions reads per dataset) Download: The last Compareads release may be …

Crac

See here: http://crac.gforge.inria.fr/

Gk-Arrays

See here: http://crac.gforge.inria.fr/gkarrays/

Kissplice

See here: http://kissplice.prabi.fr/

MindTheGap

MindTheGap is a tool to detect and assemble insertion variants of any size and any type, by comparison with a reference genome. For download and more details, see the web page : https://gatb.inria.fr/software/mind-the-gap/ Citation Guillaume Rizk, Anaïs Gouin, Rayan Chikhi and Claire Lemaitre. MindTheGap : integrated detection and assembly of short and long insertions. Bioinformatics …

Minia

See here: http://minia.genouest.org/

Mapsembler2

[page edited on August, 24th, 2020] Mapsembler2 is not maintained anymore Sadly, we have no more man power to maintain and to update Mapsembler2.  The last (2014) version is this one:  mapsembler2_2.2.4. Many bug fixes, new features, and optimizations are expected. Any help would be warmly welcome! Mapsembler2 description and possible usages: Mapsembler2 is a …

ANR Colib'read
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.