ASTALAVISTA |
Detect alternative splicing events |
http://astalavista.sammeth.net/ |
Foissac and Sammeth,2007 |
CASH |
Detect alternative splicing events |
https://sourceforge.net/projects/cash-program/ |
Wu et al.,2018 |
CodingQuarry |
Gene prediction (HMM-based) using both RNA-Seq data and genome sequence |
https://sourceforge.net/projects/codingquarry/ |
Testa et al.,2015 |
GMAP |
Spliced alignment to genome |
http://research-pub.gene.com/gmap/ |
Wu and Watanabe,2005 |
LoRDEC |
Error correction of FLNC with short read RNA-seq |
http://atgc.lirmm.fr/lordec |
Salmela and Rivals,2014 |
LoReAn |
Comparative analysis and annotation: identify novel isoforms/genes against reference annotation |
https://github.com/lfaino/LoReAn |
Cook et al.,2018 |
LSC |
Error correction of FLNC with short read RNA-seq |
http://augroup.org/LSC/LSC_download.html |
Au et al.,2012 |
minimap2 |
Spliced alignment to genome |
https://github.com/lh3/minimap2 |
Li,2018 |
PASA |
Detect alternative splicing events |
https://pasapipeline.github.io/ |
Liu et al.,2017 |
Proovread |
Error correction of FLNC with short read RNA-seq |
https://github.com/BioInf-Wuerzburg/proovread |
Hackl et al.,2014 |
Quiver |
Polishing PacBio RS II reads |
https://github.com/PacificBiosciences/ GenomicConsensus |
Chin et al.,2013 |
SpliceGrapher |
Detect alternative splicing events |
http://splicegrapher.sourceforge.net/ |
Rogers et al.,2012 |
SQANTI |
Comparative analysis and annotation: identify novel isoforms/genes against reference annotation |
https://bitbucket.org/ConesaLab/sqanti |
Tardaguila et al.,2018 |
STAR |
Spliced alignment to genome |
https://github.com/alexdobin/STAR/releases |
Dobin et al.,2013 |
SUPPA |
Detect alternative Splicing events |
https://bitbucket.org/regulatorygenomicsupf/suppa |
Alamancos et al.,2015 |
TAPIS |
Alternative splicing, collapsing redundant or degraded transcripts |
https://bitbucket.org/comp_bio/tapis |
Abdel-Ghany et al.,2016 |
ToFU |
Preprocessing (collapse to non-redundant isoforms) |
https://github.com/PacificBiosciences/IsoSeq_SA3nUP |
Gordon et al.,2015 |