Aligning short reads to reference alignments and trees
By Simon A. Berger, Alexandros Stamatakis. 2011
193 citations recorded by the source corpus.
Subfields: Cancer Research, Information Systems and Management, Molecular Biology
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Kazutaka Katoh
- Daron M. Standley
- Jeremy D. Buhler
- Hongtao Sun
- Nick Goldman
- Ari Löytynoja
- Albert J. Vilella
- W. Garrett
In Information Systems and Management
- Kazutaka Katoh
- Daron M. Standley
- Jeremy D. Buhler
- Hongtao Sun
- Nick Goldman
- Ari Löytynoja
- Albert J. Vilella
- Curtis Huttenhower
In Molecular Biology
- Kazutaka Katoh
- Daron M. Standley
- Curtis Huttenhower
- Nicola Segata
- Ari Löytynoja
- Alexandros Stamatakis
- Xochitl C. Morgan
- Nick Goldman
Citations in the corpus
- MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability (2013, methodology): “Several tools (Berger and Stamatakis 2011; Löytynoja et al. 2012; Sun and Buhler 2012) for this purpose were developed between 2011 and 2012.”
- PhyLAT: a phylogenetic local alignment tool (2012, methodology): “PaPaRa (Berger and Stamatakis, 2011), unlike the tools described above, uses a guide tree to map queries, in particular short reads, to an existing multiple alignment, but it does not score or improve the resulting alignments probabilistically given the phylogeny.”
- Computational meta'omics for microbial community studies (2013, methodology): “(MEGAN (Huson et al, 2007)) or other parsimonious evolutionary principles (PaPaRa (Berger and Stamatakis, 2011)).”
- EPA-ng: Massively Parallel Evolutionary Placement of Genetic Sequences (2018, methodology): “It effectively strips the input Multiple Sequence Alignments (MSAs) of all sites that are unlikely to contribute substantially to the placement likelihood score.”
- Accurate extension of multiple sequence alignments using a phylogeny-aware graph algorithm (2012, methodology): “The methods tested for both were PAGAN/guided, PAGAN/free (v.0.33), hmmalign (from the HMMER package, v.3.0; Eddy, 2011), MAFFT (v.6.860b; Katoh et al., 2002) and ClustalW (v.2.1; Larkin et al., 2007); for DNA we also used PaPaRa (RAxML v.7.2.6; Berger and 1687 [16:07 19/6/2012 Bioinformatics-bts198”