1-7 of 7
Authors: Alberto Magi
Journal Article
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing
Bioinformatics, Volume 36, Issue 4, February 2020, Pages 1267–1269, https://doi.org/10.1093/bioinformatics/btz719
Published: 07 October 2019
Journal Article
PyPore: a python toolbox for nanopore sequencing data handling
Bioinformatics, Volume 35, Issue 21, November 2019, Pages 4445–4447, https://doi.org/10.1093/bioinformatics/btz269
Published: 16 April 2019
Journal Article
Nano-GLADIATOR: real-time detection of copy number alterations from nanopore sequencing data
Bioinformatics, Volume 35, Issue 21, November 2019, Pages 4213–4221, https://doi.org/10.1093/bioinformatics/btz241
Published: 05 April 2019
Journal Article
H 3 M 2 : detection of runs of homozygosity from whole-exome sequencing data
Bioinformatics, Volume 30, Issue 20, October 2014, Pages 2852–2859, https://doi.org/10.1093/bioinformatics/btu401
Published: 24 June 2014
Journal Article
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript
Bioinformatics, Volume 28, Issue 24, December 2012, Pages 3232–3239, https://doi.org/10.1093/bioinformatics/bts617
Published: 23 October 2012
Journal Article
Read count approach for DNA copy number variants detection
Bioinformatics, Volume 28, Issue 4, February 2012, Pages 470–478, https://doi.org/10.1093/bioinformatics/btr707
Published: 23 December 2011
Journal Article
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data
Bioinformatics, Volume 22, Issue 1, January 2006, Pages 50–57, https://doi.org/10.1093/bioinformatics/bti750
Published: 02 November 2005
