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Bioinformatics Advances|March 11, 2024
Tackling reference bias in genotyping by using founder sequences with PanVC 3Tuukka Norri, Veli MäkinenBriefings in Bioinformatics|January 11, 2017
Evaluating approaches to find exon chains based on long readsAnna Kuosmanen, Tuukka Norri, Veli MäkinenAlgorithms for Molecular Biology : AMB|May 28, 2019
Linear time minimum segmentation enables scalable founder reconstructionTuukka Norri, Bastien Cazaux, Dmitry Kosolobov, et al.Bioinformatics (Oxford, England)|July 14, 2021
Founder reconstruction enables scalable and seamless pangenomic analysisTuukka Norri, Bastien Cazaux, Saska Dönges, et al.BMC Genomics|May 17, 2018
Towards pan-genome read alignment to improve variation callingDaniel Valenzuela, Tuukka Norri, Niko Välimäki, et al.BMC Genomics|January 10, 2015
Recombination-aware alignment of diploid individualsVeli Mäkinen, Daniel ValenzuelaBioinformatics (Oxford, England)|July 24, 2021
Accurate spliced alignment of long RNA sequencing readsKristoffer Sahlin, Veli MäkinenBMC Bioinformatics|February 26, 2014
Haploid to diploid alignment for variation calling assessmentVeli Mäkinen, Jani RahkolaBMC Bioinformatics|October 4, 2012
Normalized N50 assembly metric using gap-restricted co-linear chainingVeli Mäkinen, Leena Salmela, Johannes YlinenPageof 4