Valtteri Wirta

According to our database, Valtteri Wirta authored at least 4 papers between 2020 and 2026.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2026

Nallo: a Nextflow pipeline for comprehensive human long-read genome analysis.

Felix Lenner, Anders Jemt, Lucia Peña Pérez, Ramprasad Neethiraj, Peter Pruisscher, Daniel Schmitz, Annick Renevey, Pádraic Corcoran, Daniel Nilsson, Jesper Eisfeldt, Anna Lindstrand, Valtteri Wirta, Adam Ameur, Lars Feuk

Bioinform., 2026

2024

Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysis.

Orlinda Brahimllari, Sandra Eloranta, Patrik Georgii-Hemming, Zahra Haider, Sabine Koch, Aleksandra Krstic, Frantzeska Papadopoulou Skarp, Richard Rosenquist, Karin E. Smedby, Fulya Taylan, Birna Thorvaldsdottir, Valtteri Wirta, Tove Wästerlid, Magnus Boman

Health Informatics J., 2024

2020

Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants.

Maxime Garcia, Szilveszter Juhos, Malin Larsson, Páll Ísólfur Ólason, Marcel Martin, Jesper Eisfeldt, Sebastian DiLorenzo, Johanna Sandgren, Teresita Diaz de Ståhl, Philip Ewels, Valtteri Wirta, Monica Nistér, Max Käller, Björn Nystedt

F1000Research, 2020

Loqusdb: added value of an observations database of local genomic variation.

Måns Magnusson, Jesper Eisfeldt, Daniel Nilsson, Adam Rosenbaum, Valtteri Wirta, Anna Lindstrand, Anna Wedell, Henrik Stranneheim

BMC Bioinform., 2020