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Nucleic Acids Research|July 18, 2006
SNPmasker: automatic masking of SNPs and repeats across eukaryotic genomesReidar Andreson, Tarmo Puurand, Maido Remm
Bioinformatics (Oxford, England)|December 16, 2004
MultiPLX: automatic grouping and evaluation of PCR primersLauris Kaplinski, Reidar Andreson, Tarmo Puurand, et al.
Bioinformatics Advances|August 29, 2023
DOCEST-fast and accurate estimator of human NGS sequencing depth and error rateLauris Kaplinski, Märt Möls, Tarmo Puurand, et al.
Mobile DNA|July 31, 2019
AluMine: alignment-free method for the discovery of polymorphic Alu element insertionsTarmo Puurand, Viktoria Kukuškina, Fanny-Dhelia Pajuste, et al.
Human Mutation|March 14, 2021
KATK: Fast genotyping of rare variants directly from unmapped sequencing readsLauris Kaplinski, Märt Möls, Tarmo Puurand, et al.
Scientific Reports|June 2, 2017
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing readsFanny-Dhelia Pajuste, Lauris Kaplinski, Märt Möls, et al.
Plos Genetics|August 4, 2020
A human-specific VNTR in the TRIB3 promoter causes gene expression variation between individualsTiit Örd, Tarmo Puurand, Daima Örd, et al.
Genome Biology|August 13, 2025
Y-mer: a k-mer based method for determining human Y chromosome haplogroups from ultra-low sequencing depth dataTarmo Puurand, Märt Möls, Lauris Kaplinski, et al.
European Journal of Human Genetics : EJHG|November 14, 2018
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health recordsTõnis Tasa, Kristi Krebs, Mart Kals, et al.
Nature|July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.
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