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Maarja Lepamets

Showing results (1-10 of 16) with videos related to

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Gigascience|December 8, 2015
GenomeTester4: a toolkit for performing basic set operations - union, intersection and complement on k-mer listsLauris Kaplinski, Maarja Lepamets, Maido Remm
Nature Communications|June 19, 2021
Genome-wide association study identifies five risk loci for pernicious anemiaTriin Laisk, Maarja Lepamets, Mariann Koel, et al.
Bioinformatics (Oxford, England)|January 24, 2018
Primer3_masker: integrating masking of template sequence with primer design softwareTriinu Kõressaar, Maarja Lepamets, Lauris Kaplinski, 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.
BMC Cancer|June 12, 2019
Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratificationKristi Läll, Maarja Lepamets, Marili Palover, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 18, 2018
Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutionsSulev Reisberg, Kristi Krebs, Maarja Lepamets, et al.
American Journal of Human Genetics|March 3, 2022
The individual and global impact of copy-number variants on complex human traitsChiara Auwerx, Maarja Lepamets, Marie C Sadler, et al.
Peerj|May 24, 2017
StrainSeeker: fast identification of bacterial strains from raw sequencing reads using user-provided guide treesMärt Roosaare, Mihkel Vaher, Lauris Kaplinski, et al.
Nature Communications|June 23, 2022
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapseNatàlia Pujol-Gualdo, Kristi Läll, Maarja Lepamets, et al.
HGG Advances|August 29, 2022
Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associationsMaarja Lepamets, Chiara Auwerx, Margit Nõukas, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Gigascience|December 8, 2015
GenomeTester4: a toolkit for performing basic set operations - union, intersection and complement on k-mer listsLauris Kaplinski, Maarja Lepamets, Maido Remm
Nature Communications|June 19, 2021
Genome-wide association study identifies five risk loci for pernicious anemiaTriin Laisk, Maarja Lepamets, Mariann Koel, et al.
Bioinformatics (Oxford, England)|January 24, 2018
Primer3_masker: integrating masking of template sequence with primer design softwareTriinu Kõressaar, Maarja Lepamets, Lauris Kaplinski, 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.
BMC Cancer|June 12, 2019
Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratificationKristi Läll, Maarja Lepamets, Marili Palover, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 18, 2018
Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutionsSulev Reisberg, Kristi Krebs, Maarja Lepamets, et al.
American Journal of Human Genetics|March 3, 2022
The individual and global impact of copy-number variants on complex human traitsChiara Auwerx, Maarja Lepamets, Marie C Sadler, et al.
Peerj|May 24, 2017
StrainSeeker: fast identification of bacterial strains from raw sequencing reads using user-provided guide treesMärt Roosaare, Mihkel Vaher, Lauris Kaplinski, et al.
Nature Communications|June 23, 2022
Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapseNatàlia Pujol-Gualdo, Kristi Läll, Maarja Lepamets, et al.
HGG Advances|August 29, 2022
Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associationsMaarja Lepamets, Chiara Auwerx, Margit Nõukas, et al.
Pageof 2