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Year | Number of Results |
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2017 | 1 |
2019 | 1 |
2021 | 1 |
2023 | 3 |
2024 | 0 |
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Page 1
Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection.
medRxiv [Preprint]. 2023 Jan 31:2023.01.28.23285140. doi: 10.1101/2023.01.28.23285140.
medRxiv. 2023.
PMID: 36778285
Free PMC article.
Preprint.
GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing reads.
Pajuste FD, Remm M.
Pajuste FD, et al.
Sci Rep. 2023 Oct 18;13(1):17765. doi: 10.1038/s41598-023-44636-z.
Sci Rep. 2023.
PMID: 37853040
Free PMC article.
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KATK: Fast genotyping of rare variants directly from unmapped sequencing reads.
Kaplinski L, Möls M, Puurand T, Pajuste FD, Remm M.
Kaplinski L, et al. Among authors: pajuste fd.
Hum Mutat. 2021 Jun;42(6):777-786. doi: 10.1002/humu.24197. Epub 2021 Apr 1.
Hum Mutat. 2021.
PMID: 33715282
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Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events.
Heyne HO, Pajuste FD, Wanner J, Onwuchekwa JID, Mägi R, Palotie A; FinnGen, Estonian Biobank research team; Kälviainen R, Daly MJ.
Heyne HO, et al. Among authors: pajuste fd.
medRxiv [Preprint]. 2023 Nov 27:2023.11.27.23297542. doi: 10.1101/2023.11.27.23297542.
medRxiv. 2023.
PMID: 38076931
Free PMC article.
Preprint.
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AluMine: alignment-free method for the discovery of polymorphic Alu element insertions.
Puurand T, Kukuškina V, Pajuste FD, Remm M.
Puurand T, et al. Among authors: pajuste fd.
Mob DNA. 2019 Jul 18;10:31. doi: 10.1186/s13100-019-0174-3. eCollection 2019.
Mob DNA. 2019.
PMID: 31360240
Free PMC article.
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FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads.
Pajuste FD, Kaplinski L, Möls M, Puurand T, Lepamets M, Remm M.
Pajuste FD, et al.
Sci Rep. 2017 May 31;7(1):2537. doi: 10.1038/s41598-017-02487-5.
Sci Rep. 2017.
PMID: 28566690
Free PMC article.
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