Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Märt Möls"'
Autor:
Maris Alver, Silva Kasela, Liina Haring, Laura Birgit Luitva, Krista Fischer, Märt Möls, Lili Milani
Publikováno v:
The Lancet Regional Health. Europe, Vol 41, Iss , Pp 100914- (2024)
Summary: Background: Schizophrenia (SCZ) patients exhibit 30% higher prevalence of metabolic syndrome (MetS) compared to the general population with its suboptimal management contributing to increased mortality. Large-scale studies providing real-wor
Externí odkaz:
https://doaj.org/article/4c2ab3b3f7a94a85b5939440c306859a
Publikováno v:
PLoS Genetics, Vol 16, Iss 8, p e1008981 (2020)
Tribbles homolog 3 (TRIB3) is pseudokinase involved in intracellular regulatory processes and has been implicated in several diseases. In this article, we report that human TRIB3 promoter contains a 33-bp variable number tandem repeat (VNTR) and char
Externí odkaz:
https://doaj.org/article/a243553c8728466980fe2bfd11427ed8
Autor:
Fanny-Dhelia Pajuste, Lauris Kaplinski, Märt Möls, Tarmo Puurand, Maarja Lepamets, Maido Remm
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract We have developed a computational method that counts the frequencies of unique k-mers in FASTQ-formatted genome data and uses this information to infer the genotypes of known variants. FastGT can detect the variants in a 30x genome in less t
Externí odkaz:
https://doaj.org/article/e60e1692858c4df3bb8f5736e3177bde
Publikováno v:
PeerJ, Vol 6, p e4588 (2018)
Background Plasmids play an important role in the dissemination of antibiotic resistance, making their detection an important task. Using whole genome sequencing (WGS), it is possible to capture both bacterial and plasmid sequence data, but short rea
Externí odkaz:
https://doaj.org/article/81102ee9fd5248faa59effa0760bc0ab
Autor:
Märt Roosaare, Mihkel Vaher, Lauris Kaplinski, Märt Möls, Reidar Andreson, Maarja Lepamets, Triinu Kõressaar, Paul Naaber, Siiri Kõljalg, Maido Remm
Publikováno v:
PeerJ, Vol 5, p e3353 (2017)
Background Fast, accurate and high-throughput identification of bacterial isolates is in great demand. The present work was conducted to investigate the possibility of identifying isolates from unassembled next-generation sequencing reads using custo
Externí odkaz:
https://doaj.org/article/6b879052f9ac47628d2791bf918f1fd3
Autor:
Alena Kushniarevich, Olga Utevska, Marina Chuhryaeva, Anastasia Agdzhoyan, Khadizhat Dibirova, Ingrida Uktveryte, Märt Möls, Lejla Mulahasanovic, Andrey Pshenichnov, Svetlana Frolova, Andrey Shanko, Ene Metspalu, Maere Reidla, Kristiina Tambets, Erika Tamm, Sergey Koshel, Valery Zaporozhchenko, Lubov Atramentova, Vaidutis Kučinskas, Oleg Davydenko, Olga Goncharova, Irina Evseeva, Michail Churnosov, Elvira Pocheshchova, Bayazit Yunusbayev, Elza Khusnutdinova, Damir Marjanović, Pavao Rudan, Siiri Rootsi, Nick Yankovsky, Phillip Endicott, Alexei Kassian, Anna Dybo, Genographic Consortium, Chris Tyler-Smith, Elena Balanovska, Mait Metspalu, Toomas Kivisild, Richard Villems, Oleg Balanovsky
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0135820 (2015)
The Slavic branch of the Balto-Slavic sub-family of Indo-European languages underwent rapid divergence as a result of the spatial expansion of its speakers from Central-East Europe, in early medieval times. This expansion-mainly to East Europe and th
Externí odkaz:
https://doaj.org/article/bce78ff47b974aa1809f3a1e09f56a8d
Autor:
Priit Palta, Lauris Kaplinski, Liina Nagirnaja, Andres Veidenberg, Märt Möls, Mari Nelis, Tõnu Esko, Andres Metspalu, Maris Laan, Maido Remm
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0122713 (2015)
DNA copy number variants (CNVs) that alter the copy number of a particular DNA segment in the genome play an important role in human phenotypic variability and disease susceptibility. A number of CNVs overlapping with genes have been shown to confer
Externí odkaz:
https://doaj.org/article/464c8e0d297544dd8f1251794e559aef
Autor:
Chandana Basu Mallick, Florin Mircea Iliescu, Märt Möls, Sarah Hill, Rakesh Tamang, Gyaneshwer Chaubey, Rie Goto, Simon Y W Ho, Irene Gallego Romero, Federica Crivellaro, Georgi Hudjashov, Niraj Rai, Mait Metspalu, C G Nicholas Mascie-Taylor, Ramasamy Pitchappan, Lalji Singh, Marta Mirazon-Lahr, Kumarasamy Thangaraj, Richard Villems, Toomas Kivisild
Publikováno v:
PLoS Genetics, Vol 9, Iss 11, p e1003912 (2013)
Skin pigmentation is one of the most variable phenotypic traits in humans. A non-synonymous substitution (rs1426654) in the third exon of SLC24A5 accounts for lighter skin in Europeans but not in East Asians. A previous genome-wide association study
Externí odkaz:
https://doaj.org/article/b8f512c6a2614cb2a0b6dc45e50b9150
Publikováno v:
Human Mutation. 42:777-786
MotivationKATK is a fast and accurate software tool for calling variants directly from raw NGS reads. It uses predefined k-mers to retrieve only the reads of interest from the FASTQ file and calls genotypes by aligning retrieved reads locally. KATK d
Autor:
Andres Kiviste, Toivo Vajakas, Märt Möls, Mati Tee, Allan Sims, Kalev Pärna, Mattias Rennel, Raul Kangro, Marta Mõistus, Mait Lang
Publikováno v:
Forestry Studies. 73:77-97
Since 1999, Estonia has conducted the National Forest Inventory (NFI) on the basis of sample plots. This paper presents a new module, incorporating remote-sensing feature variables from airborne laser scanning (ALS) and from multispectral satellite i