2020
DOI: 10.1016/j.dib.2020.105710
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Data on genetic polymorphism of flax (Linum usitatissimum L.) pathogenic fungi of Fusarium, Colletotrichum, Aureobasidium, Septoria, and Melampsora genera

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Cited by 16 publications
(12 citation statements)
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“…This knowledge is useful for phylogenetic studies and species resolution [ 14 , 15 ]. For initial identification, fungal barcodes can be used, e.g., the beta-tubulin ( TUB2 ) gene or the ITS region [ 16 , 17 , 18 , 19 ]. However, molecular markers sometimes provide limited information on species.…”
Section: Introductionmentioning
confidence: 99%
“…This knowledge is useful for phylogenetic studies and species resolution [ 14 , 15 ]. For initial identification, fungal barcodes can be used, e.g., the beta-tubulin ( TUB2 ) gene or the ITS region [ 16 , 17 , 18 , 19 ]. However, molecular markers sometimes provide limited information on species.…”
Section: Introductionmentioning
confidence: 99%
“…This approach significantly reduces the cost of sequencing per genotype compared to the whole genome analysis and allows the sequencing of dozens and hundreds of genome regions in hundreds and thousands of samples. It also overcomes the difficulties of Sanger sequencing associated with polyploidy of plant genomes and a high degree of duplication of their genes [ 18 , 97 , 98 , 99 , 100 , 101 ]. Therefore, the third approach, developed by us, for the identification of the three low-LIN mutations in the FAD3A and FAD3B genes in flax genotypes was based on targeted deep sequencing.…”
Section: Discussionmentioning
confidence: 99%
“…One microgram of RNA for each sample was treated with DNase I (Thermo Fisher Scientific, Waltham, MA, United States) and used for reverse transcription with random hexamer primers (Evrogen, Moscow, Russia) and Mint reverse transcriptase (Evrogen) following the manufacturer's protocol. Primers were designed for amplification of parts of the TCP, CLC, and MET1 genes and further sequencing on the Illumina platform as described in our previous works (Melnikova et al, 2019;Dmitriev et al, 2020;Novakovskiy et al, 2020). In brief, two PCRs were used for the library preparation.…”
Section: Targeted Genome and Transcriptome Sequencingmentioning
confidence: 99%