2012
DOI: 10.1007/s00253-012-4228-4
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Genetic linkage mapping in fungi: current state, applications, and future trends

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Cited by 40 publications
(27 citation statements)
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“…For fundamental and applied interest, the dissection of genetic architecture of mycelium growth has been carried out in edible mushrooms using QTL mapping or other methodologies (Larraya et al 2001(Larraya et al , 2002Foulongne-Oriol 2012;Sivolapova et al 2012). In this study, we used three different segregation populations to uncover the loci regulating and controlling the vegetative mycelium growth rate of L. edodes.…”
Section: Qtls Controlling the Vegetative Mycelium Growth Ratementioning
confidence: 99%
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“…For fundamental and applied interest, the dissection of genetic architecture of mycelium growth has been carried out in edible mushrooms using QTL mapping or other methodologies (Larraya et al 2001(Larraya et al , 2002Foulongne-Oriol 2012;Sivolapova et al 2012). In this study, we used three different segregation populations to uncover the loci regulating and controlling the vegetative mycelium growth rate of L. edodes.…”
Section: Qtls Controlling the Vegetative Mycelium Growth Ratementioning
confidence: 99%
“…PCR-based AFLP markers have been widely used for their relatively high reproducibility and efficiency (Foulongne-Oriol 2012). Sequencerelated amplified polymorphism (SRAP) (Li & Quiros 2001) generates PCR-based markers targeting open reading frames (ORFs).…”
Section: Introductionmentioning
confidence: 99%
“…As for other crops, the type of genetic markers has developed from isozyme up to the now common single nucleotide polymorphic markers (SNPs; for an overview on markers used in linkage analysis in fungi, including A. bisporus see: Foulongne-Oriol 2012). May and Royse (1981, 1982) started to use isoenzyme markers to elucidate the life cycle of A. bisporus and confirm crosses between homokaryons.…”
Section: Genetic Markers and Genetic Dissection Of Traitsmentioning
confidence: 99%
“…As in plants, fungal lines with contrasting performance are commonly crossed to generate segregating populations and used to map genomic regions involved in traits and to identify candidate genes (Foulongne-Oriol 2012). This is usually done by protoplasting the heterokaryotic parental lines and recovering the constituent nuclei as homokaryons which are subsequently used for outcrossing.…”
Section: Introductionmentioning
confidence: 99%