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共检索到127条 ,权限内显示50条;
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Data from: Identification of multiple QTL hotspots in sockeye salmon (Oncorhynchus nerka) using genotyping-by-sequencing and a dense linkage map
- 负责人:
- DOI:
- doi:10.5061/dryad.5n0v4
- 摘要:
- in local adaptation and speciation. Here, we used genotyping-by-sequencing and a combination of previously published and newly generated data to construct sex-speci
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Identification of a dominant chlorosis phenotype through a forward screen of the Triticum turgidum cv. Kronos TILLING population
- 负责人:
- Uauy, Cristobal
- 关键词:
- durum wheat genomics senescence chlorosis bulked-segregant analysis TILLING mapping-by-sequencing
- DOI:
- doi:10.5061/dryad.g3r3hp7
- 摘要:
- , CA (US). To obtain further SNPs for fine-mapping, we isolated chromosome 3A using flow sorting and sequenced the entire chromosome. By mapping these reads ag
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Sequencing for SNP Discovery in Two Populations of Bighorn Sheep (Ovis canadensis)" in Genomic Resources Notes accepted 1 April 2013" data-category="" data-cropid="" data-dimen="" data-id="b378718b-f979-11ea-ae96-0242ac110002"> Data from: "RAD Sequencing for SNP Discovery in Two Populations of Bighorn Sheep (Ovis canadensis)" in Genomic Resources Notes accepted 1 April 2013
- 负责人:
- DOI:
- doi:10.5061/dryad.4qk81
- 摘要:
- low for fine-mapping of loci associated with horn size, and examination of the consequences of the genetic rescue including mapping genes underling differenc
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Utility of pooled sequencing for association mapping in non-model organisms
- 负责人:
- DOI:
- doi:10.5061/dryad.85q6j
- 摘要:
- for association mapping in model organisms, it has not been frequently utilized in natural populations. To extend bioinformatic tools for rapid implementation of Pool-Se
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: QTL analysis of soft scald in two apple populations
- 负责人:
- Myles, Sean
- 关键词:
- DOI:
- doi:10.5061/dryad.78qq7
- 摘要:
- demonstrates the utility of next-generation DNA sequencing technologies for QTL mapping in F1 populations, and provides a basis for the advancement of MA
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: More than one way to evolve a weed: Parallel evolution of U.S. weedy rice through independent genetic mechanisms
- 负责人:
- 关键词:
- Agricultural weeds domestication genotyping by sequencing (GBS) QTL mapping parallel evolution weedy rice
- DOI:
- doi:10.5061/dryad.566h9
- 摘要:
- e weediness traits (awn length, hull pigmentation and pericarp pigmentation), QTL mapping and sequencing of underlying candidate genes confirmed tha
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Population genomics of parallel hybrid zones in the mimetic butterflies, H. melpomene and H. erato
- 负责人:
- DOI:
- doi:10.5061/dryad.1nc50
- 摘要:
- o detect other divergent regions apparently unlinked to colour pattern differences. We also use association mapping to identify previously unmapp
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Aligner optimization increases accuracy and decreases compute times in multi-species sequence data
- 负责人:
- DOI:
- doi:10.5061/dryad.m1m0p
- 摘要:
- genomes into a single reference genome increased the specificity of mapping, while also reducing the central processing unit (CPU) time. In Plasmodium
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Genetic mapping of millions of SNPs in safflower (Carthamus tinctorius L.) via whole-genome resequencing
- 负责人:
- DOI:
- doi:10.5061/dryad.635ds
- 摘要:
- Accurate assembly of complete genomes is facilitated by very high density genetic maps. We performed low-coverage, whole-genome shotgun sequencing
![](http://agri.nais.net.cn/resources/front/images/source_91.jpg)
Data from: Scrimer: designing primers from transcriptome data
- 负责人:
- DOI:
- doi:10.5061/dryad.2p4t3
- 摘要:
- peline called Scrimer that automates multiple steps, including adaptor removal, read mapping, selection of SNPs and multiple primer design from transcriptome data