SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries. - Wikidata - awgldk - TriplyDB

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries.

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries.

http://www.wikidata.org/entity/Q33320976

about

Genotyping-by-sequencing for Populus population genomics: an assessment of genome sampling patterns and filtering approaches Double digest RADseq: an inexpensive method for de novo SNP discovery and genotyping in model and non-model species The origin and evolution of lactation Generation of SNP datasets for orangutan population genomics using improved reduced-representation sequencing and direct comparisons of SNP calling algorithms.A genome-wide survey of genetic variation in gorillas using reduced representation sequencing High-throughput SNP genotyping in the highly heterozygous genome of Eucalyptus: assay success, polymorphism and transferability across species Sequencing technologies and genome sequencing Harnessing the power of RADseq for ecological and evolutionary genomics Genome Wide Sampling Sequencing for SNP Genotyping: Methods, Challenges and Future Development A field guide to whole-genome sequencing, assembly and annotation Genomic Variants Revealed by Invariably Missing Genotypes in Nelore Cattle Genotyping-by-sequencing (GBS): a novel, efficient and cost-effective genotyping method for cattle using next-generation sequencing Development and characterization of a high density SNP genotyping assay for cattle Genotyping by sequencing approaches to characterise crop genomes: choosing the right tool for the right application Rapid SNP discovery and genetic mapping using sequenced RAD markers New World cattle show ancestry from multiple independent domestication events Quantitative trait locus analysis of body shape divergence in nine-spined sticklebacks based on high-density SNP-panel The use of museum specimens with high-throughput DNA sequencers Comparative transcriptome analysis of two oysters, Crassostrea gigas and Crassostrea hongkongensis provides insights into adaptation to hypo-osmotic conditions Genome-wide analysis reveals the ancient and recent admixture history of East African Shorthorn Zebu from Western Kenya Single Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) Data Comparative species divergence across eight triplets of spiny lizards (Sceloporus) using genomic sequence data Two different high throughput sequencing approaches identify thousands of de novo genomic markers for the genetically depleted Bornean elephant Genomic diversity in switchgrass (Panicum virgatum): from the continental scale to a dune landscape Sequence-based genotyping for marker discovery and co-dominant scoring in germplasm and populations Evolution of the bovine TLR gene family and member associations with Mycobacterium avium subspecies paratuberculosis infection A reduced representation approach to population genetic analyses and applications to human evolution Genome-wide polymorphism and comparative analyses in the white-tailed deer (Odocoileus virginianus): a model for conservation genomics Applications of next generation sequencing in molecular ecology of non-model organisms Resolving the evolution of extant and extinct ruminants with high-throughput phylogenomics Identification of SNPs in a nonmodel macrofungus (Lepista nuda, Basidiomycota) through RAD sequencing Genomics-assisted characterization of a breeding collection of Apios americana, an edible tuberous legume CNV-seq, a new method to detect copy number variation using high-throughput sequencing RESTseq--efficient benchtop population genomics with RESTriction Fragment SEQuencing Whole-genome resequencing shows numerous genes with nonsynonymous SNPs in the Japanese native cattle Kuchinoshima-Ushi.SNPchiMp: a database to disentangle the SNPchip jungle in bovine livestock Dissecting structural and nucleotide genome-wide variation in inbred Iberian pigs.LDx: estimation of linkage disequilibrium from high-throughput pooled resequencing data.Genomic prediction in animals and plants: simulation of data, validation, reporting, and benchmarking Impact of the next-generation sequencing data depth on various biological result inferences.

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P2860

SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries.

http://www.wikidata.org/entity/Q33320976

description

2008 nî lūn-bûn

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2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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2008年论文

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name

SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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type

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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SNP discovery and allele frequ ...... uced representation libraries.

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Christian D Haudenschild

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Cynthia Taylor Lawley

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Jeremy F Taylor

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Lakshmi K Matukumalli

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Stephen S Moore

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Tad S Sonstegard

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Timothy P L Smith

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Wesley C Warren

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P2860

Genome sequence, comparative analysis and haplotype structure of the domestic dog

Complement factor H polymorphism in age-related macular degeneration

A haplotype map of the human genome

SNP discovery via 454 transcriptome sequencing

The International HapMap Project

A genome-wide association study identifies novel risk loci for type 2 diabetes

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

Genome-wide mapping of in vivo protein-DNA interactions

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

An SNP map of the human genome generated by reduced representation shotgun sequencing.

P2888

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247-252

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scholarly article

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10.1038/NMETH.1185

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3

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5

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Robert D. Schnabel

Curtis P Van Tassell

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2008-02-24T00:00:00Z

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5555304

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1034942023

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18297082

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