Reference-free SNP detection: dealing with the data deluge. - Wikidata - wikimedia - TriplyDB

Reference-free SNP detection: dealing with the data deluge.

Reference-free SNP detection: dealing with the data deluge.

http://www.wikidata.org/entity/Q30838298

about

GBS-SNP-CROP: a reference-optional pipeline for SNP discovery and plant germplasm characterization using variable length, paired-end genotyping-by-sequencing data.MICADo - Looking for Mutations in Targeted PacBio Cancer Data: An Alignment-Free Method Reference-free inference of tumor phylogenies from single-cell sequencing data.Using 2k + 2 bubble searches to find single nucleotide polymorphisms in k-mer graphs.Molecular genetic diversity and population structure of Ethiopian white lupin landraces: Implications for breeding and conservation.Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data.SNP markers tightly linked to root knot nematode resistance in grapevine (Vitis cinerea) identified by a genotyping-by-sequencing approach followed by Sequenom MassARRAY validation.

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P2860

Reference-free SNP detection: dealing with the data deluge.

http://www.wikidata.org/entity/Q30838298

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Reference-free SNP detection: dealing with the data deluge.

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Dan MacLean

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P2860

Population genomics of parallel adaptation in threespine stickleback using sequenced RAD tags

An Eulerian path approach to DNA fragment assembly

De novo assembly of human genomes with massively parallel short read sequencing

Velvet: algorithms for de novo short read assembly using de Bruijn graphs

Rapid SNP discovery and genetic mapping using sequenced RAD markers

Somatic mutation, genomic variation, and neurological disease

ABySS: a parallel assembler for short read sequence data

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome

Data compression for sequencing data

Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers.

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15 Suppl 4

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Richard Leggett

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genetic variation

biomedical investigative technique

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