ENGINES: exploring single nucleotide variation in entire human genomes
about
Mitogenomes from The 1000 Genome Project reveal new Near Eastern features in present-day TuscansUniparental markers of contemporary Italian population reveals details on its pre-Roman heritageSInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence dataInference of Ancestry in Forensic Analysis II: Analysis of Genetic Data.Evaluating the accuracy of AIM panels at quantifying genome ancestryKaviar: an accessible system for testing SNV novelty.Exomic sequencing of immune-related genes reveals novel candidate variants associated with alopecia universalis.The cyclic AMP pathway is a sex-specific modifier of glioma risk in type I neurofibromatosis patients.A genome-wide study of modern-day Tuscans: revisiting Herodotus's theory on the origin of the Etruscans.Age-associated DNA methylation changes in immune genes, histone modifiers and chromatin remodeling factors within 5 years after birth in human blood leukocytesHuvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection.Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies.1000 Genomes Selection Browser 1.0: a genome browser dedicated to signatures of natural selection in modern humans.Fine-mapping of IL16 gene and prostate cancer risk in African Americans.Whole Exome Sequencing reveals new candidate genes in host genomic susceptibility to Respiratory Syncytial Virus Disease.An SNP panel for the analysis of paternally inherited alleles in maternal plasma using ion Torrent PGM.Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.Whole Exome Sequencing Identifies New Host Genomic Susceptibility Factors in Empyema Caused by Streptococcus pneumoniae in Children: A Pilot Study.
P2860
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P2860
ENGINES: exploring single nucleotide variation in entire human genomes
description
2011 nî lūn-bûn
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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年論文
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2011年論文
@zh-hant
2011年論文
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2011年論文
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2011年論文
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2011年论文
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ENGINES: exploring single nucleotide variation in entire human genomes
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ENGINES: exploring single nucleotide variation in entire human genomes
@en
ENGINES: exploring single nucleotide variation in entire human genomes
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label
ENGINES: exploring single nucleotide variation in entire human genomes
@ast
ENGINES: exploring single nucleotide variation in entire human genomes
@en
ENGINES: exploring single nucleotide variation in entire human genomes
@nl
prefLabel
ENGINES: exploring single nucleotide variation in entire human genomes
@ast
ENGINES: exploring single nucleotide variation in entire human genomes
@en
ENGINES: exploring single nucleotide variation in entire human genomes
@nl
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ENGINES: exploring single nucleotide variation in entire human genomes
@en
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10.1186/1471-2105-12-105
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2011-04-19T00:00:00Z
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1011213284