Deep sequencing of 10,000 human genomes - Wikidata - awgldk - TriplyDB

Deep sequencing of 10,000 human genomes

Deep sequencing of 10,000 human genomes

http://www.wikidata.org/entity/Q27133767

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Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data Prediction of harmful variants on mitochondrial genes: Test of habitat-dependent and demographic effects in a euryhaline fish.Sequencing and de novo assembly of 150 genomes from Denmark as a population reference ReliableGenome: annotation of genomic regions with high/low variant calling concordance.The blood DNA virome in 8,000 humans.The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.Reliability of algorithmic somatic copy number alteration detection from targeted capture data.It takes a genome to understand a village: Population scale precision medicine.SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.The Mobile Element Locator Tool (MELT): Population-scale mobile element discovery and biology.Biological function in the twilight zone of sequence conservation Big data opens a window onto wellness.Reference standards for next-generation sequencing.Fast and accurate HLA typing from short-read next-generation sequence data with xHLA.Challenges and Opportunities in Linking Long Noncoding RNAs to Cardiovascular, Lung, and Blood Diseases.Penetrance and the Healthy Elderly.Identification of individuals by trait prediction using whole-genome sequencing data.Fine population structure analysis method for genomes of many.Cloud-based Interactive Analytics for Terabytes of Genomic Variants Data.Human gene essentiality.Interpreting short tandem repeat variations in humans using mutational constraint.Genetics and the conservation of natural populations: allozymes to genomes.New Insights into the Genetic Basis of Monge's Disease and Adaptation to High-Altitude.Lightning-fast genome variant detection with GROM.A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes.Deleterious variants in DCHS1 are prevalent in sporadic cases of mitral valve prolapse.CoVaCS: a consensus variant calling system.High-throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders.Acetaminophen (Paracetamol) Use Modifies the Sulfation of Sex Hormones.Genetic risk, dysbiosis, and treatment stratification using host genome and gut microbiome in inflammatory bowel disease.Digital Twins in Health Care: Ethical Implications of an Emerging Engineering Paradigm.Genetic variants in mRNA untranslated regions.Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.KoVariome: Korean National Standard Reference Variome database of whole genomes with comprehensive SNV, indel, CNV, and SV analyses.Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults.Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study.Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters.The fecal metabolome as a functional readout of the gut microbiome De novo human genome assemblies reveal spectrum of alternative haplotypes in diverse populations

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Deep sequencing of 10,000 human genomes

http://www.wikidata.org/entity/Q27133767

description

2016 nî lūn-bûn

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2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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name

Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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Deep sequencing of 10,000 human genomes

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PNAS.1613365113

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Deep sequencing of 10,000 human genomes

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P2093

Ahmed Moustafa

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Brad A Perkins

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Chad Garner

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Chao Xie

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Efren Sandoval

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Emily H M Wong

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Ewen F Kirkness

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Franz J Och

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Gary Metzker

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Levi C T Pierce

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P2860

Medical implications of technical accuracy in genome sequencing

A global reference for human genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

Extensive sequencing of seven human genomes to characterize benchmark reference materials.

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium

Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals

An expanded sequence context model broadly explains variability in polymorphism levels across the human genome

A general framework for estimating the relative pathogenicity of human genetic variants

Genome-scale CRISPR-Cas9 knockout screening in human cells

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11901-11906

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scholarly article

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10.1073/PNAS.1613365113

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J. Craig Venter

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2016-10-18T00:00:00Z

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27702888

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5081584

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