About: covid:PMC5499171

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About: covid:PMC5499171 Goto Sponge NotDistinct Permalink

An Entity of Type : owl:Thing, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
Creator	McMillan, Leonard Hock, Pablo Kashfeen, Anwica Sullivan, Patrick Ferris, Martin Morgan, Andrew Giusti-Rodríguez, Paola Srivastava, Anuj Bell, Timothy Churchill, Gary McMullan, Rachel Miller, Darla Najarian, Maya Sarsani, Vishal Shorter, John Sigmon, J. Williams, Lucy de Villena, Fernando
is schema:about of	named entity 'Collaborative' named entity 'NYGC' named entity 'recombination' named entity 'median absolute deviation' named entity 'genome' named entity 'chromosome' named entity 'copy number' named entity 'genotypes' named entity 'PCR' named entity 'genotyping' named entity 'QTL' named entity 'hemizygous' named entity 'Illumina' named entity 'genome sequencing' named entity 'copy number' named entity 'deletions' named entity 'heterozygous' named entity 'gene expression' named entity 'New York Genome Center' named entity 'homozygous' named entity 'sequence data' named entity 'mitochondria' named entity 'indels' named entity 'k-mer' named entity 'autosomal' named entity 'SNPs' named entity 'High Throughput Sequencing' named entity 'epistatic' named entity 'Keane' named entity 'inbreeding' named entity 'haplotype' named entity 'mitochondria' named entity 'genotyping arrays' named entity 'genotyped' named entity 'Ploidy' named entity 'VCF' named entity 'chromosome' named entity 'RNA' named entity 'chromosome' named entity 'genotyping' named entity 'inbreeding' named entity 'genotyping' named entity 'open reading frame' named entity 'chromosome' named entity 'SNPs' named entity 'phenotypes' named entity 'indels' named entity 'heterozygosity' named entity 'Ensembl' named entity 'Sanger Institute' named entity 'ultrasonication' named entity 'genome' named entity 'haplotype' named entity 'polymorphism' named entity 'haplotypes' named entity 'genotypes' named entity 'locus' named entity 'indel' named entity 'genome' named entity 'loci' named entity 'loci' named entity 'forward-backward algorithm' named entity 'SNPs' named entity 'genotyping platforms' named entity 'recombinant inbred strain' named entity 'primers' named entity 'Illumina sequencing' named entity 'autosomal' named entity 'genomes' named entity 'genotypes' named entity 'locus' named entity 'genomes' named entity 'haplotype' named entity 'coding region' named entity 'deletions' named entity 'homozygous' named entity 'genome sequences' named entity 'Keane' named entity 'haplotype' named entity 'Woburn' named entity 'chromosome' named entity 'SQLite'

Attributes

Values

Creator

McMillan, Leonard
Hock, Pablo
Kashfeen, Anwica
Sullivan, Patrick
Ferris, Martin
Morgan, Andrew
Giusti-Rodríguez, Paola
Srivastava, Anuj
Bell, Timothy
Churchill, Gary
McMullan, Rachel
Miller, Darla
Najarian, Maya
Sarsani, Vishal
Shorter, John
Sigmon, J.
Williams, Lucy
de Villena, Fernando

is schema:about of

named entity 'Collaborative'
named entity 'NYGC'
named entity 'recombination'
named entity 'median absolute deviation'
named entity 'genome'
named entity 'chromosome'
named entity 'copy number'
named entity 'genotypes'
named entity 'PCR'
named entity 'genotyping'
named entity 'QTL'
named entity 'hemizygous'
named entity 'Illumina'
named entity 'genome sequencing'
named entity 'copy number'
named entity 'deletions'
named entity 'heterozygous'
named entity 'gene expression'
named entity 'New York Genome Center'
named entity 'homozygous'
named entity 'sequence data'
named entity 'mitochondria'
named entity 'indels'
named entity 'k-mer'
named entity 'autosomal'
named entity 'SNPs'
named entity 'High Throughput Sequencing'
named entity 'epistatic'
named entity 'Keane'
named entity 'inbreeding'
named entity 'haplotype'
named entity 'mitochondria'
named entity 'genotyping arrays'
named entity 'genotyped'
named entity 'Ploidy'
named entity 'VCF'
named entity 'chromosome'
named entity 'RNA'
named entity 'chromosome'
named entity 'genotyping'
named entity 'inbreeding'
named entity 'genotyping'
named entity 'open reading frame'
named entity 'chromosome'
named entity 'SNPs'
named entity 'phenotypes'
named entity 'indels'
named entity 'heterozygosity'
named entity 'Ensembl'
named entity 'Sanger Institute'
named entity 'ultrasonication'
named entity 'genome'
named entity 'haplotype'
named entity 'polymorphism'
named entity 'haplotypes'
named entity 'genotypes'
named entity 'locus'
named entity 'indel'
named entity 'genome'
named entity 'loci'
named entity 'loci'
named entity 'forward-backward algorithm'
named entity 'SNPs'
named entity 'genotyping platforms'
named entity 'recombinant inbred strain'
named entity 'primers'
named entity 'Illumina sequencing'
named entity 'autosomal'
named entity 'genomes'
named entity 'genotypes'
named entity 'locus'
named entity 'genomes'
named entity 'haplotype'
named entity 'coding region'
named entity 'deletions'
named entity 'homozygous'
named entity 'genome sequences'
named entity 'Keane'
named entity 'haplotype'
named entity 'Woburn'
named entity 'chromosome'
named entity 'SQLite'

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