<p>Numbers shown are average numbers per individual except where indicated otherwise.</p>1<p>For autosomes only; <sup>2</sup> 1000 G_LC: Low-coverage samples from the 1000 Genomes Project; <sup>3</sup> 1000 G_HCT: High-coverage trios from the 1000 Genomes Project.</p
A 2.91-billion base pair (bp) consensus sequence of the euchromatic portion of the human genome was ...
A) Histogram of 1,035 whole-genome sequencing (WGS) samples from APIC and URECA by mean depth of cov...
<p>(A-E) Comparison of personal genome enrichments of 1,094 genomes from the 1,000 genomes project a...
<p>Data is averaged across all sample lanes within the given ranges of human DNA quantities. On aver...
Summary of analyses done on whole genome sequences involving 1616 genomes in different phyla that ex...
While it is easy to assume that whole-genome sequencing (WGS) involves sequencing each base in a gen...
Each point indicates the per-bp rate of archaic coverage on autosomes and chromosome X in a global h...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
<p>Basic genome statistics for genome DNA sequences. Values of zero are marked by “−”. Abbreviations...
Coverage is the per-base pair proportion of the genome inferred to have come from archaic sources, f...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
1000 individuals in an effort to produce the most complete catalog of human genetic variation to dat...
Background: Since the completion of the Human Genome Project in 2003, it is estimated that more than...
<p>Summary of sequencing results including the average read-depth, number of reads and mutations det...
<p>There isn't a great deal of summary statistics data available on human-specific sequencing data. ...
A 2.91-billion base pair (bp) consensus sequence of the euchromatic portion of the human genome was ...
A) Histogram of 1,035 whole-genome sequencing (WGS) samples from APIC and URECA by mean depth of cov...
<p>(A-E) Comparison of personal genome enrichments of 1,094 genomes from the 1,000 genomes project a...
<p>Data is averaged across all sample lanes within the given ranges of human DNA quantities. On aver...
Summary of analyses done on whole genome sequences involving 1616 genomes in different phyla that ex...
While it is easy to assume that whole-genome sequencing (WGS) involves sequencing each base in a gen...
Each point indicates the per-bp rate of archaic coverage on autosomes and chromosome X in a global h...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
<p>Basic genome statistics for genome DNA sequences. Values of zero are marked by “−”. Abbreviations...
Coverage is the per-base pair proportion of the genome inferred to have come from archaic sources, f...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
1000 individuals in an effort to produce the most complete catalog of human genetic variation to dat...
Background: Since the completion of the Human Genome Project in 2003, it is estimated that more than...
<p>Summary of sequencing results including the average read-depth, number of reads and mutations det...
<p>There isn't a great deal of summary statistics data available on human-specific sequencing data. ...
A 2.91-billion base pair (bp) consensus sequence of the euchromatic portion of the human genome was ...
A) Histogram of 1,035 whole-genome sequencing (WGS) samples from APIC and URECA by mean depth of cov...
<p>(A-E) Comparison of personal genome enrichments of 1,094 genomes from the 1,000 genomes project a...