<p>The Jaccard similarity index is the ratio between the intersection and the union of the two sets. GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA12878 is the human genome assembly from cell line GM12878, and YH is the genome of a Han Chinese individual. For each human genome assembly, set contains all minimal absent words (MAWs) of length 11 bp, set contains all MAWs of length 50 bp, set contains all MAWs of length 100 bp, set contains all MAWs of length 300 bp, and set contains all MAWs of length 1,000 bp. The noRC columns display results without considering the reversed complement and the withRC columns display results considering the reversed complement.</p
The human reference genome assembly plays a central role in nearly all aspects of today's basic and ...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
The human genome reference assembly is crucial for aligning and analyzing sequence data, and for gen...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>GRCh37 is the reference human genome assembly build 37.1 (grey circles), HuRef is the genome of C...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>Green slices represent the fraction of A nucleotides, blue slices represent the fraction of C nuc...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>The total variation distance is defined as the normalized sum of the absolute differences between...
Minimal absent words have been computed in genomes of organisms from all domains of life. Here, we a...
Minimal absent words have been computed in genomes of organisms from all domains of life. Here, we a...
<p>Each repeat class is identified by the title of the respective subplot and subdivided into repeat...
<p>Notes: BAS, BAC, GAMMA and BANR are reference genome sets. GD is genome distance. Scaling factor ...
<p>(<b>A</b>) The average similarity in KO content between each reconstructed genus and sequenced ge...
The human reference genome assembly plays a central role in nearly all aspects of today's basic and ...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
The human genome reference assembly is crucial for aligning and analyzing sequence data, and for gen...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>GRCh37 is the reference human genome assembly build 37.1 (grey circles), HuRef is the genome of C...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>Green slices represent the fraction of A nucleotides, blue slices represent the fraction of C nuc...
<p>GRCh37 is the reference human genome assembly build 37.1, HuRef is the genome of Craig Venter, NA...
<p>The total variation distance is defined as the normalized sum of the absolute differences between...
Minimal absent words have been computed in genomes of organisms from all domains of life. Here, we a...
Minimal absent words have been computed in genomes of organisms from all domains of life. Here, we a...
<p>Each repeat class is identified by the title of the respective subplot and subdivided into repeat...
<p>Notes: BAS, BAC, GAMMA and BANR are reference genome sets. GD is genome distance. Scaling factor ...
<p>(<b>A</b>) The average similarity in KO content between each reconstructed genus and sequenced ge...
The human reference genome assembly plays a central role in nearly all aspects of today's basic and ...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
The human genome reference assembly is crucial for aligning and analyzing sequence data, and for gen...