A recent study on human structural variation indicates insufficiencies and errors in the human reference genome, GRCh38, and argues for the construction of a human pan-genome
The current human reference genome, GRCh38, represents over 20 years of effort to generate a high-qu...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
<div><p>The uses of the Genome Reference Consortium’s human reference sequence can be roughly catego...
A recent study on human structural variation indicates insufficiencies and errors in the human refer...
Since the completion of the human genome project, the field of genomics has relied on the human refe...
The use of the human reference genome has shaped methods and data across modern genomics. This has o...
The Human Reference Genome serves as the foundation for modern genomic analyses. However, in its pre...
Background: Structural variants comprise diverse genomic arrangements including deletions, insertion...
The current human reference genome is predominantly derived from a single individual and it does not...
<div><p>Data from the 1000 genomes project (1KGP) and Complete Genomics (CG) have dramatically incre...
The human genome reference assembly is crucial for aligning and analyzing sequence data, and for gen...
Data from the 1000 genomes project (1KGP) and Complete Genomics (CG) have dramatically increased the...
Pan-genome sequence analysis of human population ancestry is critical for expanding and better defin...
The uses of the Genome Reference Consortium’s human reference sequence can be roughly categorized in...
The alignment of sequencing reads to the reference genome is a process subject to reference bias, a ...
The current human reference genome, GRCh38, represents over 20 years of effort to generate a high-qu...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
<div><p>The uses of the Genome Reference Consortium’s human reference sequence can be roughly catego...
A recent study on human structural variation indicates insufficiencies and errors in the human refer...
Since the completion of the human genome project, the field of genomics has relied on the human refe...
The use of the human reference genome has shaped methods and data across modern genomics. This has o...
The Human Reference Genome serves as the foundation for modern genomic analyses. However, in its pre...
Background: Structural variants comprise diverse genomic arrangements including deletions, insertion...
The current human reference genome is predominantly derived from a single individual and it does not...
<div><p>Data from the 1000 genomes project (1KGP) and Complete Genomics (CG) have dramatically incre...
The human genome reference assembly is crucial for aligning and analyzing sequence data, and for gen...
Data from the 1000 genomes project (1KGP) and Complete Genomics (CG) have dramatically increased the...
Pan-genome sequence analysis of human population ancestry is critical for expanding and better defin...
The uses of the Genome Reference Consortium’s human reference sequence can be roughly categorized in...
The alignment of sequencing reads to the reference genome is a process subject to reference bias, a ...
The current human reference genome, GRCh38, represents over 20 years of effort to generate a high-qu...
The human genome reference (HGR) completion marked the genomics era beginning, yet despite its utili...
<div><p>The uses of the Genome Reference Consortium’s human reference sequence can be roughly catego...