<p>The 16 genomes were sequenced on 8 Illumina HiSeq 2000 lanes. Double haploids (DHs, acc. X9748 and X9273) feature almost a double coverage compared with the other genomes; the total number of read pairs ranges from 95 Million to 207 Million. The percentage of uniquely aligning reads is evenly spread over each genome and ranges from 50 to 60% of the total. The mean coverage similarly ranges from 30 to 45X, while it is higher for the DHs.</p><p>*(JKI) Julius Kühn-Institut; (UNIBO) Università di Bologna; (WUR) Wageningen University and Research centre; (PGRU-Geneva) Plant Genetic Resources Unit; (INRA) Institut National de la Recherche Agronomique; (KUL) Katholieke Universiteit Leuven; (VNIIISPK) The All Russian Research Institute of Hortic...
Polyploidy plays an important role in the evolution of eukaryotes, especially for flower-ing plants....
Haplotypes are the units of inheritance in an organism, and many genetic analyses depend on their pr...
Polyploid organisms possess more than two copies of their core genome and therefore contain k>2 hapl...
Discovery of the DNA double helix represents one of the great milestones in biology. For plant resea...
I present the analysis on 929 high-coverage (>30x) genomes from the Human Genome Diversity Project (...
Viral haplotype reconstruction from a set of observed reads is one of the most challenging problems ...
International audienceGenome scans represent powerful approaches to investigate the action of natura...
Viral haplotype reconstruction from a set of observed reads is one of the most challenging problems ...
Background: Since the completion of the Human Genome Project in 2003, it is estimated that more than...
We report the results of an extensive investigation of genomic structures in the human genome, with ...
Genotypes from the 1000 Genomes reference [1] (v5) were intersected with HapMap3 [2] variants based ...
Premise of the study. Autopolyploidy, genome duplication within a single lineage, can result in mult...
Structural variants (SVs) are large insertions, deletions, duplications, inversions or translocation...
Improvement of variant calling in next-generation sequence data requires a comprehensive, genome-wid...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Polyploidy plays an important role in the evolution of eukaryotes, especially for flower-ing plants....
Haplotypes are the units of inheritance in an organism, and many genetic analyses depend on their pr...
Polyploid organisms possess more than two copies of their core genome and therefore contain k>2 hapl...
Discovery of the DNA double helix represents one of the great milestones in biology. For plant resea...
I present the analysis on 929 high-coverage (>30x) genomes from the Human Genome Diversity Project (...
Viral haplotype reconstruction from a set of observed reads is one of the most challenging problems ...
International audienceGenome scans represent powerful approaches to investigate the action of natura...
Viral haplotype reconstruction from a set of observed reads is one of the most challenging problems ...
Background: Since the completion of the Human Genome Project in 2003, it is estimated that more than...
We report the results of an extensive investigation of genomic structures in the human genome, with ...
Genotypes from the 1000 Genomes reference [1] (v5) were intersected with HapMap3 [2] variants based ...
Premise of the study. Autopolyploidy, genome duplication within a single lineage, can result in mult...
Structural variants (SVs) are large insertions, deletions, duplications, inversions or translocation...
Improvement of variant calling in next-generation sequence data requires a comprehensive, genome-wid...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Polyploidy plays an important role in the evolution of eukaryotes, especially for flower-ing plants....
Haplotypes are the units of inheritance in an organism, and many genetic analyses depend on their pr...
Polyploid organisms possess more than two copies of their core genome and therefore contain k>2 hapl...