<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ebert, Peter</style></author><author><style face="normal" font="default" size="100%">Audano, Peter A</style></author><author><style face="normal" font="default" size="100%">Zhu, Qihui</style></author><author><style face="normal" font="default" size="100%">Rodriguez-Martin, Bernardo</style></author><author><style face="normal" font="default" size="100%">Porubsky, David</style></author><author><style face="normal" font="default" size="100%">Bonder, Marc Jan</style></author><author><style face="normal" font="default" size="100%">Sulovari, Arvis</style></author><author><style face="normal" font="default" size="100%">Ebler, Jana</style></author><author><style face="normal" font="default" size="100%">Zhou, Weichen</style></author><author><style face="normal" font="default" size="100%">Serra Mari, Rebecca</style></author><author><style face="normal" font="default" size="100%">Yilmaz, Feyza</style></author><author><style face="normal" font="default" size="100%">Zhao, Xuefang</style></author><author><style face="normal" font="default" size="100%">Hsieh, PingHsun</style></author><author><style face="normal" font="default" size="100%">Lee, Joyce</style></author><author><style face="normal" font="default" size="100%">Kumar, Sushant</style></author><author><style face="normal" font="default" size="100%">Lin, Jiadong</style></author><author><style face="normal" font="default" size="100%">Rausch, Tobias</style></author><author><style face="normal" font="default" size="100%">Chen, Yu</style></author><author><style face="normal" font="default" size="100%">Ren, Jingwen</style></author><author><style face="normal" font="default" size="100%">Santamarina, Martin</style></author><author><style face="normal" font="default" size="100%">Höps, Wolfram</style></author><author><style face="normal" font="default" size="100%">Ashraf, Hufsah</style></author><author><style face="normal" font="default" size="100%">Chuang, Nelson T</style></author><author><style face="normal" font="default" size="100%">Yang, Xiaofei</style></author><author><style face="normal" font="default" size="100%">Munson, Katherine M</style></author><author><style face="normal" font="default" size="100%">Lewis, Alexandra P</style></author><author><style face="normal" font="default" size="100%">Fairley, Susan</style></author><author><style face="normal" font="default" size="100%">Tallon, Luke J</style></author><author><style face="normal" font="default" size="100%">Clarke, Wayne E</style></author><author><style face="normal" font="default" size="100%">Basile, Anna O</style></author><author><style face="normal" font="default" size="100%">Byrska-Bishop, Marta</style></author><author><style face="normal" font="default" size="100%">Corvelo, André</style></author><author><style face="normal" font="default" size="100%">Evani, Uday S</style></author><author><style face="normal" font="default" size="100%">Lu, Tsung-Yu</style></author><author><style face="normal" font="default" size="100%">Chaisson, Mark J P</style></author><author><style face="normal" font="default" size="100%">Chen, Junjie</style></author><author><style face="normal" font="default" size="100%">Li, Chong</style></author><author><style face="normal" font="default" size="100%">Brand, Harrison</style></author><author><style face="normal" font="default" size="100%">Wenger, Aaron M</style></author><author><style face="normal" font="default" size="100%">Ghareghani, Maryam</style></author><author><style face="normal" font="default" size="100%">Harvey, William T</style></author><author><style face="normal" font="default" size="100%">Raeder, Benjamin</style></author><author><style face="normal" font="default" size="100%">Hasenfeld, Patrick</style></author><author><style face="normal" font="default" size="100%">Regier, Allison A</style></author><author><style face="normal" font="default" size="100%">Abel, Haley J</style></author><author><style face="normal" font="default" size="100%">Hall, Ira M</style></author><author><style face="normal" font="default" size="100%">Flicek, Paul</style></author><author><style face="normal" font="default" size="100%">Stegle, Oliver</style></author><author><style face="normal" font="default" size="100%">Gerstein, Mark B</style></author><author><style face="normal" font="default" size="100%">Tubio, Jose M C</style></author><author><style face="normal" font="default" size="100%">Mu, Zepeng</style></author><author><style face="normal" font="default" size="100%">Li, Yang I</style></author><author><style face="normal" font="default" size="100%">Shi, Xinghua</style></author><author><style face="normal" font="default" size="100%">Hastie, Alex R</style></author><author><style face="normal" font="default" size="100%">Ye, Kai</style></author><author><style face="normal" font="default" size="100%">Chong, Zechen</style></author><author><style face="normal" font="default" size="100%">Sanders, Ashley D</style></author><author><style face="normal" font="default" size="100%">Zody, Michael C</style></author><author><style face="normal" font="default" size="100%">Talkowski, Michael E</style></author><author><style face="normal" font="default" size="100%">Mills, Ryan E</style></author><author><style face="normal" font="default" size="100%">Devine, Scott E</style></author><author><style face="normal" font="default" size="100%">Lee, Charles</style></author><author><style face="normal" font="default" size="100%">Korbel, Jan O</style></author><author><style face="normal" font="default" size="100%">Marschall, Tobias</style></author><author><style face="normal" font="default" size="100%">Eichler, Evan E</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Haplotype-resolved diverse human genomes and integrated analysis of structural variation.</style></title><secondary-title><style face="normal" font="default" size="100%">Science</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Science</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Female</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic Variation</style></keyword><keyword><style  face="normal" font="default" size="100%">Genome, Human</style></keyword><keyword><style  face="normal" font="default" size="100%">Genotype</style></keyword><keyword><style  face="normal" font="default" size="100%">Haplotypes</style></keyword><keyword><style  face="normal" font="default" size="100%">High-Throughput Nucleotide Sequencing</style></keyword><keyword><style  face="normal" font="default" size="100%">Humans</style></keyword><keyword><style  face="normal" font="default" size="100%">INDEL Mutation</style></keyword><keyword><style  face="normal" font="default" size="100%">Interspersed Repetitive Sequences</style></keyword><keyword><style  face="normal" font="default" size="100%">Male</style></keyword><keyword><style  face="normal" font="default" size="100%">Population Groups</style></keyword><keyword><style  face="normal" font="default" size="100%">Quantitative Trait Loci</style></keyword><keyword><style  face="normal" font="default" size="100%">Retroelements</style></keyword><keyword><style  face="normal" font="default" size="100%">Sequence Analysis, DNA</style></keyword><keyword><style  face="normal" font="default" size="100%">Sequence Inversion</style></keyword><keyword><style  face="normal" font="default" size="100%">Whole Genome Sequencing</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021 04 02</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">372</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Long-read and strand-specific sequencing technologies together facilitate the de novo assembly of high-quality haplotype-resolved human genomes without parent-child trio data. We present 64 assembled haplotypes from 32 diverse human genomes. These highly contiguous haplotype assemblies (average minimum contig length needed to cover 50% of the genome: 26 million base pairs) integrate all forms of genetic variation, even across complex loci. We identified 107,590 structural variants (SVs), of which 68% were not discovered with short-read sequencing, and 278 SV hotspots (spanning megabases of gene-rich sequence). We characterized 130 of the most active mobile element source elements and found that 63% of all SVs arise through homology-mediated mechanisms. This resource enables reliable graph-based genotyping from short reads of up to 50,340 SVs, resulting in the identification of 1526 expression quantitative trait loci as well as SV candidates for adaptive selection within the human population.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">6537</style></issue><custom1><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/33632895?dopt=Abstract</style></custom1></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Weissensteiner, Matthias H</style></author><author><style face="normal" font="default" size="100%">Bunikis, Ignas</style></author><author><style face="normal" font="default" size="100%">Catalán, Ana</style></author><author><style face="normal" font="default" size="100%">Francoijs, Kees-Jan</style></author><author><style face="normal" font="default" size="100%">Knief, Ulrich</style></author><author><style face="normal" font="default" size="100%">Heim, Wieland</style></author><author><style face="normal" font="default" size="100%">Peona, Valentina</style></author><author><style face="normal" font="default" size="100%">Pophaly, Saurabh D</style></author><author><style face="normal" font="default" size="100%">Sedlazeck, Fritz J</style></author><author><style face="normal" font="default" size="100%">Suh, Alexander</style></author><author><style face="normal" font="default" size="100%">Warmuth, Vera M</style></author><author><style face="normal" font="default" size="100%">Wolf, Jochen B W</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Discovery and population genomics of structural variation in a songbird genus.</style></title><secondary-title><style face="normal" font="default" size="100%">Nat Commun</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nat Commun</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Animals</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromosome Inversion</style></keyword><keyword><style  face="normal" font="default" size="100%">Gene Deletion</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic Variation</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetics, Population</style></keyword><keyword><style  face="normal" font="default" size="100%">Genome</style></keyword><keyword><style  face="normal" font="default" size="100%">Genomic Structural Variation</style></keyword><keyword><style  face="normal" font="default" size="100%">Genotype</style></keyword><keyword><style  face="normal" font="default" size="100%">Phylogeny</style></keyword><keyword><style  face="normal" font="default" size="100%">Polymorphism, Single Nucleotide</style></keyword><keyword><style  face="normal" font="default" size="100%">Retroelements</style></keyword><keyword><style  face="normal" font="default" size="100%">Sequence Analysis, DNA</style></keyword><keyword><style  face="normal" font="default" size="100%">Songbirds</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020 07 07</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">3403</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Structural variation (SV) constitutes an important type of genetic mutations providing the raw material for evolution. Here, we uncover the genome-wide spectrum of intra- and interspecific SV segregating in natural populations of seven songbird species in the genus Corvus. Combining short-read (N = 127) and long-read re-sequencing (N = 31), as well as optical mapping (N = 16), we apply both assembly- and read mapping approaches to detect SV and characterize a total of 220,452 insertions, deletions and inversions. We exploit sampling across wide phylogenetic timescales to validate SV genotypes and assess the contribution of SV to evolutionary processes in an avian model of incipient speciation. We reveal an evolutionary young (~530,000 years) cis-acting 2.25-kb LTR retrotransposon insertion reducing expression of the NDP gene with consequences for premating isolation. Our results attest to the wealth and evolutionary significance of SV segregating in natural populations and highlight the need for reliable SV genotyping.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><custom1><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/32636372?dopt=Abstract</style></custom1></record></records></xml>