Pages that link to "Q34241652"

The following pages link to Segmental duplications: what's missing, misassigned, and misassembled--and should we care? (Q34241652):

Displaying 50 items.

• Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Q22122498) (← links)
• DUF1220 domains, cognitive disease, and human brain evolution (Q22337096) (← links)
• Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure (Q24561845) (← links)
• Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication (Q24614384) (← links)
• Phylogenomic approaches to common problems encountered in the analysis of low copy repeats: the sulfotransferase 1A gene family example (Q24804582) (← links)
• Hotspots of homologous recombination in the human genome: not all homologous sequences are equal (Q24809343) (← links)
• Rapid expansion and functional divergence of subtelomeric gene families in yeasts. (Q27937316) (← links)
• Divergent origins and concerted expansion of two segmental duplications on chromosome 16 (Q28214407) (← links)
• Evolutionary-new centromeres preferentially emerge within gene deserts (Q28755361) (← links)
• THE COMPLEX STRUCTURE AND DYNAMIC EVOLUTION OF HUMAN SUBTELOMERES (Q29393384) (← links)
• Genome architecture, rearrangements and genomic disorders (Q29614721) (← links)
• Mechanisms for Structural Variation in the Human Genome (Q30412742) (← links)
• Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome (Q30434301) (← links)
• The genomic distribution of intraspecific and interspecific sequence divergence of human segmental duplications relative to human/chimpanzee chromosomal rearrangements (Q30847205) (← links)
• Analysis of recent segmental duplications in the bovine genome (Q30936634) (← links)
• Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry (Q33183872) (← links)
• Characterization of the segmental duplication LCR7-20 in the human genome (Q33196471) (← links)
• The jewels of our genome: the search for the genomic changes underlying the evolutionarily unique capacities of the human brain (Q33245079) (← links)
• Database of Trypanosoma cruzi repeated genes: 20,000 additional gene variants (Q33304033) (← links)
• Characterization of genome-wide segmental duplications reveals a common genomic feature of association with immunity among domestic animals (Q33556209) (← links)
• A critical assessment of cross-species detection of gene duplicates using comparative genomic hybridization (Q33577478) (← links)
• Inversion variants in the human genome: role in disease and genome architecture (Q33762256) (← links)
• Segmental duplications: evolution and impact among the current Lepidoptera genomes (Q33877529) (← links)
• Genome architecture catalyzes nonrecurrent chromosomal rearrangements (Q33904646) (← links)
• The evolution of human segmental duplications and the core duplicon hypothesis (Q33965283) (← links)
• Recent duplication, domain accretion and the dynamic mutation of the human genome (Q34098904) (← links)
• Refinement of Bos taurus sequence assembly based on BAC-FISH experiments. (Q34114434) (← links)
• Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene (Q34130421) (← links)
• The evolution of morphological complexity in zebrafish stripes (Q34540784) (← links)
• Molecular-evolutionary mechanisms for genomic disorders (Q34699430) (← links)
• Segmental duplications in the silkworm genome (Q34882665) (← links)
• Computational comparison of human genomic sequence assemblies for a region of chromosome 4. (Q35004232) (← links)
• Vertebrate evolution: doubling and shuffling with a full deck (Q35031134) (← links)
• High-density single-nucleotide polymorphism maps of the human genome. (Q35828010) (← links)
• A model of segmental duplication formation in Drosophila melanogaster (Q36004644) (← links)
• Duplication, coclustering, and selection of human Alu retrotransposons (Q36017653) (← links)
• Array comparative genomic hybridization and its applications in cancer (Q36141621) (← links)
• Between-species differences in gene copy number are enriched among functions critical for adaptive evolution in Arabidopsis halleri (Q36268721) (← links)
• Evolutionary analysis of heterochromatin protein compatibility by interspecies complementation in Saccharomyces (Q36466270) (← links)
• A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture (Q36474818) (← links)
• Analysis of segmental duplications and genome assembly in the mouse (Q36684896) (← links)
• Genomic rearrangements and sporadic disease (Q36863512) (← links)
• Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and females (Q37203101) (← links)
• Recent segmental duplications in the working draft assembly of the brown Norway rat. (Q37322204) (← links)
• CpG methylation modifies the genetic stability of cloned repeat sequences (Q39860943) (← links)
• Personalized evolutionary hypothesis in genomics and auxiliary lymph node through diverse subtelomeric signal profile (Q41491479) (← links)
• Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues. (Q42154820) (← links)
• Discovery of the human genome sequence in the public and private databases (Q48336582) (← links)
• The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3 (Q52097958) (← links)
• Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family. (Q52312110) (← links)